UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
Washington,
D.C. 20549
FORM
10-Q
☑ | Quarterly report pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 |
| For the quarterly period ended December 31, 2024 |
| |
☐ | Transition report pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 |
Commission
file number: 001-32830

IGC
PHARMA, INC.
(Exact
name of registrant as specified in its charter)
Maryland | | 20-2760393 |
(State or other jurisdiction of incorporation or organization) | | (I.R.S. Employer Identification No.) |
| | |
10224 Falls Road, Potomac, Maryland | | 20854 |
(Address of principal executive offices) | | (Zip Code) |
(301)
983-0998
(Registrant’s
telephone number, including area code)
Securities
registered pursuant to Section 12(b) of the Act:
Not
Applicable
(Former
name, former address and former fiscal year, if changed since last report.)
Title of each class | | Trading symbol(s) | | Name of each exchange on which registered |
Common Stock, par value $0.0001 per share | | IGC | | NYSE American LLC |
Indicate
by check mark whether the registrant: (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange
Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2)
has been subject to such filing requirements for the past 90 days. ☑ Yes ☐ No
Indicate
by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule
405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant
was required to submit such files). ☑ Yes ☐ No
Indicate
by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting
company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,”
“smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.
Large accelerated filer ☐ | Accelerated filer ☐ |
Non-accelerated filer ☑ | Smaller reporting company ☑ |
| Emerging growth company☐ |
If
an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying
with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Indicate
by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). ☐ Yes ☑ No
79,685,165
shares of our common stock were outstanding as of February 10, 2025.
IGC
PHARMA, INC.
FORM
10-Q
FOR
THE QUARTERLY PERIOD ENDED DECEMBER 31, 2024
|
|
December 31, 2024, Form 10-Q |
FORWARD-LOOKING
STATEMENTS
This
Quarterly Report on Form 10-Q and the documents incorporated herein by reference contain “forward-looking statements.”
Additionally, we, or our representatives, may, from time to time, make other written or verbal forward-looking statements and discuss
plans, expectations, and objectives regarding our business, financial condition, and results of operations. Without limiting the foregoing,
statements that are in the future tense, and all statements accompanied by terms such as “believe,” “hope,”
“potential,” “project,” “expect,” “trend,” “estimate,”
“forecast,” “assume,” “intend,” “plan,” “target,”
“anticipate,” “outlook,” “preliminary,” “will likely result,”
“will continue,” and variations of them and similar terms are intended to be forward-looking statements”
as defined by federal securities laws. Such statements are based on currently available information, which management has assessed
but which is dynamic and subject to rapid change due to risks and uncertainties that affect our business.
For
the next several years, we believe our success is highly correlated with the outcome of our clinical trials and secondarily with the
sale of our products and services. The Company may not be able to complete human trials on our investigational drug candidates, or, once
conducted, the results of human trials may not be favorable or as anticipated or may reflect a lack of efficacy in humans or animals.
Precautions, including social distancing and travel restrictions, among others could lead to delays or expenses greater than anticipated
or projected. Failure or delay with respect to any of the above factors could have a material adverse effect on our business, future
results of operations, stock price, and financial condition.
Our
projections and investments anticipate certain regulatory changes and stable pricing, which may not hold out over the next several years.
We may not be able to protect our intellectual property adequately or receive patents. We may not receive regulatory approval for our
products or trials. The patent applications we have licensed may not be granted by the United States Patent and Trademark Office (“USPTO”),
even if the Company is in full compliance with USPTO requirements. We may not have adequate resources, including financial resources,
to successfully conduct all requisite clinical trials, to bring a product based on the above-referenced patented formulations to market,
or to pay applicable maintenance fees over time. We may not be able to successfully commercialize our products even if they are successful
and receive regulatory approval, including, but not limited to, based on the Food and Drug Administration’s (“FDA”)
current position on hemp and hemp-based products. Failure or delay with respect to any of the factors above could have a material adverse
effect on our business, future results of operations, stock price, and financial condition.
This
document also contains statements that are not approved by the FDA, including but not limited to the statements on hemp and hemp extracts
and their potential efficacy on humans and animals. While these statements and claims are intended to be in compliance with federal and
state laws, we cannot guarantee such compliance.
We
caution you not to place undue reliance on forward-looking statements, which are based upon assumptions, expectations, plans, and projections
subject to risks and uncertainties, including those, if any, identified in the “Risk Factors” set forth in
this report or in our annual report on Form 10-K for the fiscal year ended March 31, 2024, filed with the Securities and Exchange Commission
(“SEC”) on June 24, 2024 and other documents that we subsequently file with the SEC that update, supplement
or supersede such information, which may cause actual results to differ materially from those expressed or implied in the forward-looking
statements. Forward-looking statements speak only as of the date when they are made. Except as required by federal securities law, we
do not undertake any obligation to update forward-looking statements to reflect events, circumstances, changes in expectations, or the
occurrence of unanticipated events after the date of those statements.
|
|
December 31, 2024, Form 10-Q |
PART
I – FINANCIAL INFORMATION
Item
1. Financial Statements
IGC
Pharma, Inc.
CONDENSED
CONSOLIDATED BALANCE SHEETS
(in
thousands, except share data)
(Unaudited)
| |
December 31, 2024 ($) | | |
March 31, 2024 ($) | |
ASSETS | |
| | |
| |
Current assets: | |
| | |
| |
Cash and cash equivalents | |
| 470 | | |
| 1,198 | |
Accounts receivable, net | |
| 49 | | |
| 39 | |
Inventory | |
| 1,433 | | |
| 1,540 | |
Asset held for sale | |
| 701 | | |
| 720 | |
Deposits and advances | |
| 398 | | |
| 208 | |
Total current assets | |
| 3,051 | | |
| 3,705 | |
| |
| | | |
| | |
Non-current assets: | |
| | | |
| | |
Intangible assets, net | |
| 1,869 | | |
| 1,616 | |
Property, plant, and equipment, net | |
| 3,348 | | |
| 3,695 | |
Claims and advances | |
| 681 | | |
| 688 | |
Operating lease asset | |
| 129 | | |
| 198 | |
Total non-current assets | |
| 6,027 | | |
| 6,197 | |
Total assets | |
| 9,078 | | |
| 9,902 | |
LIABILITIES AND STOCKHOLDERS’ EQUITY | |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Accounts payable | |
| 835 | | |
| 773 | |
Accrued liabilities and others | |
| 1,822 | | |
| 1,567 | |
Total current liabilities | |
| 2,657 | | |
| 2,340 | |
| |
| | | |
| | |
Non-current liabilities: | |
| | | |
| | |
Long-term loans | |
| 134 | | |
| 137 | |
Other liabilities | |
| 16 | | |
| 20 | |
Operating lease liability | |
| 12 | | |
| 84 | |
Total non-current liabilities | |
| 162 | | |
| 241 | |
Total liabilities | |
| 2,819 | | |
| 2,581 | |
| |
| | | |
| | |
Commitments and Contingencies – See Note 12 | |
| | | |
| | |
| |
| | | |
| | |
Stockholders’ equity: | |
| | | |
| | |
Preferred stock, $0.0001 par value: authorized 1,000,000 shares, no shares issued or outstanding as of December 31, 2024, and March 31, 2024. | |
| | | |
| | |
Common stock and additional paid-in capital, $0.0001 par value: 150,000,000 shares authorized; 78,203,218 and 66,691,195 shares issued and outstanding as of December 31, 2024, and March 31, 2024, respectively. | |
| 129,307 | | |
| 124,409 | |
Accumulated other comprehensive loss | |
| (3,459 | ) | |
| (3,423 | ) |
Accumulated deficit | |
| (119,589 | ) | |
| (113,665 | ) |
Total stockholders’ equity | |
| 6,259 | | |
| 7,321 | |
Total liabilities and stockholders’ equity | |
| 9,078 | | |
| 9,902 | |
The
accompanying notes should be read in connection with these Condensed Consolidated Financial Statements.
|
|
December 31, 2024, Form 10-Q |
IGC
Pharma, Inc.
CONDENSED
CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(in
thousands, except loss per share and share data)
(Unaudited)
| |
Three months ended December 31, | | |
Nine months ended December 31, | |
| |
2024 | | |
2023 | | |
2024 | | |
2023 | |
| |
($) | | |
($) | | |
($) | | |
($) | |
Revenue | |
| 257 | | |
| 204 | | |
| 941 | | |
| 1,050 | |
Cost of revenue | |
| (153 | ) | |
| (71 | ) | |
| (476 | ) | |
| (488 | ) |
Gross profit | |
| 104 | | |
| 133 | | |
| 465 | | |
| 562 | |
Selling, general and administrative expenses | |
| (1,130 | ) | |
| (2,228 | ) | |
| (3,841 | ) | |
| (5,272 | ) |
Research and development expenses | |
| (852 | ) | |
| (903 | ) | |
| (2,658 | ) | |
| (2,918 | ) |
Operating loss | |
| (1,878 | ) | |
| (2,998 | ) | |
| (6,034 | ) | |
| (7,628 | ) |
Impairment Loss on PPE | |
| - | | |
| (2,623 | ) | |
| - | | |
| (2,623 | ) |
Other income, net | |
| 49 | | |
| 32 | | |
| 110 | | |
| 136 | |
Loss before income taxes | |
| (1,829 | ) | |
| (5,589 | ) | |
| (5,924 | ) | |
| (10,115 | ) |
Income tax expense | |
| - | | |
| - | | |
| - | | |
| - | |
Net loss attributable to common stockholders | |
| (1,829 | ) | |
| (5,589 | ) | |
| (5,924 | ) | |
| (10,115 | ) |
Foreign currency translation adjustments | |
| (18 | ) | |
| 18 | | |
| (36 | ) | |
| (36 | ) |
Comprehensive loss | |
| (1,847 | ) | |
| (5,571 | ) | |
| (5,960 | ) | |
| (10,151 | ) |
| |
| | | |
| | | |
| | | |
| | |
Net loss per share attributable to common stockholders: | |
| | | |
| | | |
| | | |
| | |
Basic and diluted | |
$ | (0.02 | ) | |
| (0.09 | ) | |
| (0.08 | ) | |
| (0.18 | ) |
Weighted-average number of shares used in computing net loss per share amounts: | |
| 77,633,004 | | |
| 63,725,084 | | |
| 75,494,270 | | |
| 57,039,035 | |
The
accompanying notes should be read in connection with these Condensed Consolidated Financial Statements.
|
|
December 31, 2024, Form 10-Q |
IGC
Pharma, Inc.
CONDENSED
CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY
(in
thousands)
(Unaudited)
Three months ended December 31, 2023 | |
Number of Common Shares | | |
Common Stock and Additional Paid in Capital ($) | | |
Accumulated Deficit ($) | | |
Accumulated Other Comprehensive Loss ($) | | |
Total Stockholders’ Equity ($) | |
Balances as of September 30, 2023 | |
| 63,707 | | |
| 122,732 | | |
| (105,191 | ) | |
| (3,443 | ) | |
| 14,098 | |
Common stock-based compensation & expenses, net | |
| 27 | | |
| 526 | | |
| - | | |
| - | | |
| 526 | |
Share money received but not allotted | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
Issuance of common stock through offering (net of expenses) | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
Cancellation/forfeiture of shares | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
Net loss | |
| - | | |
| - | | |
| (5,589 | ) | |
| - | | |
| (5,589 | ) |
Foreign currency translation adjustments | |
| - | | |
| - | | |
| - | | |
| 18 | | |
| 18 | |
Balances as of December 31, 2023 | |
| 63,734 | | |
| 123,258 | | |
| (110,780 | ) | |
| (3,425 | ) | |
| 9,053 | |
| |
| | | |
| | | |
| | | |
| | | |
| | |
Three months ended December 31, 2024 | |
| | | |
| | | |
| | | |
| | | |
| | |
Balances as of September 30, 2024 | |
| 76,636 | | |
| 128,578 | | |
| (117,760 | ) | |
| (3,441 | ) | |
| 7,377 | |
Common stock-based compensation & expenses, net | |
| - | | |
| 384 | | |
| - | | |
| - | | |
| 384 | |
Share money received but not allotted | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
Issuance of common stock through offering (net of expenses) | |
| 1,567 | | |
| 345 | | |
| - | | |
| - | | |
| 345 | |
Cancellation/forfeiture of shares | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
Net loss | |
| - | | |
| - | | |
| (1,829 | ) | |
| - | | |
| (1,829 | ) |
Foreign currency translation adjustments | |
| - | | |
| - | | |
| - | | |
| (18 | ) | |
| (18 | ) |
Balances as of December 31, 2024 | |
| 78,203 | | |
| 129,307 | | |
| (119,589 | ) | |
| (3,459 | ) | |
| 6,259 | |
Nine months ended December 31, 2023 | |
Number of Common Shares | | |
Common Stock and Additional Paid in Capital ($) | | |
Accumulated Deficit ($) | | |
Accumulated Other Comprehensive Loss ($) | | |
Total Stockholders’ Equity ($) | |
Balances as of March 31, 2023 | |
| 53,077 | | |
| 118,965 | | |
| (100,665 | ) | |
| (3,389 | ) | |
| 14,911 | |
Common stock-based compensation & expenses, net | |
| 1,157 | | |
| 1,433 | | |
| - | | |
| - | | |
| 1,433 | |
Issuance of common stock through offering (net of expenses) | |
| 10,000 | | |
| 2,860 | | |
| - | | |
| - | | |
| 2,860 | |
Share money received but not allotted | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
Cancellation/forfeiture of shares | |
| (500 | ) | |
| - | | |
| - | | |
| - | | |
| - | |
Net loss | |
| - | | |
| - | | |
| (10,115 | ) | |
| - | | |
| (10,115 | ) |
Foreign currency translation adjustments | |
| - | | |
| - | | |
| - | | |
| (36 | ) | |
| (36 | ) |
Balances as of December 31, 2023 | |
| 63,734 | | |
| 123,258 | | |
| (110,780 | ) | |
| (3,425 | ) | |
| 9,053 | |
| |
| | | |
| | | |
| | | |
| | | |
| | |
Nine months ended December 31, 2024 | |
| | | |
| | | |
| | | |
| | | |
| | |
Balances as of March 31, 2024 | |
| 66,691 | | |
| 124,409 | | |
| (113,665 | ) | |
| (3,423 | ) | |
| 7,321 | |
Common stock-based compensation & expenses, net | |
| - | | |
| 1,251 | | |
| - | | |
| - | | |
| 1,251 | |
Share money received but not allotted | |
| - | | |
| 200 | | |
| - | | |
| - | | |
| 200 | |
Issuance of common stock through offering (net of expenses) | |
| 11,512 | | |
| 3,447 | | |
| - | | |
| - | | |
| 3,447 | |
Cancellation/forfeiture of shares | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
Net loss | |
| - | | |
| - | | |
| (5,924 | ) | |
| - | | |
| (5,924 | ) |
Foreign currency translation adjustments | |
| - | | |
| - | | |
| - | | |
| (36 | ) | |
| (36 | ) |
Balances as of December 31, 2024 | |
| 78,203 | | |
| 129,307 | | |
| (119,589 | ) | |
| (3,459 | ) | |
| 6,259 | |
The
accompanying notes should be read in connection with these Condensed Consolidated Financial Statements.
|
|
December 31, 2024, Form 10-Q |
IGC
Pharma, Inc.
CONDENSED
CONSOLIDATED STATEMENTS OF CASH FLOWS
(in
thousands)
(Unaudited)
| |
Nine months Ended December 31, | |
| |
2024
($) | | |
2023
($) | |
Cash flows from operating activities: | |
| | |
| |
Net loss | |
| (5,924 | ) | |
| (10,115 | ) |
Adjustment to reconcile net loss to net cash: | |
| | | |
| | |
Depreciation and amortization | |
| 464 | | |
| 473 | |
Common stock-based compensation and expenses, net | |
| 1,185 | | |
| 1,433 | |
Impairment of assets | |
| - | | |
| 3,358 | |
Profit on sale of assets, net | |
| (14 | ) | |
| (42 | ) |
| |
| | | |
| | |
Changes in: | |
| | | |
| | |
Accounts receivables, net | |
| (10 | ) | |
| 14 | |
Inventory | |
| 107 | | |
| (8 | ) |
Deposits and advances | |
| (190 | ) | |
| 169 | |
Claims and advances | |
| 7 | | |
| 4 | |
Accounts payable | |
| 62 | | |
| 117 | |
Accrued and other liabilities | |
| 251 | | |
| (83 | ) |
Operating lease asset | |
| 69 | | |
| 99 | |
Operating lease liability | |
| (72 | ) | |
| (92 | ) |
Net cash used in operating activities | |
| (4,065 | ) | |
| (4,673 | ) |
| |
| | | |
| | |
Cash flow from investing activities: | |
| | | |
| | |
Purchase of property, plant, and equipment | |
| (94 | ) | |
| (123 | ) |
Sale of property, plant, and equipment | |
| 16 | | |
| 42 | |
Investment in short term investments | |
| - | | |
| 154 | |
Acquisition and development of intangible assets | |
| (222 | ) | |
| (67 | ) |
Net cash (used in)/provided by investing activities | |
| (300 | ) | |
| 6 | |
| |
| | | |
| | |
Cash flows from financing activities: | |
| | | |
| | |
Net proceeds from the issuance of common stock | |
| 3,649 | | |
| 2,860 | |
Repayment of long-term loan | |
| (3 | ) | |
| (3 | ) |
Net cash provided by financing activities | |
| 3,646 | | |
| 2,857 | |
| |
| | | |
| | |
Effects of exchange rate changes on cash and cash equivalents | |
| (9 | ) | |
| (8 | ) |
Net (decrease) in cash and cash equivalents | |
| (728 | ) | |
| (1,818 | ) |
Cash and cash equivalents at the beginning of the period | |
| 1,198 | | |
| 3,196 | |
Cash and cash equivalents at the end of the period | |
| 470 | | |
| 1,378 | |
| |
| | | |
| | |
Supplementary information: | |
| | | |
| | |
Non-cash items: | |
| | | |
| | |
Common stock issued/granted for stock-based compensation, including patent acquisition. | |
| 1,250 | | |
| 1,433 | |
The
accompanying notes should be read in connection with these Condensed Consolidated Financial Statements.
|
|
December 31, 2024, Form 10-Q |
IGC
Pharma, Inc.
NOTES
TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS
THREE
MONTHS AND NINE MONTHS ENDED DECEMBER 31, 2024
(in
thousands, except for share data and loss per share, unaudited)
Unless
the context requires otherwise, all references in this report to “IGC,” “IGC Pharma,” “the
Company,” “we,” “our” and/or “us” refer to IGC Pharma, Inc.,
together with our subsidiaries and beneficially owned subsidiary. Our public filings with the Securities and Exchange Commission, the
“SEC,” are available on www.sec.gov. The information contained on our various websites, including www.igcinc.us,
is not incorporated by reference in this report, and you should not consider such information to be a part of this report. We exclude
our investments and minority non-controlling interests, and any information provided by them is not incorporated by reference in this
report, and you should not consider such information to be a part of this report.
NOTE
1 – BUSINESS DESCRIPTION
Overview
IGC
Pharma, a clinical-stage company developing treatments for Alzheimer’s disease, is committed to transforming patient care by striving
to offer faster-acting and more effective solutions. Our leading drug candidate, IGC-AD1, embodies this vision by tackling a critical
challenge – managing agitation in Alzheimer’s dementia. Early results from our Phase 2 trial are promising: IGC-AD1 effectively
reduced agitation in patients compared to a placebo, and crucially, it did so faster than traditional medications. While existing anti-psychotics
can take as long as 6 to 12 weeks to show effects, IGC-AD1 has the potential to act within 2 weeks. This significantly faster onset of
action could significantly improve patient care and represents a potential breakthrough in managing Alzheimer’s-related agitation,
although there can be no assurance thereof.
We
currently have five platforms, each with a core molecule that can be modified. For example, the TGR family consists of many molecules,
such as TGR-60, TGR-61, and TGR-63. TGR-63 targets plaques in Alzheimer’s. Similarly, the IGC-C and IGC-M platforms consist of
many molecules. The Alzheimer’s targeting molecule from each of our platforms is set forth below, the effects of which are subject
to clinical trial and investigation:
| ● | IGC-AD1:
Our lead investigational drug tackles agitation, a major burden for patients and caregivers. By addressing neuroinflammation, it
has the potential to offer a faster-acting solution compared to traditional medications. |
| ● | TGR-63:
Through pre-clinical studies, TGR-63 has demonstrated its potential to disrupt the progression of Alzheimer’s by targeting
Aβ plaques, a key disease hallmark. |
| ● | IGC-1C:
At the preclinical stage, IGC-1C represents a potential breakthrough by targeting tau protein and neurofibrillary tangles, aiming
to modify the disease course. |
| ● | IGC-M3:
Also in preclinical development, IGC-M3 focuses on early intervention by inhibiting Aβ plaque formation, potentially slowing
cognitive decline. |
| ● | LMP:
In preclinical development, LMP is designed to target multiple hallmarks of Alzheimer’s disease, including Aβ plaques
and neurofibrillary tangles, for a comprehensive therapeutic effect. |
A
goal of IGC’s, in addition to advancing our drugs through the clinical trial, is to also drive near to mid-term revenue growth.
We have made considerable investments to date across our platform in our consumer products division, artificial intelligence (“AI”),
and our internal Customer Relationship Management (“CRM”). It is our view that there is an opportunity to drive revenue growth
in these parts of our business without significant future capital investment.
We
are also developing AI models for predicting early Alzheimer’s detection biomarkers, optimizing clinical trials, and to help us
explore new disease applications for different molecules. For example, our AI models are being developed to predict the probability that
our molecules can work on other receptors, such as GLP1 (neurological disorders, weight loss), CB1 (neuropsychiatric conditions), among
others. Additionally, our 30 patent filings, including for IGC-AD1, demonstrate our commitment to innovation and protecting our intellectual
property. Collectively, these core assets and initiatives underscore our commitment to advancing the field of pharmaceuticals, delivering
groundbreaking treatments, and creating lasting value for our investors. We remain steadfast in our pursuit of excellence and our mission
to improve the lives of those affected by Alzheimer’s and related conditions.
|
|
December 31, 2024, Form 10-Q |
Update:
Phase
2 Clinical Trial
IGC
Pharma launched a Phase 2 trial with a protocol titled “A Phase 2, Multi-Center, Double-Blind, Randomized, Placebo-controlled,
trial of the safety and efficacy of IGC-AD1 on agitation in participants with dementia due to Alzheimer’s disease” (clinicaltrials.gov,
Identifier: CT05543681). The study is powered to include 146 Alzheimer’s patients; as a superiority trial with parallel groups;
half of the participants will receive a placebo, and the other half will receive IGC-AD1.
The
primary and secondary endpoints are the mean change in agitation scores from baseline, compared to placebo, as assessed by the Cohen-Mansfield
Agitation Inventory (“CMAI”) in Alzheimer’s patients after 6 weeks of treatment and the mean change in CMAI scores
after 2 weeks of treatment, respectively. Agitation is rated at the trial site, at baseline, week 2, and week 6, by a trained practitioner
using the CMAI, a scale designed and widely used to measure agitation in Alzheimer’s dementia (“AAD”) in clinical trials.
The IGC-AD1 Phase 2 is an ongoing clinical trial that continues to enroll. IGC-AD1 is an oral liquid formulation administered twice daily
(“bid”) for six weeks with no placebo run-in and titration to full dose over two days. To date over 1,000 oral doses have
been administered, with no dose-limiting adverse events observed, highlighting the safety profile of IGC-AD1. The investigational product
potentially targets different pathways implicated in agitation in Alzheimer’s dementia (“AAD”), including CB1 receptor
dysfunction, neuroinflammation, and neurotransmitter imbalance.
AI
/ Machine Learning (“ML”)
In
our pursuit of innovation, we leverage AI and ML. AI refers to the development of intelligent systems that can learn and act autonomously.
ML is a branch of AI that allows computers to learn from data without the need for explicit programming. This technology plays a role
in our efforts and could allow companies our size to do what previously was the domain of much larger pharmaceutical companies. For instance,
we are utilizing ML by training transformers, a powerful neural network architecture, to analyze vast datasets from our Phase 1 and unblinded
Phase 2 interim clinical trial to identify patterns and optimize the clinical trial protocol for a potential Phase 3 trial. The AI model,
for example, can tell us if a particular neuropsychiatric scale that we used in Phase 1 and Phase 2 added valuable information to the
trial, and if it did not, we could remove that scale from a future Phase 3 trial, thus saving money and time in the overall trial management.
In the long term, with more data, the trained AI model could allow us to consider incoming patient signatures, such as scans, symptoms,
patient history, among others and predict outcomes for our drug, including adverse effects, thus personalizing the delivery of IGC-AD1,
of which there can be no assurance.
Additionally,
we are developing AI models that help us explore potential applications of molecules from our platforms beyond their initial Alzheimer’s
targets; we know that TGR-63 and IGC-M3 target plaques in Alzheimer’s, however, AI models could help us consider applications of
TGR-60, TGR-61, IGC-M1, IGC-M2, and many others. For example, we are investigating whether our molecules might interact with other receptors,
like GLP-1. GLP-1 is a receptor linked to regulating blood sugar and is increasingly being studied for its potential role in neurological
disorders, in addition to its established role in weight management. A successful link between our molecules and other targets potentially
expands our opportunities, as some of these other markets, such as the weight loss market, are considerably larger than the Alzheimer’s
market. These applications could potentially lead, if proven in future clinical trials, to new treatment avenues and broader market reach
for our molecules. This analysis also potentially allows us to prioritize work on our molecules and optimize our resources.
Business
Organization
As
of December 31, 2024, the Company had the following operating subsidiaries: IGCare LLC, HH Processors, LLC, IGC Pharma, LLC, IGC Pharma
IP, LLC, SAN Holdings, LLC, Sunday Seltzer, LLC, Hamsa Biopharma India Pvt. Ltd., Techni Bharathi Private Limited (TBL), and Colombia-based
beneficially-owned subsidiary IGC Pharma SAS. The Company’s fiscal year is the 52- or 53-week period that ends on March 31. IGC
has two business segments: Life Sciences Segment and Infrastructure Segment. For more information on the business segments, please refer
to Item 7, “Management’s Discussion and Analysis of Financial Condition and Results of Operations”. The Company’s
principal office is in Maryland, established in 2005. Additionally, the Company has offices in Washington state, Colombia, South America,
and India. The Company’s filings are available on www.sec.gov.
|
|
December 31, 2024, Form 10-Q |
NOTE
2 – SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Basis
of presentation
The
accompanying condensed consolidated balance sheet as of December 31, 2024, and March 31, 2024, condensed consolidated statements of operations
for the three months and nine months ended December 31, 2024, and 2023, and condensed consolidated statements of cash flows for the nine
months ended December 31, 2024, and 2023, are unaudited. The consolidated balance sheet as of March 31, 2024, has been derived from audited
financial statements, and the accompanying as of December 31, 2024 unaudited condensed consolidated financial statements (“interim
statements”) of the Company have been prepared in accordance with accounting principles generally accepted in the U.S. (“U.S.
GAAP”) as determined by the Financial Accounting Standards Board (the “FASB”) within its Accounting Standards Codification
(“ASC”) and under the rules and regulations of the SEC.
Accordingly,
they do not include all the information and footnotes required by U.S. GAAP for complete financial statements. In the opinion of management,
all adjustments and disclosures necessary for a fair presentation of these interim statements have been included. The results reported
in these interim statements are not necessarily indicative of the results that may be reported for the entire year. These interim statements
should be read in conjunction with the Company’s audited consolidated financial statements for the fiscal year ended March 31,
2024 (“Fiscal 2024”) contained in the Company’s Form 10-K for Fiscal 2024, filed with the SEC on June 24, 2024, specifically
in Note 2 to the consolidated financial statements.
Principles
of consolidation
The
interim statements include the consolidated accounts of the Company and its subsidiaries. Intercompany accounts and transactions have
been eliminated. In the opinion of the Company’s management, the interim statements reflect all adjustments, which are normal and
recurring in nature, necessary for fair financial statement presentation. Transactions between the Company and its subsidiaries are eliminated
in the consolidated financial statements.
Presentation
and functional currencies
The
Company operates in the U.S., Colombia, and India and a portion of the Company’s financials are denominated in the Indian Rupee
(“INR”), or the Colombian Peso (“COP”). As a result, changes in the relative values of the U.S. Dollar (“USD”),
the INR, or the COP affect our financial statements.
The
accompanying financial statements are reported in USD. INR and COP are the functional currencies for certain subsidiaries of the Company.
The translation of the functional currencies into USD is performed for assets and liabilities using the exchange rates in effect at the
balance sheet date and for revenues and expenses using average exchange rates prevailing during the reporting periods. Adjustments resulting
from the translation of functional currency financial statements to reporting currency are accumulated and reported as other comprehensive
(loss), a separate component of shareholders’ equity. Transactions in currencies other than the functional currency during the
year are converted into the functional currency at the applicable rates of exchange prevailing when the transactions occurred. Transaction
gains and losses are recognized in the consolidated statements of operations.
Going
Concern
The
Company assesses and determines its ability to continue as a going concern in accordance with the provisions of ASC Subtopic 205-40,
“Presentation of Financial Statements—Going Concern”, which requires the Company to evaluate whether
there are conditions or events that raise substantial doubt about its ability to continue as a going concern.
The
Company is currently in a clinical trial stage and, thus, has not yet achieved profitability. The Company expects to continue to incur
significant operating and net losses and negative cash flows from operations in the near future.
The
Company estimates that its current cash and cash equivalents balance with the working capital and investments with available overdraft
facility of 12 million from O-Bank are sufficient to support operations beyond the twelve months following the date these consolidated
financial statements and footnotes were issued. These estimates are based on assumptions that may prove to be wrong, and the Company
could use its available capital resources sooner than it currently expects.
|
|
December 31, 2024, Form 10-Q |
Accounts
receivable
We
make estimates of the collectability of our accounts receivable by analyzing historical payment patterns, customer concentrations, customer
creditworthiness, and current economic trends. If the financial condition of a customer deteriorates, additional allowances may be required.
We had $49 thousand of accounts receivable, net of provision for the doubtful debt of $20 thousand as of December 31, 2024, as compared
to $39 thousand of accounts receivable, net of provision for the doubtful debt of $24 thousand as of March 31, 2024.
Loss
per share
The
computation of basic loss per share for the nine months ended December 31, 2024, excludes potentially dilutive securities of approximately
12 million shares, which includes unvested or unexercised share options, unvested shares, such as restricted shares and restricted share
units, granted to employees, non-employees, and advisors, and shares from the conversion of outstanding units, if any because their inclusion
would be anti-dilutive.
The
weighted average number of shares outstanding for the nine months ended December 31, 2024, and 2023, used for the computation of basic
earnings per share (“EPS”) is 75,494,270 and 57,039,035, respectively, as compared to 77,633,004 and 63,725,084 for the three
months ended December 31, 2024, and 2023, respectively. Due to the loss incurred by the Company during the nine months ended December
31, 2024, and 2023, all the potential equity shares are anti-dilutive, and accordingly, the fully diluted EPS is equal to the basic EPS.
Cybersecurity
We
have a cybersecurity policy in place and have taken cybersecurity measures to safeguard against hackers, however, there can be no assurance
thereof. During the nine months ended December 31, 2024, there were no impactful breaches in cybersecurity.
Revenue
Recognition
The
Company recognizes revenue under ASC 606, Revenue from Contracts with Customers (ASC 606). The core principle of this standard
is that a company should recognize revenue to depict the transfer of promised goods or services to customers in an amount that reflects
the consideration to which the Company expects to be entitled in exchange for those goods or services.
ASC
606 prescribes a 5-step process to achieve its core principle. The Company recognizes revenue from trading, rental, or product sales
as follows:
| I. | Identify
the contract with the customer. |
| II. | Identify
the contractual performance obligations. |
| III. | Determine
the amount of consideration/price for the transaction. |
| IV. | Allocate
the determined amount of consideration/price to the performance obligations. |
| V. | Recognize
revenue when or as the performing party satisfies performance obligations. |
The
consideration/price for the transaction (performance obligation(s)) is determined as per the agreement or invoice (contract) for the
services and products in the Infrastructure and Life Sciences segment.
Revenue
in the Infrastructure segment is recognized for the renting business when the equipment is rented, and the terms of the agreement have
been fulfilled during the period. Revenue from the execution of infrastructure contracts is recognized based on the output method as
and when part of the performance obligation has been completed, and approval from the contracting agency has been obtained after survey
of the performance completion as of that date. In the Life Sciences segment, the revenue from the wellness and lifestyle business is
recognized once goods have been sold to the customer and the performance obligation has been completed. In retail sales, we offer consumer
products through our online stores. Revenue is recognized when control of the goods is transferred to the customer. This generally occurs
upon our delivery to a third-party carrier or to the customer directly. Revenue from white label services is recognized when the performance
obligation has been completed, and output material has been transferred to the customer.
|
|
December 31, 2024, Form 10-Q |
Net
sales disaggregated by significant products and services for the three months and nine months ended December 31, 2024, and 2023 are as
follows:
| |
(in
thousands)
Three months
ended
December 31,
2024
($) | | |
(in
thousands)
Three months
ended
December 31,
2023
($) | | |
(in
thousands)
Nine months
ended
December 31,
2024
($) | | |
(in
thousands)
Nine months
ended
December 31,
2023
($) | |
Infrastructure segment (1) | |
| - | | |
| - | | |
| - | | |
| 161 | |
| |
| | | |
| | | |
| | | |
| | |
Life Sciences segment | |
| | | |
| | | |
| | | |
| | |
Wellness and lifestyle (2) | |
| 34 | | |
| 47 | | |
| 101 | | |
| 165 | |
White labeling services (3) | |
| 223 | | |
| 157 | | |
| 841 | | |
| 724 | |
Total | |
| 257 | | |
| 204 | | |
| 941 | | |
| 1,050 | |
Recently
issued accounting pronouncements
Changes
to U.S. GAAP are established by the FASB in the form of accounting standards updates (“ASUs”) to the FASB’s ASC. The
Company considers the applicability and impact of all ASUs. Newly issued ASUs not listed are expected to have no impact on the Company’s
consolidated financial position and results of operations, because either the ASU is not applicable, or the impact is expected to be
immaterial.
NOTE
3 – INVENTORY
| |
(in thousands) | |
| |
As
of December 31,
2024
($) | | |
As
of
March 31,
2024
($) | |
Raw materials | |
| 1,069 | | |
| 1,099 | |
Work-in-Progress | |
| - | | |
| - | |
Finished goods | |
| 364 | | |
| 441 | |
Total | |
| 1,433 | | |
| 1,540 | |
Abnormal
amounts of idle facility expense, freight, handling costs, scrap, and wasted material (spoilage) are expensed in the period they are
incurred. During the nine months ended December 31, 2024, and 2023, the Company wrote off approximately $50 thousand and $746 thousand primarily
related to obsolete and expired stock.
We
capitalize inventory costs related to our investigational drug, provided that management determines there is a potential alternative
use for the inventory in future research and development projects or other purposes. As of December 31, 2024, and March 31, 2024, our
consolidated balance sheet reported approximately $392 thousand clinical trial-related inventory, respectively.
NOTE
4 – DEPOSITS AND ADVANCES
| |
(in thousands) | |
| |
As
of
December 31,
2024
($) | | |
As
of
March 31,
2024
($) | |
Advances to suppliers and consultants | |
| 51 | | |
| 41 | |
Other receivables and deposits | |
| 43 | | |
| 52 | |
Prepaid expenses and other current assets | |
| 304 | | |
| 115 | |
Total | |
| 398 | | |
| 208 | |
|
|
December 31, 2024, Form 10-Q |
The
Advances to suppliers and consultants primarily relate to advances to vendors. Prepaid expenses and other current assets include approximately
$50 thousand statutory advances as of December 31, 2024, and approximately $39 thousand as of March 31, 2024, respectively. In addition,
during the nine months ended December 31, 2024, prepaid expenses and other current assets include approximately $187 thousand related
to the asset held for sale.
NOTE
5 – INTANGIBLE ASSETS
| |
(in thousands) | |
| |
As
of
December 31,
2024
($) | | |
As
of
March 31,
2024
($) | |
Amortized intangible assets | |
| | |
| |
Patents | |
| 748 | | |
| 836 | |
Other intangibles | |
| 34 | | |
| 34 | |
Accumulated amortization | |
| (211 | ) | |
| (181 | ) |
Total amortized intangible assets | |
| 571 | | |
| 689 | |
| |
| | | |
| | |
Other intangible assets | |
| | | |
| | |
Patents | |
| 556 | | |
| 521 | |
Software development cost | |
| 742 | | |
| 406 | |
Total unamortized intangible assets | |
| 1,298 | | |
| 927 | |
Total intangible assets | |
| 1,869 | | |
| 1,616 | |
The
value of intangible assets includes the cost of acquiring patent rights, supporting data, and the expense associated with filing various
patent applications in different countries along with granted patents. It also includes acquisition costs related to domains and licenses.
The
amortization of patent and patent rights with finite life is up to 20 years, commencing from the date of grant or acquisition. The amortization
expense in the three months ended December 31, 2024, and 2023, amounted to approximately $17 thousand and $20 thousand, respectively,
whereas the amortization expense in the nine months ended December 31, 2024, and 2023 amounted to approximately $54 thousand and $55
thousand, respectively.
The
Company regularly reviews its intangible assets to determine if any intangible asset is other-than-temporarily impaired, which would
require the Company to record an impairment charge in the period and concluded that, as of December 31, 2024, there was no impairment.
Estimated annual amortization expense | |
(in thousands) ($) | |
For the year ended 2026 | |
| 59 | |
For the year ended 2027 | |
| 65 | |
For the year ended 2028 | |
| 72 | |
For the year ended 2029 | |
| 79 | |
For the year ended 2030 | |
| 87 | |
NOTE
6 – PROPERTY, PLANT, AND EQUIPMENT
| |
(in thousands, except useful life) | |
| |
Useful Life (years) | | |
As
of
December 31,
2024 ($) | | |
As of March 31,
2024 ($) | |
Buildings and facilities | |
25 | | |
| 2,331 | | |
| 2,303 | |
Plant and machinery | |
5-20 | | |
| 3,107 | | |
| 3,334 | |
Computer equipment | |
3 | | |
| 179 | | |
| 166 | |
Office equipment | |
3-5 | | |
| 132 | | |
| 140 | |
Furniture and fixtures | |
5 | | |
| 99 | | |
| 93 | |
Vehicles | |
5 | | |
| 101 | | |
| 101 | |
Total gross value | |
| | |
| 5,949 | | |
| 6,137 | |
Less: Accumulated depreciation | |
| | |
| (2,601 | ) | |
| (2,442 | ) |
Total property, plant, and equipment, net | |
| | |
| 3,348 | | |
| 3,695 | |
|
|
December 31, 2024, Form 10-Q |
The
depreciation expense in the three months ended December 31, 2024, and 2023 amounted to approximately $144 thousand and $140 thousand,
respectively. The depreciation expense in the nine months ended December 31, 2024, and 2023 amounted to approximately $431 thousand and
$417 thousand, respectively. For more information, please refer to Note 16 – “Segment Information” for the non-current
assets other than financial instruments held in the country of domicile and foreign countries.
Asset
Held For Sale
During
Fiscal 2024, the Company focused on liquidating all non-operating assets to reduce costs and generate cash. As a result, the Company
impaired the land situated in Nagpur, India, by approximately $3.3 million to $720 thousand from $4.1 million to bring it closer to the
fair market value. The Company believes it can sell the above-said non-operating land as it is without any improvement. Selling this
land will give immediate cash, which the Company can use in its operating segments.
During
the nine months ended December 31, 2024, the Company entered into an agreement with the buyer to sell the said land for a net realizable
value of approximately $701 thousand. The agreement is subject to the final registration and execution. The Company received a net of
approximately $344 thousand as a deposit. The Company holds the ownership and possession of the said land.
NOTE
7 – LEFT BLANK INTENTIONALLY
NOTE
8 – CLAIMS AND ADVANCES
| |
(in thousands) | |
| |
As of December 31,
2024 ($) | | |
As of March 31,
2024 ($) | |
Claims receivable (1) | |
| 679 | | |
| 686 | |
Non-current deposits | |
| 2 | | |
| 2 | |
Total | |
| 681 | | |
| 688 | |
NOTE
9 – LEFT BLANK INTENTIONALLY
NOTE
10 – ACCRUED AND OTHER LIABILITIES
| |
(in thousands) | |
| |
As of December 31,
2024 ($) | | |
As of March 31,
2024 ($) | |
Compensation and other contributions | |
| 864 | | |
| 816 | |
Provision for expenses | |
| 117 | | |
| 208 | |
Short-term lease liabilities | |
| 124 | | |
| 124 | |
Other current liabilities | |
| 717 | | |
| 419 | |
Total | |
| 1,822 | | |
| 1,567 | |
|
|
December 31, 2024, Form 10-Q |
Compensation
and other contribution-related liabilities consist of accrued salaries to employees. In addition, provision for expenses includes provision
for legal, professional, and marketing expenses. Other current liabilities also include statutory payables of approximately $14 thousand
and $25 thousand as of December 31, 2024, and March 31, 2024, respectively, and approximately $3 thousand of short-term loans as of December
31, 2024, and March 31, 2024, respectively. In addition, during the nine months ended, December 31, 2024, the Company received approximately
$550 thousand related to asset held for sale. Please refer to Note 6 – “Property, plant and, equipment”, for more information.
NOTE
11 – LOANS AND OTHER LIABILITIES
Loan
as of December 31, 2024:
On
June 11, 2020, the Company received an Economic Injury Disaster Loan (“EIDL”) for approximately $150 thousand at an annual
interest rate of 3.75%. The Company must pay principal and interest payments of $731 every month beginning June 5, 2021. The SBA will
apply each installment payment first to pay interest accrued to the day the SBA receives the payment and will then apply any remaining
balance to reduce the principal. All remaining principal and accrued interest is due and payable 30 years from the date of the loan.
For the nine months ended December 31, 2024, the interest expense and principal payment for the EIDL were approximately $4 thousand and
$3 thousand, respectively. For the nine months ended December 31, 2023, the interest expense and principal payment for the EIDL were
approximately $4 thousand and $2 thousand, respectively. As of December 31, 2024, approximately $134 thousand of the loan is classified
as Long-term loans and approximately $3 thousand as Short-term loans.
On
June 30, 2023, (the “Effective Date”), the Company entered into a Master Loan and Security Agreement along with the General
Banking Facility Letter (collectively called the “Credit Agreement”) with O-Bank Co., Ltd., a banking corporation incorporated
under the laws of Taiwan, as administrative agent and lender (the “Lender’) pursuant to which the Borrower may borrow up
to USD$12,000,000.00 only or the equivalent thereof in other major currencies (the “Credit Facility”). The Credit Facility
under the Credit Agreement contained a maturity date on the first anniversary of the Effective Date. Borrowings under the Loan Agreement
will bear interest, calculated according to the interest rate mentioned in the Certificate of Deposit, as the case may be, plus an applicable
margin of 1%, and the Borrower shall bear the tax. Interest is due and payable in full by the Borrower on the last business day of each
interest period. On July 29, 2024, the Company entered into an amendment to extend the Credit Agreement with the Lender effective July
8, 2024. The amendment extended the term of the Loan Agreement, which was set to expire, under the same terms and conditions as previously
disclosed on the Company’s Current Report on Form 8-K filed with the Securities Exchange Commission on July 7, 2023, with the exception
of a reduction in the facility fees from $120,000 to $84,000. All other material terms of the Credit Agreement remain unchanged.
Other
Liability:
| |
(in thousands) | |
| |
As of | |
| |
December
31,
2024
($) | | |
March
31,
2024
($) | |
Statutory reserve | |
| 16 | | |
| 20 | |
Total | |
| 16 | | |
| 20 | |
The
statutory reserve is a gratuity reserve for employees in our subsidiaries in India.
NOTE
12 – COMMITMENTS AND CONTINGENCIES
The
Company may be involved in legal proceedings, claims, and assessments arising in the ordinary course of business. Such matters are subject
to many uncertainties, and outcomes are not predictable with assurance. There are no such matters that are deemed material to the condensed
consolidated financial statements as of December 31, 2024, except as disclosed in the legal proceedings section below.
|
|
December 31, 2024, Form 10-Q |
In
the U.S., we provide health insurance, life insurance, and a 401(k) plan wherein the Company matches up to 6% of the employee’s
pre-tax contribution up to a maximum annual amount determined by the IRS. In accordance with applicable laws of foreign countries, the
Company provides for gratuity, a defined benefit retirement plan (“Gratuity Plan”) covering certain categories of employees.
The Gratuity Plan provides a lump sum payment to vested employees, at retirement or termination of employment, an amount based on the
respective employee’s last drawn salary and the years of employment with the Company. In addition, employees receive benefits from
a provident fund, a defined contribution plan. The employee and employer each make monthly contributions to the plan as required by the
law. The contribution is made to the Foreign Government’s funds.
NOTE
13 – SECURITIES
As
of December 31, 2024, the Company was authorized to issue up to 150,000,000 shares of common stock, par value $0.0001 per share, and
78,203,218 shares of common stock were issued and outstanding. The Company is also authorized to issue up to 1,000,000 shares of preferred
stock, par value $0.0001 per share, and no preferred shares were issued and outstanding as of December 31, 2024.
Our
common stock is listed on the NYSE American (ticker symbol: IGC). This security also trades on the Frankfurt, Stuttgart, and Berlin stock
exchanges (ticker symbol: IGS1). The Company also has 91,472 units outstanding that can be separated into common stock. Ten units may
be separated into one share of common stock. The unit holders are requested to contact the Company or our transfer agent, Continental
Stock Transfer and Trust, to separate their units into common stock.
On
March 22, 2024, the Company entered into a Share Purchase Agreement (the “March 2024 SPA”) with Bradbury Strategic Investment
Fund A, resulting in approximately $3 million in gross proceeds. During the quarter ended June 30, 2024, the Company issued approximately
8.8 million shares of unregistered common stock at a price of $0.34 per share. Shares are intended to be exempt from registration under
the Securities Act of 1933, as amended (the “Securities Act”), by virtue of the provisions of Section 4(a)(2) of the Securities
Act and Regulation D and/or Regulation S adopted thereunder. During fiscal 2024, the Company had received $500 thousand of the total
$3 million due under the March 2024 SPA, while the remaining $2.5 million was received in April 2024.
On
September 25, 2024, the Company entered into the 2024 Share Purchase Agreement (the “September 2024 SPA”) with Moran Global
Strategies, Inc., a Virginia corporation (“MGS”), which is owned by James Moran, a director of IGC, relating to the sale
and issuance by our company to the investors of an aggregate of 588,235 shares of our common stock, for a total purchase price of $200,000
or $0.34 per share, subject to the terms and conditions set forth in the September 2024 SPA. The investment is subject to customary closing
conditions, including NYSE approval. As per the September 2024 SPA, the investor received piggyback registration rights subject to certain
restrictions. During the nine months ended December 31, 2024, the Company received the purchase price, and the issuance of common stock
are under process.
NOTE
14 – STOCK-BASED COMPENSATION
As
of December 31, 2024, under both the Company’s previous 2008 and current 2018 Omnibus Incentive Plans approximately 9.1 million
shares of common stock have been issued to employees, non-employees, and advisors. In addition, 7.5 million restricted share units (“RSUs”)
fair valued at $4.3 million with a weighted average value of $0.61 per share, have been granted but not yet issued from different Incentive
Plans and Grants. This includes 4.9 million RSUs granted to employees and directors, which consists of a vesting schedule based entirely
on the attainment of either operational milestones (performance conditions) or market conditions, assuming continued employment either
as an employee, or director with the Company. The performance-based RSUs are accounted for upon certification by the management, confirming
the probability of achievement of milestones. As of December 31, 2024, the management confirmed that five milestones had been achieved,
and the rest were probable to be achieved by March 31, 2028.
Additionally,
stock options to purchase 3.7 million shares of common stock fair valued at $928 thousand with a weighted average of $0.25 per share,
which have been granted but are to be issued over a vesting period between Fiscal 2025 and Fiscal 2027.
|
|
December 31, 2024, Form 10-Q |
The
stock options are valued using a Black-Scholes Pricing Model, and Market-based RSUs are valued based on a lattice model, with the following
assumptions:
| | Granted in Fiscal 2025 | | | Granted in Fiscal 2024 | |
Expected life of options | | 5 years | | | 5 years | |
Vested options | | | 100 | % | | | 100 | % |
Risk-free interest rate | | | 4.49 | % | | | 5.24 | % |
Expected volatility | | | 174 | % | | | 175 | % |
Expected dividend yield | | Nil | | | Nil | |
The
expense associated with share-based payments to employees, directors, advisors, and contractors is allocated over the vesting or service
period and recognized in the Selling, general, and administrative expenses (including research and development). For the nine months
ended December 31, 2024, the Company’s share-based expense and option-based expense shown in Selling, general, and administrative
expenses (including research and development) were $815 thousand and $435 thousand, respectively, and for the nine months ended December
31, 2023, the Company’s share-based expense and option-based expense was $1.4 million and $9 thousand, respectively.
Non-vested shares | |
Shares (in thousands) (#) | | |
Weighted
average grant date fair
value ($) | |
Non-vested shares as of March 31, 2024 | |
| 7,452 | | |
| 0.61 | |
Granted | |
| - | | |
| - | |
Vested | |
| (150 | ) | |
| 0.43 | |
Cancelled/forfeited | |
| (30 | ) | |
| 0.30 | |
Non-vested shares as of December 31, 2024 | |
| 7,272 | | |
| 0.61 | |
Options | |
Shares (in thousands) (#) | | |
Weighted
average grant date fair
value ($) | | |
Weighted
average exercise price ($) | |
Options outstanding as of March 31, 2024 | |
| 3,710 | | |
| 0.25 | | |
| 0.29 | |
Granted | |
| - | | |
| - | | |
| - | |
Exercised | |
| - | | |
| - | | |
| - | |
Cancelled/forfeited | |
| - | | |
| - | | |
| - | |
Options outstanding as of December 31, 2024 | |
| 3,710 | | |
| 0.25 | | |
| 0.29 | |
As
of December 31, 2024, there was a combined unrecognized expense of $1.98 million related to non-vested shares and share options that
the Company expects to be recognized over a life of up to 4 years.
NOTE
15 – FAIR VALUE OF FINANCIAL INSTRUMENTS
As
of December 31, 2024, the Company’s investments may consist of money market funds, debt and equity funds, and other marketable
securities, among others, which have been classified as Level 1 of the fair value hierarchy because they have been valued using quoted
prices in active markets. The Company’s cash and cash equivalents have also been classified as Level 1 on the same principle. Financial
instruments are classified as current if they are expected to be liquidated within the next twelve months. The Certificates of Deposit
are classified as Level 2 as they do not have regular market pricing, but their fair value can be determined based on other data values
or market prices. The Company’s remaining investments have been classified as Level 3 instruments as there is little or no market
data. Level 3 investments are valued using the cost method.
|
|
December 31, 2024, Form 10-Q |
The
following table presents information about the Company’s assets that are measured at fair value on a recurring basis as of December
31, 2024, and March 31, 2024, and indicates the fair value hierarchy of the valuation techniques the Company used to determine such fair
value:
(in
thousands)
As
of December 31, 2024
Particular | |
Adjusted Cost ($) | | |
Gain ($) | | |
Loss ($) | | |
Fair Value ($) | | |
Cash & Cash Equivalents ($) | | |
Short Term Investments ($) | |
Level 1 | |
| | |
| | |
| | |
| | |
| | |
| |
Cash | |
| 395 | | |
| - | | |
| - | | |
| 395 | | |
| 395 | | |
| - | |
Money Market Fund | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
Debt Funds | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
Mutual Fund | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
Level 2 | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Certificates of Deposit | |
| 75 | | |
| - | | |
| - | | |
| 75 | | |
| 75 | | |
| - | |
Level 3 | |
| | | |
| | | |
| | | |
| | | |
| | | |
| - | |
TOTAL | |
| 470 | | |
| - | | |
| - | | |
| 470 | | |
| 470 | | |
| - | |
As
of March 31, 2024
Particular | |
Adjusted Cost ($) | | |
Gain ($) | | |
Loss ($) | | |
Fair Value ($) | | |
Cash & Cash Equivalents ($) | | |
Short Term Investments ($) | |
Level 1 | |
| | |
| | |
| | |
| | |
| | |
| |
Cash | |
| 912 | | |
| - | | |
| - | | |
| 912 | | |
| 912 | | |
| - | |
Money Market Fund | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
Debt Funds | |
| 13 | | |
| - | | |
| - | | |
| 13 | | |
| 13 | | |
| - | |
Mutual Fund | |
| 123 | | |
| - | | |
| - | | |
| 123 | | |
| 123 | | |
| - | |
Level 2 | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Certificates of Deposit | |
| 150 | | |
| - | | |
| - | | |
| 150 | | |
| 150 | | |
| - | |
Level 3 | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
TOTAL | |
| 1,198 | | |
| - | | |
| - | | |
| 1,198 | | |
| 1,198 | | |
| - | |
NOTE
16 – SEGMENT INFORMATION
FASB
ASC 280, “Segment Reporting,” establishes standards for reporting information about reportable segments. Operating
segments are defined as components of an enterprise about which separate financial information is available that is evaluated regularly
by the chief operating decision maker, or decision-making group (“CODM”), in deciding how to allocate resources and in assessing
performance. The CODM evaluates revenues and gross profits based on product lines and routes to market. Based on our integration and
Management strategies, we operate in two reportable segments, the (i) Infrastructure segment and (ii) Life Sciences segment.
The
Company’s CODM is the Company’s Chief Executive Officer (“CEO”). The CEO reviews financial information presented
on an operating segment basis for purposes of making operating decisions and assessing financial performance. Therefore, and before our
Life Sciences segment started, the Company determined that it operated in a single operating and reportable segment. As of the date of
this report and in preparation for the new and different source of revenue, the Company has determined that it operates in two operating
and reportable segments, the (a) Infrastructure segment and (b) Life Sciences segment. The Company does not include intercompany transfers
between segments for Management reporting purposes.
|
|
December 31, 2024, Form 10-Q |
The
following provides information required by ASC 280-10-50-38 “Entity-wide Information”:
1) The
table below shows revenue reported by segment:
| |
(in thousands) Three months ended December 31,
2024 ($) | | |
(in thousands) Three months ended December 31,
2023 ($) | | |
(in thousands) Nine months ended December 31,
2024 ($) | | |
(in thousands) Nine months ended December 31,
2023 ($) | |
Infrastructure segment | |
| - | | |
| - | | |
| - | | |
| 161 | |
| |
| | | |
| | | |
| | | |
| | |
Life Sciences segment | |
| | | |
| | | |
| | | |
| | |
Wellness and lifestyle | |
| 34 | | |
| 47 | | |
| 101 | | |
| 165 | |
White labeling services | |
| 223 | | |
| 157 | | |
| 841 | | |
| 724 | |
Total | |
| 257 | | |
| 204 | | |
| 941 | | |
| 1,050 | |
For
information on revenue by product and service, refer to Note 2, “Summary of Significant Accounting Policies”.
2)
The table below shows the revenue attributed to the country of domicile (U.S.) and foreign countries. Revenue is generally attributed
to the geographic location of customers:
| |
| |
(in thousands) | |
Segments | |
Country | |
Three months ended December 31, 2024 ($) | | |
Nine months ended December 31, 2024 ($) | |
| |
| |
| | |
| |
Asia | |
India | |
| - | | |
| - | |
America | |
U.S. | |
| 257 | | |
| 939 | |
| |
Colombia | |
| - | | |
| 2 | |
Total | |
| |
| 257 | | |
| 941 | |
| |
| |
(in thousands) | |
Segments | |
Country | |
Three months ended December 31, 2023 ($) | | |
Nine months ended December 31, 2023 ($) | |
| |
| |
| | |
| |
Asia | |
India | |
| - | | |
| 161 | |
America | |
U.S. | |
| 204 | | |
| 889 | |
Total | |
| |
| 204 | | |
| 1,050 | |
|
|
December 31, 2024, Form 10-Q |
3)
The table below shows the non-current assets other than financial instruments held in the country of domicile (U.S.) and foreign countries.
| |
(in thousands) | |
Nature of assets | |
USA (Country of Domicile) ($) | | |
Foreign Countries (India and Colombia) ($) | | |
Total as of December 31, 2024 ($) | |
Intangible assets, net | |
| 1,869 | | |
| - | | |
| 1,869 | |
Property, plant, and equipment, net | |
| 3,295 | | |
| 53 | | |
| 3,348 | |
Claims and advances | |
| 410 | | |
| 271 | | |
| 681 | |
Operating lease asset | |
| 109 | | |
| 20 | | |
| 129 | |
Total non-current assets | |
| 5,683 | | |
| 344 | | |
| 6,027 | |
| |
(in thousands) | |
Nature of assets | |
USA (Country of Domicile) ($) | | |
Foreign Countries (India and Colombia) ($) | | |
Total as of March 31, 2024 ($) | |
Intangible assets, net | |
| 1,616 | | |
| - | | |
| 1,616 | |
Property, plant, and equipment, net | |
| 3,620 | | |
| 75 | | |
| 3,695 | |
Claims and advances | |
| 410 | | |
| 278 | | |
| 688 | |
Operating lease asset | |
| 193 | | |
| 5 | | |
| 198 | |
Total non-current assets | |
| 5,839 | | |
| 358 | | |
| 6,197 | |
NOTE
17 – SUBSEQUENT EVENTS
None.
|
|
December 31, 2024, Form 10-Q |
Item
2. Management’s Discussion and Analysis of Financial Condition and Results of Operations
The
purpose of this Management’s Discussion and Analysis (“MD&A”) is to provide an understanding of IGC Pharma, Inc.’s
(“IGC,” “IGC Pharma,” the “Company,” “we,” “our,” and/or “us”)
consolidated financial condition and results of operations and cash flows. The MD&A should be read in conjunction with our unaudited
condensed financial statements and related notes that appear elsewhere in this Quarterly Report on Form 10-Q for the three months and
nine months ended December 31, 2024, and the Annual Report on Form 10-K for the fiscal year ended March 31, 2024, filed with the SEC
on June 24, 2024 (the “2024 Form 10-K”). The Company’s actual results could differ materially from those discussed
here. Factors that could cause differences include those discussed in the “Forward-Looking Statements” and “Risk Factors”
sections and discussed elsewhere in this report. The risks and uncertainties can cause actual results to differ significantly from those
in our forward-looking statements or implied in historical results and trends. Accordingly, we caution readers not to place undue reliance
on any forward-looking statements made by us, which speak only as of the date they are made. We disclaim any obligation, except as expressly
required by law and the rules of the SEC, to publicly update or revise any such statements to reflect any change in our expectations
or in events, conditions, or circumstances on which any such statements may be based, or that may affect the likelihood that actual results
will differ from those outlined in the forward-looking statements.
Overview
IGC
Pharma is on a mission to transform Alzheimer’s treatment. We are attempting to build a robust pipeline comprising five assets,
each targeting different facets of Alzheimer’s disease at various stages of development. The Alzheimer’s targeting molecule
from each of our platforms is set forth below, the effects of which are subject to clinical trial and investigation:
| ● | IGC-AD1:
Our primary drug candidate, currently undergoing a Phase 2 clinical trial (clinicaltrials.gov, CT05543681), IGC-AD1 holds significant
potential in alleviating the burden of agitation in this vulnerable population. This CB1 partial agonist is specifically designed to
address neuroinflammation associated with agitation in Alzheimer’s patients. |
| ● | TGR-63:
Through pre-clinical studies, TGR-63 has demonstrated its potential to disrupt the progression of Alzheimer’s by targeting Aβ
plaques, a hallmark feature of the disease. This approach offers new avenues for intervening in the underlying pathology of Alzheimer’s. |
| ● | IGC-1C:
At the preclinical stage, we believe IGC-1C represents a forward-thinking approach to Alzheimer’s therapy by targeting tau protein
and neurofibrillary tangles, crucial contributors to the neurodegenerative process. By addressing these pathological mechanisms, IGC-1C
holds potential for disease-modifying interventions. |
| ● | IGC-M3:
Also in preclinical development, IGC-M3 aims to inhibit the aggregation of Aβ plaques, offering potential therapeutic benefits in
early stage Alzheimer’s by targeting the underlying pathology responsible for cognitive decline. |
| ● | LMP:
Designed to target multiple hallmarks of Alzheimer’s disease, including Aβ plaques and neurofibrillary tangles, LMP potentially
represents a comprehensive therapeutic approach to addressing the complex pathophysiology of the disease. |
In
addition to our pipeline of therapeutic candidates, IGC Pharma is attempting to leverage Artificial Intelligence (“AI”) to
develop models for the early detection of Alzheimer’s and to optimize clinical trial design. By integrating cutting-edge technology
with innovative drug development, we are striving to make significant steps in the fight against Alzheimer’s disease.
Furthermore,
IGC controls a total of 30 patent filings reflecting our commitment to innovation and intellectual property protection, including for
IGC-AD1. Our patent portfolio underscores our dedication to safeguarding our competitive advantage in the market.
IGC
Pharma Inc., is a Maryland corporation established in 2005 with a fiscal year ending on March 31, spanning a 52- or 53-week period.
IGC
has two segments: Life Sciences Segment and Infrastructure Segment.
|
|
December 31, 2024, Form 10-Q |
Life
Sciences Segment
IGC
Pharma, a clinical-stage company developing treatments for Alzheimer’s disease, is committed to transforming patient care by striving
to offer faster acting and more effective solutions. Our lead drug, IGC-AD1, embodies this vision by tackling a critical challenge –
managing agitation in Alzheimer’s dementia. Early results from our Phase 2 trial are promising: IGC-AD1 effectively reduced agitation
in patients compared to a placebo, and crucially, it did so much faster than traditional medications. While existing anti-psychotics
can take as long as 6 to 12 weeks to show effects, IGC-AD1 has the potential to act within 2 weeks. This significantly faster onset of
action could significantly improve patient care and represents a potential breakthrough in managing Alzheimer’s-related agitation,
although there can be no assurance thereof. In addition, we have created in-house wellness brands, available through online channels
that are compliant with relevant federal, state, and local laws and regulations. We derive revenue from our in-house wellness non-pharmaceutical
formulations that are manufactured as non-GMO, vegan, products at our facility and are sold over-the-counter (“OTC”).
Infrastructure
Segment
The
Company’s infrastructure business has been operating since 2008, it includes (i) execution of construction contracts and (ii) rental
of heavy construction equipment.
Contract
Research Organization (CRO) and Clinical Trial Software
The
IGC-Pharma Electronic Data Capture system (“IGC-EDC”) is a secure and user-friendly data management software designed to
collect electronic clinical trial data. It includes rigorous security measures to protect data and ensure compliance with regulations.
The system is designed for our Phase 2 trial and can store and organize various handwritten source documents. This allows users to generate
data reports for analysis and computational models to simulate the effects of our investigational drug IGC-AD1.
Recognizing
the importance of operational excellence and cost management in clinical trials, we have established an internal CRO with proprietary
software to reduce trial costs compared to using external CROs. Additionally, we are integrating machine learning and AI into the software
framework for improved decision-making, data entry, computational models, trial design (Phase 3), and data analysis.
Our
Business Strategy
The
business strategy includes:
| ● | Subject
to FDA approval and clinical trials, developing IGC-AD1 as a drug for treating agitation in dementia due to Alzheimer’s. |
| ● | Subject
to FDA approval, developing IGC-AD1 as a drug for treating Alzheimer’s disease. |
| ● | Developing
TGR-63 for the potential treatment of Alzheimer’s disease. |
| ● | Driving
revenue from in-house OTC brands and formulations. |
| ● | Allocate
capital to enhance shareholder value. |
We
believe developing a drug for both symptom and disease-modifying agents has less risk due to the need for expensive multi-year trials.
However, there is considerable upside and significant value creation to the extent we obtain a first-in-class advantage, of which there
can be no assurance. If we were to obtain a first-in-class advantage, such an advantage could result in significant growth if and when
an approved drug such as IGC-AD1 launches.
We
believe that additional investment in clinical trials, AI, R&D, facilities, marketing, advertising, and acquisition of complementary
products and businesses will be critical to the ongoing growth of the Life Sciences segment. Although there can be no assurance, we believe
these investments will fuel the development and delivery of innovative products that drive positive patient and customer experiences.
We hope to leverage our R&D and intellectual property to develop ground-breaking, science-based products that are proven effective
through clinical trials, subject to FDA approval. Although there can be no assurance, we believe this strategy can improve our existing
products and lead to the creation of new products that can provide treatment options for multiple conditions, symptoms, and side effects.
|
|
December 31, 2024, Form 10-Q |
Company
Highlights for the Quarter ended December 31, 2024
| ● | On
December 2, 2024, the Company announced an expansion of its clinical research program for IGC-AD1, an investigational treatment for Alzheimer’s
disease. Building on Phase 2 interim results demonstrating reductions in agitation and cognitive improvement, the Company is initiating
new trials to evaluate IGC-AD1’s potential as a disease-modifying therapy. |
| ● | On
November 25, 2024, the Company announced the expansion of its clinical research program for IGC-AD1, an investigational treatment for
Alzheimer’s disease. |
| ● | On
November 14, 2024, the Company announced additional interim data from its ongoing Phase 2 clinical trial evaluating IGC-AD1. |
| ● | On
October 17, 2024, the Company announced enrollment of patients at the Baycrest Academy for Research and Education in Toronto, Ontario,
Canada, as part of the Company’s ongoing Phase 2 trial investigating IGC-AD1 as a treatment for agitation in Alzheimer’s
dementia. |
| ● | On
October 1, 2024, the Company proudly announced the winning of 2 awards in the PREPARE Challenge (Pioneering Research for Early Prediction
of Alzheimer’s and Related Dementias EUREKA Challenge), with its entry of the Mexican Health and Aging Study (“MHAS”)
database. |
|
|
December 31, 2024, Form 10-Q |
Results
of Operations for the Three Months Ended December 31, 2024, and December 31, 2023
The
historical results presented below are not necessarily indicative of the results that may be expected for any future period. The following
table presents an overview of our results of operations for the three months ended December 31, 2024, and December 31, 2023:
Statement
of Operations (in thousands, unaudited)
| |
Three months ended December 31, | | |
| | |
| |
| |
2024 ($) | | |
2023 ($) | | |
Change ($) | | |
Percent Change | |
Revenue | |
| 257 | | |
| 204 | | |
| 53 | | |
| 26 | % |
Cost of revenue | |
| (153 | ) | |
| (71 | ) | |
| (82 | ) | |
| 115 | % |
Gross profit | |
| 104 | | |
| 133 | | |
| (29 | ) | |
| (22 | )% |
Selling, general and administrative expenses | |
| (1,130 | ) | |
| (2,228 | ) | |
| 1,098 | | |
| (49 | )% |
Research and development expenses | |
| (852 | ) | |
| (903 | ) | |
| 51 | | |
| (6 | )% |
Operating loss | |
| (1,878 | ) | |
| (2,998 | ) | |
| 1,120 | | |
| (37 | )% |
Impairment Loss on PPE | |
| - | | |
| (2,623 | ) | |
| 2,623 | | |
| (100 | )% |
Other income, net | |
| 49 | | |
| 32 | | |
| 17 | | |
| 53 | % |
Loss before income taxes | |
| (1,829 | ) | |
| (5,589 | ) | |
| 3,760 | | |
| (67 | )% |
Income tax expense/benefit | |
| - | | |
| - | | |
| - | | |
| - | |
Net loss | |
| (1,829 | ) | |
| (5,589 | ) | |
| 3,760 | | |
| (67 | )% |
Revenue
– Revenue was approximately $257 thousand and $204 thousand for the three months ended December 31, 2024, and December 31,
2023, respectively. Revenue in both quarters was primarily derived from our Life Sciences segment, which involved providing white-label
manufactured products and sales of holistic health care products, among others. The increase in revenue is attributed to the white-label
project in the U.S. The Company is committed to its current strategy of driving sales in formulations both as branded and white-labeled
products in the Life Science segment.
Cost
of revenue – Cost of revenue amounted to approximately $153 thousand for the three months ended December 31, 2024, compared
to $71 thousand in the three months ended December 31, 2023, this represents gross margins of 40% and 65%, respectively. The cost of
revenue is primarily attributable to the cost of raw materials, labor, and other direct overheads required to produce our products in
the Life Science segment. Typically, the gross margin in the Life Sciences business will fluctuate from one quarter to another based
on the mix within the Life Sciences business between white label, private label, and branded products. There is insufficient revenue
to model or project gross margins.
Selling,
general and administrative expenses (“SG&A”)– SG&A expenses primarily encompass various costs
such as employee-related expenses, sales commissions, professional fees, legal fees, marketing expenses, other corporate expenses, allocated
general overhead, provisions, depreciation, and write-offs related to doubtful accounts and advances. During the three months ended December
31, 2024, SG&A expenses decreased by approximately $1.1 million or 49% to approximately $1.0 million, from approximately $2.2 million
recorded for the three months ended December 31, 2023. The decrease of $1.1 million is attributed to a one-time expense of approximately
$734 thousand during the three months ended December 31, 2023, and the focus of management on cost efficiency in marketing and corporate
expenses during the three months ended December 31, 2024.
Research
and development expenses (“R&D”)– R&D expenses were attributed to our Life Sciences segment.
The R&D expenses decreased by approximately $51 thousand or 6% to approximately $852 thousand during the three months ended December
31, 2024, from approximately $903 thousand. It is primarily attributable to the progression of Phase 2 trials on IGC-AD1 and pre-clinical
studies on the other small molecule assets. We anticipate increased R&D expenses as the development of our other small molecule assets
targeting Alzheimer’s and the Phase 2 trial on Alzheimer’s expand.
Impairment
Loss – During the three months ended December 31, 2024, there was no impairment loss on PPE. During the three months ended
December 31, 2023, the Company impaired the land situated in Nagpur, India, by approximately $2.6 million to $1.5 million from $4.1 million
to bring it closer to the fair value.
Other
income, net – Other net income increased by approximately $17 thousand or 53% during the thousand months ended December 31,
2024. As a result, the total other income for the three months ended December 31, 2024, and 2023, is approximately $49 thousand and $32
thousand, respectively. Other income includes interest and rental income, profit from the sale of assets, unrealized gains from investments,
and one-time awards or prizes, among others.
|
|
December 31, 2024, Form 10-Q |
Results
of Operations for the Nine Months Ended December 31, 2024, and December 31, 2023
The
historical results presented below are not necessarily indicative of the results that may be expected for any future period. The following
table presents an overview of our results of operations for the nine months ended December 31, 2024, and December 31, 2023:
Statement
of Operations (in thousands, unaudited)
| |
Nine months ended December 31, | | |
| | |
| |
| |
2024 ($) | | |
2023 ($) | | |
Change ($) | | |
Percent Change | |
Revenue | |
| 941 | | |
| 1,050 | | |
| (109 | ) | |
| (10 | )% |
Cost of revenue | |
| (476 | ) | |
| (488 | ) | |
| 12 | | |
| (2 | )% |
Gross profit | |
| 465 | | |
| 562 | | |
| (97 | ) | |
| (17 | )% |
Selling, general and administrative expenses | |
| (3,841 | ) | |
| (5,272 | ) | |
| 1,431 | | |
| (27 | )% |
Research and development expenses | |
| (2,658 | ) | |
| (2,918 | ) | |
| 260 | | |
| (9 | )% |
Operating loss | |
| (6,034 | ) | |
| (7,628 | ) | |
| 1,594 | | |
| (21 | )% |
Impairment Loss on PPE | |
| - | | |
| (2,623 | ) | |
| 2,623 | | |
| (100 | )% |
Other income, net | |
| 110 | | |
| 136 | | |
| (26 | ) | |
| (19 | )% |
Loss before income taxes | |
| (5,924 | ) | |
| (10,115 | ) | |
| 4,191 | | |
| (41 | )% |
Income tax expense/benefit | |
| - | | |
| - | | |
| - | | |
| - | |
Net loss | |
| (5,924 | ) | |
| (10,115 | ) | |
| 4,191 | | |
| (41 | )% |
Revenue
– Revenue was approximately $941 thousand and $1.0 million for the nine months ended December 31, 2024, and December 31, 2023,
respectively. Revenue in both quarters was primarily derived from our Life Sciences segment, which involved providing white-label manufactured
products and sales of holistic health care products, among others. The decrease in revenue is attributed to the completion of our Infrastructure
project in India. Revenue from life science segment increased by approximately by $52 thousand during nine months ended December 31,
2024. The Company is committed to its current strategy of driving sales in formulations both as branded and white-labeled products in
the Life Science segment.
Cost
of revenue – Cost of revenue amounted to approximately $476 thousand for the nine months ended December 31, 2024, compared
to $488 thousand in the nine months ended December 31, 2023, this represents gross margins of 49% and 54%, respectively. The cost of
revenue is primarily attributable to the cost of raw materials, labor, and other direct overheads required to produce our products in
the Life Science segment. Typically, the gross margin in the Life Sciences business will fluctuate from one quarter to another based
on the mix within the Life Science business between white label, private label, and branded products. There is insufficient revenue to
model or project gross margins.
SG&A
– SG&A expenses primarily encompass various costs such as employee-related expenses, sales commissions, professional fees,
legal fees, marketing expenses, other corporate expenses, allocated general overhead, provisions, depreciation, and write-offs related
to doubtful accounts and advances. During the nine months ended December 31, 2024, SG&A expenses decreased by approximately $1.4
million or 27% to approximately $3.8 million during the nine months ended December 31, 2024, from approximately $5.3 million. The decrease
of $1.4 million is attributed to a one-time expense of approximately $734 thousand during the nine months ended December 31, 2023, and
the focus of management on cost efficiency in marketing and corporate expenses during the nine months ended December 31, 2024.
R&D
– R&D expenses were attributed to our Life Sciences segment. The R&D expenses decreased by approximately $260 thousand
or 9% to approximately $2.6 million during the nine months ended December 31, 2024, from approximately $2.9 million. It is primarily
attributable to the progression of Phase 2 trials on IGC-AD1 and pre-clinical studies on the other small molecule assets. We anticipate
increased R&D expenses as the development of our other small molecule assets targeting Alzheimer’s and the Phase 2 trial on
Alzheimer’s expand.
Impairment
Loss – During the nine months ended December 31, 2024, there was no impairment loss on PPE. During the nine months ended December
31, 2023, the Company impaired the land situated in Nagpur, India, by approximately $2.6 million to $1.5 million from $4.1 million to
bring it closer to the fair value.
Other
income, net – Other net income decreased by approximately $26 thousand or 19% during the thousand nine months ended December
31, 2024. As a result, the total other income for the nine months ended December 31, 2024, and 2023 is approximately $110 thousand and
$136 thousand, respectively. Other income includes interest and rental income, profit from the sale of assets, unrealized gains from
investments, and one-time awards or prizes, among others.
|
|
December 31, 2024, Form 10-Q |
Liquidity
and Capital Resources
Our
sources of liquidity are cash and cash equivalents, funds raised through the ATM offering, cash flows from operations, short-term and
long-term borrowings, and short-term liquidity arrangements. The Company continues to evaluate various financing sources and options
to raise working capital to help fund current research and development programs and operations. The Company does not have any material
long-term debt, capital lease obligations, or other long-term liabilities except as disclosed in this report. Please refer to Note 12,
“Commitments and Contingencies,” and Note 11, “Loans and Other Liabilities,” in Item 1 of this report for further
information on Company commitments and contractual obligations.
Pursuant
to the signed Master Loan and Security Agreement (the “Credit Agreement”) with O-Bank, Co., Ltd., the Company successfully
obtained a working capital credit facility totaling $12 million and, in addition, signed two SPAs to raise $6 million in exchange for
approximately 18.8 million shares. The equity and the credit facility serve to minimize ongoing liquidity requirements and ensure the
Company’s ability to sustain its operations. Furthermore, the Company intends to raise additional funds through private placement
and ATM offerings, subject to market conditions, although there can be no assurance that such financing efforts will be successful or
as to any private placement the of terms of such offering. Please refer to Note 13 – “Securities”, for more information.
On
July 29, 2024, the Company entered into an amendment to extend the Credit Agreement with O-Bank, Co., Ltd., effective July 8, 2024. The
amendment extends the term of the Credit Agreement, which was set to expire, under the same terms and conditions as previously disclosed
on the Company’s Current Report on Form 8-K filed with the Securities Exchange Commission on July 7, 2023, with the exception of
a reduction in the facility fees from $120,000 to $84,000. All other material terms of the Credit Agreement remain unchanged.
On
October 27, 2023, the Company entered into a Sales Agreement (the “Agreement”) with A.G.P./Alliance Global Partners (the
“Agent”) pursuant to which the Company may offer and sell, from time to time, through the Agent, as sales agent and/or principal,
shares of its common stock, par value $0.0001 per share (the “Common Stock”), having an aggregate offering price of up to
$60 million (“Shares”), subject to certain limitations on the amount of Common Stock that may be offered and sold by the
Company set forth in the Sales Agreement (the “Offering”).
On
March 22, 2024, the Company entered into a Share Purchase Agreement (the “March 2024 SPA”) with Bradbury Strategic Investment
Fund A, resulting in approximately $3 million in gross proceeds. During the quarter ended June 30, 2024, the Company issued approximately
8.8 million shares of unregistered common stock at a price of $0.34 per share. Shares are intended to be exempt from registration under
the Securities Act of 1933, as amended (the “Securities Act”), by virtue of the provisions of Section 4(a)(2) of the Securities
Act and Regulation D and/or Regulation S adopted thereunder. During fiscal 2024, the Company had received $500 thousand of the total
$3 million due under the March 2024 SPA, while the remaining $2.5 million was received in April 2024.
On
September 25, 2024, the Company entered into the 2024 Share Purchase Agreement (the “September 2024 SPA”) with Moran Global
Strategies, Inc., a Virginia corporation (“MGS”), which is owned by James Moran, a director of IGC, relating to the sale
and issuance by our company to the investors of an aggregate of 588,235 shares of our common stock, for a total purchase price of $200,000,
or $0.34 per share, subject to the terms and conditions set forth in the September 2024 SPA. The investment is subject to customary closing
conditions, including NYSE approval. As per the September 2024 SPA, the investor received piggyback registration rights subject to certain
restrictions.
|
|
December 31, 2024, Form 10-Q |
The
Company expects to raise further capital for its research and development initiatives as and when it is able to do so, but there can
be no assurance thereof. In addition, there can be no assurance of the terms thereof, and any subsequent equity financing sought may
have dilutive effects on our current shareholders. While there is no guarantee that we will be successful, we are applying to non-dilutive
funding opportunities such as Small Business Research and Development programs. In addition, subject to limitations on the amount of
capital that can be raised, the Company expects to utilize its shelf registration on a statement on Form S- 3 to raise capital through
at-the-market offerings or otherwise.
| |
(in thousands, unaudited) | | |
| | |
| |
| |
As of December 31, 2024 ($) | | |
As of March 31, 2024 ($) | | |
Change | | |
Percent Change | |
Cash and cash equivalents | |
| 470 | | |
| 1,198 | | |
| (728 | ) | |
| (61 | )% |
Working capital | |
| 394 | | |
| 1,365 | | |
| (971 | ) | |
| (71 | )% |
Cash
and cash equivalents
Cash
and cash equivalents decreased by approximately $728 thousand to $470 thousand in the nine months ended December 31, 2024, from $1.2
million as of March 31, 2024, and a decrease of approximately 61%. The decrease of approximately $728 thousand is attributable to the
Company’s operational and R&D expenses.
Summary
of Cash flows
| |
(in thousands, unaudited) | | |
| | |
| |
| |
Nine months ended December 31, | | |
| | |
Percent | |
| |
2024 | | |
2023 | | |
Change | | |
Change | |
Cash used in operating activities | |
| (4,065 | ) | |
| (4,673 | ) | |
| 608 | | |
| (13 | )% |
Cash (used in) provided by investing activities | |
| (300 | ) | |
| 6 | | |
| (306 | ) | |
| (5,097 | )% |
Cash provided by financing activities | |
| 3,646 | | |
| 2,857 | | |
| 789 | | |
| 28 | % |
Effects of exchange rate changes on cash and cash equivalents | |
| (9 | ) | |
| (8 | ) | |
| (1 | ) | |
| 100 | % |
Net increase (decrease) in cash and cash equivalents | |
| (728 | ) | |
| (1,818 | ) | |
| 1,090 | | |
| (60 | )% |
Cash and cash equivalents at the beginning of period | |
| 1,198 | | |
| 3,196 | | |
| (1,998 | ) | |
| (63 | )% |
Cash and cash equivalents at the end of the period | |
| 470 | | |
| 1,378 | | |
| (908 | ) | |
| (66 | )% |
Operating
Activities
Net
cash used in operating activities for the nine months ended December 31, 2024, was approximately $4.1 million. It consists of a net loss
of approximately $5.9 million, a positive impact on cash due to non-cash expenses of approximately $1.6 million, and a positive change
in operating assets and liabilities of approximately $224 thousand. Non-cash expenses consist of an amortization and depreciation charge
of approximately $464 thousand and stock-based expenses of approximately $1.2 million. In addition, changes in operating assets and liabilities
had a positive impact of approximately $224 thousand on cash, of which a net negative impact of approximately $190 thousand is due to
an increase in deposits and advances, and a positive impact of approximately $251 thousand is due to increase in accrued and other liabilities,
a net positive impact of approximately $107 thousand is due to an increase in inventory and net other current assets and liabilities
of approximately $56 thousand.
Net
cash used in operating activities for the nine months ended December 31, 2023, was approximately $4.6 million. It consists of a net loss
of approximately $10.1 million, a positive impact on cash due to non-cash expenses of approximately $5.2 million, and a positive change
in operating assets and liabilities of approximately $220 thousand. Non-cash expenses consist of an amortization and depreciation charge
of approximately $473 thousand, stock-based expenses of approximately $1.4 million, impairment loss of approximately $3.3 million and
an approximately $42 thousand decrease in other non-cash items. In addition, changes in operating assets and liabilities had a positive
impact of approximately $220 thousand on cash, of which approximately $169 thousand is due to a decrease in deposits and advances, approximately
$117 thousand increase in accounts payable, approximately $83 thousand decrease in accrued and other liabilities and approximately $20
thousand increase in other net current assets and liabilities.
|
|
December 31, 2024, Form 10-Q |
Investing
Activities
Net
cash used in investing activities for the nine months ended December 31, 2024, was approximately $300 thousand, which is comprised of
expenses of approximately $252 thousand for the acquisition, and development of intangible assets, and approximately $78 thousand for
the net purchase of property, plant, and equipment.
Net
cash provided by investing activities for the nine months ended December 31, 2023, was approximately $6 thousand, which comprised of
expenses of approximately $67 thousand for the acquisition filing expenses related to intellectual property, approximately $81 thousand
for the net purchase of property, plant, and equipment and approximately $154 thousand of investment in marketable securities.
Financing
Activities
Net
cash provided by financing activities was approximately $3.6 million for the nine months ended December 31, 2024, which is comprised
of net proceeds from issuance of equity stock of approximately $3.6 million, and offset by the re-payment of the loan of approximately
$3 thousand. Please refer to Note 13 – “Securities”, for more information.
Net
cash provided by financing activities was approximately $2.9 million for the nine months ended December 31, 2023, which is comprised
of net proceeds from issuance of equity stock of approximately $2.8 million and re-payment of the loan of approximately $3 thousand.
|
|
December 31, 2024, Form 10-Q |
Off-Balance
Sheet Arrangements
We
do not have any outstanding derivative financial instruments, off-balance sheet guarantees, interest rate swap transactions, or foreign
currency forward contracts. Furthermore, we do not have any retained or contingent interest in assets transferred to an unconsolidated
entity that serves as credit, liquidity, or market risk support to such entity. We do not have any variable interest in an unconsolidated
entity that provides financing, liquidity, market risk, or credit support to us or that engages in leasing, hedging, or research and
development services with us.
Critical
Accounting Policies
While
all accounting policies impact financial statements, certain policies may be viewed as critical. Critical accounting policies are those
that are both most important to the portrayal of financial condition and results of operations and that require management’s most
subjective or complex judgments and estimates. Our management believes the policies that fall within this category are the policies on
revenue recognition, inventory, accounts receivable, foreign currency translation, impairment of long-lived assets and investments, stock-based
compensation, and cybersecurity.
Please
see our disclosures in Note 2 – Summary of Significant Accounting Policies to the Notes to the Unaudited Condensed Consolidated
Financial Statements in this report, in the Notes to the Audited Consolidated Financial Statements in the 2024 Form 10-K, as well as
Item 7 – Management’s Discussion and Analysis of Financial Condition and Results of Operations in the 2024 Form 10-K, for
a discussion of all our critical and significant accounting policies.
Recent
Accounting Pronouncements
Changes
to U.S. GAAP are established by the Financial Accounting Standards Board (“FASB”) in the form of accounting standards updates
(“ASUs”) to the FASB’s Accounting Standards Codification. The Company considers the applicability and impact of all
ASUs. Newly issued ASUs not listed are expected to have no impact on the Company’s consolidated financial position and results
of operations because either the ASU is not applicable, or the impact is expected to be immaterial. Recent accounting pronouncements
that may apply to us are described in Note 2, “Significant Accounting Policies” to the Notes to the Unaudited Condensed Consolidated
Financial Statements in this report and in the Notes to the Audited Consolidated Financial Statements in Part II of our 2024 Form 10-K.
|
|
December 31, 2024, Form 10-Q |
Item
3. Quantitative and Qualitative Disclosures about Market Risk
Item
3 does not apply to us because we are a smaller reporting company.
Item
4. Controls and Procedures
Evaluation
of Disclosure Controls and Procedures
Our
Management maintains disclosure controls and procedures as defined in Rule 13a-15(e) and 15d-15(e) under the Securities Exchange Act
of 1934 (the “Exchange Act”) that are designed to provide reasonable assurance that information required to be disclosed
in our reports filed or submitted under the Exchange Act is processed, recorded, summarized and reported within the time periods specified
in the SEC’s rules and forms and that such information is accumulated and communicated to Management, including our Chief Executive
Officer (our principal executive officer) and Principal Financial Officer, as appropriate, to allow for timely decisions regarding required
disclosure.
Our
Management, including the Chief Executive Officer and Principal Financial Officer, conducted an evaluation of the effectiveness of our
disclosure controls and procedures as of the end of the period covered by this report. Based on this evaluation, our Chief Executive
Officer and Principal Financial Officer concluded that our disclosure controls and procedures were effective in ensuring that the information
required to be disclosed in the reports filed or submitted by us under the Exchange Act was recorded, processed, summarized and reported
within the requisite time periods specified in SEC rules and forms and that such information was accumulated and communicated to our
Management, including our Chief Executive Officer and Principal Financial Officer, as appropriate to allow for timely decisions regarding
required disclosure.
Changes
in Internal Control over Financial Reporting
Our
Management, including our Chief Executive Officer and Principal Financial Officer, evaluated our “internal control over financial
reporting” as defined in Exchange Act Rule 13a-15(f) to determine whether any changes in our internal control over financial reporting
occurred during the three months ended December 31, 2024, that materially affected, or are reasonably likely to materially affect, our
internal control over financial reporting. Based on that evaluation, there were no changes in our internal control over financial reporting
during the three months ended December 31, 2024, that have materially affected or are reasonably likely to materially affect our internal
control over financial reporting.
|
|
December 31, 2024, Form 10-Q |
PART
II – OTHER INFORMATION
Item
1. Legal Proceedings
The
Company may be involved in legal proceedings, claims, and assessments arising in the ordinary course of business. Such matters are subject
to many uncertainties, and outcomes are not predictable with assurance. As of December 31, 2024, we were not party to any material legal
proceedings other than disclosed below.
During
the fiscal quarter ended December 31, 2024, the following material litigation is pending:
Engineering
and Consulting Group SAS et al. v IGC Pharma Inc., case file no. 110016000050202247710 (Prosecutor’s Office 393 Sectional Economic
Crimes Unit, Bogota, Colombia). The Company and the ECG corporation are in a contractual dispute. The Company filed a complaint against
four (4) individuals with the Prosecutor’s Office 393 Sectional Economic Crimes Unit, Bogota, Colombia, under file no. 110016000050202247710
for charges of fraud, falsification of a private document, and conspiracy to commit a crime. The complaint was filed in 2022. In December
2023, the case was reviewed by the investigator and scheduled and accepted for a hearing by the prosecutor in calendar 2024. In the quarter,
the Company met with the prosecutors and pressed the urgency of moving the case through the legal system.
Item
1A. Risk Factors
There
have been no material changes to the risk factors disclosed in Part I, Item 1A, “Risk Factors” in our Annual Report on Form
10-K for the year ended March 31, 2024, filed with the SEC on June 24, 2024.
Item
2. Unregistered Sales of Equity Securities and Use of Proceeds
None.
Item
3. Defaults Upon Senior Securities
None.
Item
4. Mine Safety Disclosures
Not
applicable.
Item
5. Other Information
None.
|
|
December 31, 2024, Form 10-Q |
Item
6. Exhibits
Exhibit |
|
Number |
Exhibit
Description |
3.1 |
Amended and Restated Articles of Incorporation of the Registrant, as amended on August 1, 2012 (incorporated by reference to Exhibit 3.1 to the Company’s Current Report on Form 8-K filed on August 6, 2012). |
3.2 |
Articles of Amendment to the Company’s Amended and Restated Articles of Incorporation filed with the State Department of Assessments and Taxation of Maryland on March 7, 2023 (incorporated by reference to Exhibit 3.1 to the Company’s Current Report on Form 8-K filed on March 21, 2023). |
3.3 |
By-laws of the Registrant (incorporated by reference to Exhibit 3.2 to the Company’s Post-Effective Amendment No.1 to Form S-3 filed on January 22, 2021). |
3.4 |
Amendment to the Amended and Restated Articles of Incorporation of the Registrant as amended on August 2, 2014 (incorporated by reference to Exhibit 3.3 to the Company’s Post-Effective Amendment No.1 to Form S-3 filed on January 22, 2021). |
3.5 |
Amendment to the Bylaws of the Company dated March 2, 2023 (incorporated by reference to Exhibit 3.2 to the Company’s Current Report on Form 8-K filed on March 21, 2023). |
31.1* |
Rule 13a-14(a) / 15d-14(a) Certification of Chief Executive Officer. |
31.2* |
Rule 13a-14(a) / 15d-14(a) Certification of Principal Financial Officer. |
32.1** |
Certifications pursuant to 18 U.S.C. §1350. |
101.INS* |
Inline
XBRL Instance Document. |
101.SCH* |
Inline
XBRL Taxonomy Extension Schema Document. |
101.CAL* |
Inline
XBRL Taxonomy Extension Calculation Linkbase Document. |
101.LAB* |
Inline
XBRL Taxonomy Extension Label Linkbase Document. |
101.PRE* |
Inline
XBRL Taxonomy Extension Presentation Linkbase Document. |
101.DEF* |
Inline
XBRL Taxonomy Extension Definition Linkbase Document. |
104* |
Cover
Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101). |
| † | Certain
schedules or similar attachments to this exhibit have been omitted in accordance with Item 601(a)(5) of Regulation S-K. |
|
|
December 31, 2024, Form 10-Q |
SIGNATURES
Pursuant
to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by
the undersigned thereunto duly authorized.
|
IGC
PHARMA, INC. |
|
|
|
Date:
February 14, 2025 |
By: |
/s/
Ram Mukunda |
|
|
Ram
Mukunda |
|
|
President
and Chief Executive Officer
(Principal
Executive Officer) |
|
|
|
Date:
February 14, 2025 |
By: |
/s/
Claudia Grimaldi |
|
|
Claudia
Grimaldi |
|
|
Vice-president
& Chief Compliance Officer
(Principal
Financial Officer) |
|
|
December 31, 2024, Form 10-Q |
0001326205
false
2025
Q3
--03-31
0001326205
2024-04-01
2024-12-31
0001326205
2025-02-10
0001326205
2024-12-31
0001326205
2024-03-31
0001326205
2024-10-01
2024-12-31
0001326205
2023-10-01
2023-12-31
0001326205
2023-04-01
2023-12-31
0001326205
us-gaap:CommonStockMember
2023-09-30
0001326205
us-gaap:CommonStockIncludingAdditionalPaidInCapitalMember
2023-09-30
0001326205
us-gaap:RetainedEarningsMember
2023-09-30
0001326205
us-gaap:AccumulatedOtherComprehensiveIncomeMember
2023-09-30
0001326205
2023-09-30
0001326205
us-gaap:CommonStockMember
2023-10-01
2023-12-31
0001326205
us-gaap:CommonStockIncludingAdditionalPaidInCapitalMember
2023-10-01
2023-12-31
0001326205
us-gaap:RetainedEarningsMember
2023-10-01
2023-12-31
0001326205
us-gaap:AccumulatedOtherComprehensiveIncomeMember
2023-10-01
2023-12-31
0001326205
us-gaap:CommonStockMember
2023-12-31
0001326205
us-gaap:CommonStockIncludingAdditionalPaidInCapitalMember
2023-12-31
0001326205
us-gaap:RetainedEarningsMember
2023-12-31
0001326205
us-gaap:AccumulatedOtherComprehensiveIncomeMember
2023-12-31
0001326205
2023-12-31
0001326205
us-gaap:CommonStockMember
2024-09-30
0001326205
us-gaap:CommonStockIncludingAdditionalPaidInCapitalMember
2024-09-30
0001326205
us-gaap:RetainedEarningsMember
2024-09-30
0001326205
us-gaap:AccumulatedOtherComprehensiveIncomeMember
2024-09-30
0001326205
2024-09-30
0001326205
us-gaap:CommonStockIncludingAdditionalPaidInCapitalMember
2024-10-01
2024-12-31
0001326205
us-gaap:CommonStockMember
2024-10-01
2024-12-31
0001326205
us-gaap:RetainedEarningsMember
2024-10-01
2024-12-31
0001326205
us-gaap:AccumulatedOtherComprehensiveIncomeMember
2024-10-01
2024-12-31
0001326205
us-gaap:CommonStockMember
2024-12-31
0001326205
us-gaap:CommonStockIncludingAdditionalPaidInCapitalMember
2024-12-31
0001326205
us-gaap:RetainedEarningsMember
2024-12-31
0001326205
us-gaap:AccumulatedOtherComprehensiveIncomeMember
2024-12-31
0001326205
us-gaap:CommonStockMember
2023-03-31
0001326205
us-gaap:CommonStockIncludingAdditionalPaidInCapitalMember
2023-03-31
0001326205
us-gaap:RetainedEarningsMember
2023-03-31
0001326205
us-gaap:AccumulatedOtherComprehensiveIncomeMember
2023-03-31
0001326205
2023-03-31
0001326205
us-gaap:CommonStockMember
2023-04-01
2023-12-31
0001326205
us-gaap:CommonStockIncludingAdditionalPaidInCapitalMember
2023-04-01
2023-12-31
0001326205
us-gaap:RetainedEarningsMember
2023-04-01
2023-12-31
0001326205
us-gaap:AccumulatedOtherComprehensiveIncomeMember
2023-04-01
2023-12-31
0001326205
us-gaap:CommonStockMember
2024-03-31
0001326205
us-gaap:CommonStockIncludingAdditionalPaidInCapitalMember
2024-03-31
0001326205
us-gaap:RetainedEarningsMember
2024-03-31
0001326205
us-gaap:AccumulatedOtherComprehensiveIncomeMember
2024-03-31
0001326205
us-gaap:CommonStockIncludingAdditionalPaidInCapitalMember
2024-04-01
2024-12-31
0001326205
us-gaap:CommonStockMember
2024-04-01
2024-12-31
0001326205
us-gaap:RetainedEarningsMember
2024-04-01
2024-12-31
0001326205
us-gaap:AccumulatedOtherComprehensiveIncomeMember
2024-04-01
2024-12-31
0001326205
igc:InfrastructureSegmentMember
2024-10-01
2024-12-31
0001326205
igc:InfrastructureSegmentMember
2023-10-01
2023-12-31
0001326205
igc:InfrastructureSegmentMember
2024-04-01
2024-12-31
0001326205
igc:InfrastructureSegmentMember
2023-04-01
2023-12-31
0001326205
igc:WellnessAndLifestyleMember
2024-10-01
2024-12-31
0001326205
igc:WellnessAndLifestyleMember
2023-10-01
2023-12-31
0001326205
igc:WellnessAndLifestyleMember
2024-04-01
2024-12-31
0001326205
igc:WellnessAndLifestyleMember
2023-04-01
2023-12-31
0001326205
igc:WhiteLabelingServicesMember
2024-10-01
2024-12-31
0001326205
igc:WhiteLabelingServicesMember
2023-10-01
2023-12-31
0001326205
igc:WhiteLabelingServicesMember
2024-04-01
2024-12-31
0001326205
igc:WhiteLabelingServicesMember
2023-04-01
2023-12-31
0001326205
igc:ClinicalTrialInventoryMember
2024-03-31
0001326205
igc:ClinicalTrialInventoryMember
2024-12-31
0001326205
us-gaap:PatentsMember
2024-12-31
0001326205
us-gaap:PatentsMember
2024-03-31
0001326205
us-gaap:OtherIntangibleAssetsMember
2024-12-31
0001326205
us-gaap:OtherIntangibleAssetsMember
2024-03-31
0001326205
us-gaap:PatentsMember
2024-12-31
0001326205
us-gaap:PatentsMember
2024-03-31
0001326205
us-gaap:SoftwareDevelopmentMember
2024-12-31
0001326205
us-gaap:SoftwareDevelopmentMember
2024-03-31
0001326205
us-gaap:LandMember
2023-04-01
2024-03-31
0001326205
igc:PropertyPlantAndEquipmentTableMember
2024-04-01
2024-12-31
0001326205
us-gaap:BuildingAndBuildingImprovementsMember
2024-12-31
0001326205
us-gaap:BuildingAndBuildingImprovementsMember
2024-03-31
0001326205
srt:MinimumMember
us-gaap:MachineryAndEquipmentMember
2024-12-31
0001326205
srt:MaximumMember
us-gaap:MachineryAndEquipmentMember
2024-12-31
0001326205
us-gaap:MachineryAndEquipmentMember
2024-12-31
0001326205
us-gaap:MachineryAndEquipmentMember
2024-03-31
0001326205
us-gaap:ComputerEquipmentMember
2024-12-31
0001326205
us-gaap:ComputerEquipmentMember
2024-03-31
0001326205
srt:MinimumMember
us-gaap:OfficeEquipmentMember
2024-12-31
0001326205
srt:MaximumMember
us-gaap:OfficeEquipmentMember
2024-12-31
0001326205
us-gaap:OfficeEquipmentMember
2024-12-31
0001326205
us-gaap:OfficeEquipmentMember
2024-03-31
0001326205
us-gaap:FurnitureAndFixturesMember
2024-12-31
0001326205
us-gaap:FurnitureAndFixturesMember
2024-03-31
0001326205
us-gaap:VehiclesMember
2024-12-31
0001326205
us-gaap:VehiclesMember
2024-03-31
0001326205
us-gaap:LandMember
2024-04-01
2024-12-31
0001326205
2020-06-11
0001326205
2020-06-11
2020-06-11
0001326205
2023-06-30
0001326205
srt:MaximumMember
2024-04-01
2024-12-31
0001326205
srt:MinimumMember
2024-04-01
2024-12-31
0001326205
igc:March2024SPAMember
2024-03-22
2024-03-22
0001326205
igc:March2024SPAMember
2024-04-01
2024-06-30
0001326205
igc:March2024SPAMember
2024-06-30
0001326205
igc:March2024SPAMember
2023-04-01
2024-03-31
0001326205
igc:March2024SPAMember
2024-04-01
2024-04-30
0001326205
us-gaap:InvestorMember
igc:September2024SPAMember
2024-09-25
2024-09-25
0001326205
igc:ESOP2008OmnibusPlanMember
2024-12-31
0001326205
igc:ESOP2008OmnibusPlanMember
2024-04-01
2024-12-31
0001326205
us-gaap:GeneralAndAdministrativeExpenseMember
2024-04-01
2024-12-31
0001326205
us-gaap:EmployeeStockOptionMember
us-gaap:GeneralAndAdministrativeExpenseMember
2024-04-01
2024-12-31
0001326205
us-gaap:GeneralAndAdministrativeExpenseMember
2023-04-01
2023-12-31
0001326205
us-gaap:EmployeeStockOptionMember
us-gaap:GeneralAndAdministrativeExpenseMember
2023-04-01
2023-12-31
0001326205
us-gaap:EmployeeStockOptionMember
us-gaap:GeneralAndAdministrativeExpenseMember
2024-12-31
0001326205
2023-04-01
2024-03-31
0001326205
us-gaap:FairValueInputsLevel1Member
us-gaap:CashAndCashEquivalentsMember
2024-04-01
2024-12-31
0001326205
us-gaap:FairValueInputsLevel1Member
us-gaap:CashAndCashEquivalentsMember
2024-12-31
0001326205
us-gaap:FairValueInputsLevel1Member
us-gaap:MoneyMarketFundsMember
2024-04-01
2024-12-31
0001326205
us-gaap:FairValueInputsLevel1Member
us-gaap:MoneyMarketFundsMember
2024-12-31
0001326205
us-gaap:FairValueInputsLevel1Member
igc:DebtFundsMember
2024-04-01
2024-12-31
0001326205
us-gaap:FairValueInputsLevel1Member
igc:DebtFundsMember
2024-12-31
0001326205
us-gaap:FairValueInputsLevel1Member
us-gaap:MutualFundMember
2024-04-01
2024-12-31
0001326205
us-gaap:FairValueInputsLevel1Member
us-gaap:MutualFundMember
2024-12-31
0001326205
us-gaap:FairValueInputsLevel2Member
us-gaap:CertificatesOfDepositMember
2024-04-01
2024-12-31
0001326205
us-gaap:FairValueInputsLevel2Member
us-gaap:CertificatesOfDepositMember
2024-12-31
0001326205
us-gaap:FairValueInputsLevel3Member
2024-04-01
2024-12-31
0001326205
us-gaap:FairValueInputsLevel3Member
2024-12-31
0001326205
us-gaap:FairValueInputsLevel1Member
us-gaap:CashAndCashEquivalentsMember
2023-04-01
2024-03-31
0001326205
us-gaap:FairValueInputsLevel1Member
us-gaap:CashAndCashEquivalentsMember
2024-03-31
0001326205
us-gaap:FairValueInputsLevel1Member
us-gaap:MoneyMarketFundsMember
2023-04-01
2024-03-31
0001326205
us-gaap:FairValueInputsLevel1Member
us-gaap:MoneyMarketFundsMember
2024-03-31
0001326205
us-gaap:FairValueInputsLevel1Member
igc:DebtFundsMember
2023-04-01
2024-03-31
0001326205
us-gaap:FairValueInputsLevel1Member
igc:DebtFundsMember
2024-03-31
0001326205
us-gaap:FairValueInputsLevel1Member
us-gaap:MutualFundMember
2023-04-01
2024-03-31
0001326205
us-gaap:FairValueInputsLevel1Member
us-gaap:MutualFundMember
2024-03-31
0001326205
us-gaap:FairValueInputsLevel2Member
us-gaap:CertificatesOfDepositMember
2023-04-01
2024-03-31
0001326205
us-gaap:FairValueInputsLevel2Member
us-gaap:CertificatesOfDepositMember
2024-03-31
0001326205
us-gaap:FairValueInputsLevel3Member
2023-04-01
2024-03-31
0001326205
us-gaap:FairValueInputsLevel3Member
2024-03-31
0001326205
igc:LegacyInfrastructureMember
2024-10-01
2024-12-31
0001326205
igc:LegacyInfrastructureMember
2023-10-01
2023-12-31
0001326205
igc:LegacyInfrastructureMember
2024-04-01
2024-12-31
0001326205
igc:LegacyInfrastructureMember
2023-04-01
2023-12-31
0001326205
country:IN
2024-10-01
2024-12-31
0001326205
country:IN
2024-04-01
2024-12-31
0001326205
country:US
2024-10-01
2024-12-31
0001326205
country:US
2024-04-01
2024-12-31
0001326205
country:CO
2024-10-01
2024-12-31
0001326205
country:CO
2024-04-01
2024-12-31
0001326205
country:IN
2023-10-01
2023-12-31
0001326205
country:IN
2023-04-01
2023-12-31
0001326205
country:US
2023-10-01
2023-12-31
0001326205
country:US
2023-04-01
2023-12-31
0001326205
us-gaap:GeographicDistributionDomesticMember
2024-12-31
0001326205
us-gaap:GeographicDistributionForeignMember
2024-12-31
0001326205
us-gaap:GeographicDistributionDomesticMember
2024-03-31
0001326205
us-gaap:GeographicDistributionForeignMember
2024-03-31
xbrli:shares
iso4217:USD
iso4217:USD
xbrli:shares
xbrli:pure