Notes to Condensed
Consolidated
Financial Statements
(Unaudited
)
1.
Description of Business and Basis of Presentation
Organization and Basis of Presentation
Cesca Therapeutics Inc. (“Cesca Therapeutics,” “Cesca,” the “Company,” “we,” “our,” “us”), a Delaware corporation, is a regenerative medicine company that was founded in 1986 and is headquartered in Rancho Cordova, CA. We develop, commercialize and market a range of automated technologies and products for cell-based therapeutics. ThermoGenesis Corp. (“ThermoGenesis”), our device
subsidiary, provides the AutoXpress
®
and BioArchive platforms for automated clinical biobanking, PXP™ platform for point-of-care cell-based therapies and CAR-TXpress™ platform under development for bio-manufacturing for immuno-oncology applications. Cesca is also leveraging its proprietary PXP™ technology platform to develop autologous cell-based therapies that address significant unmet needs in the vascular and orthopedic markets.
Cesca is an affiliate of the Boya
life Group, a China-based industry research alliance encompassing top research institutions for stem cell and regenerative medicine.
Liquidit
y
T
he Company has a Revolving Credit Agreement (“Credit Agreement”) with Boyalife Investment Fund II, Inc. (the “Lender”) (Refer to Note 4). As of September 30, 2017, the Company had drawn down $5,000,000 of the $10,000,000 available under the Credit Agreement. Boyalife Investment Fund II, Inc. is a wholly owned subsidiary of Boyalife Group Inc., which is owned and controlled by the Company’s Chief Executive Officer and Chairman of the Board.
On July 7, 2017, the Company, through its wholly-owned subsidiary, ThermoGenesis, acquired the business and substantially all the assets of SynGen Inc. (“SynGen”). In exchange, ThermoGenesis issued to SynGen shares of ThermoGenesis common stock that, after giving effect to the issuance, constitute 20% of ThermoGenesis
’ outstanding common shares, and ThermoGenesis also made a one-time cash payment of $1,000,000 to SynGen. (Refer to Note 3).
At September
30, 2017, the Company had cash and cash equivalents of $2,464,000 and working capital of $5,312,000. The Company has incurred recurring operating losses and as of September 30, 2017 had an accumulated deficit of $187,707,000. The Company anticipates requiring additional capital to grow the device business (see Note 8), initiate the Phase III Critical Limb Ischemia trial, to fund other operating expenses and to make interest payments on the line of credit with Boyalife. These conditions raised substantial doubt about the Company’s ability to meet its obligations. To alleviate the substantial doubt, management plans to use existing cash and cash equivalents balances, revenue generating activities and draw down on the available balance from the line of credit. Other sources of liquidity could include potential issuances of debt or equity securities in public or private financings and strategic partnerships.
Based upon the additional funds available to draw down under the amended Credit Agreement, the Company
’s cash balance, historical trends, expected outflows and projections for revenues, management believes it will have sufficient cash to provide for its projected needs to maintain operations and working capital requirements for at least the next 12 months from the date of this filing.
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements
(Continued)
(Unaudited)
Principles of Consolidation
The consolidated financial statements include the accounts of Cesca
, its majority-owned subsidiary, ThermoGenesis, and its wholly-owned subsidiaries, TotipotentRX Cell Therapy, Pvt. Ltd. and TotipotentSC Scientific Product Pvt. Ltd. All significant intercompany accounts and transactions have been eliminated upon consolidation.
Noncontrolling Interests
The 20% ownership interest of
ThermoGenesis that is not owned by Cesca, is accounted for as a non-controlling interest as the Company has an 80% ownership interest in the subsidiary. Earnings or losses attributable to other stockholders of a consolidated affiliated company are classified separately as "noncontrolling interest" in the Company's consolidated statements of operations. Net loss attributable to noncontrolling interest reflects only its share of the after-tax earnings or losses of an affiliated company. The Company's consolidated balance sheets reflect noncontrolling interests within the equity section of the consolidated balance sheets.
Interim Reporting
The a
ccompanying unaudited condensed consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States (“U.S. GAAP”) for interim financial information and with the instructions to Form 10-Q and Article 10 of Regulation S-X. Accordingly, certain information and footnote disclosures normally included in annual financial statements prepared in accordance with U.S. GAAP have been condensed or omitted pursuant to such Securities and Exchange Commission (“SEC”) rules and regulations and accounting principles applicable for interim periods. In the opinion of management, all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation have been included. Events subsequent to the balance sheet date have been evaluated for inclusion in the accompanying condensed consolidated financial statements through the date of issuance. Operating results for the three month period ended September 30, 2017 are not necessarily indicative of the results that may be expected for the six months ending December 31, 2017. These unaudited condensed consolidated financial statements should be read in conjunction with the consolidated financial statements and the notes thereto included in the Annual Report on Form 10-K for the fiscal year ended June 30, 2017.
2.
Summary of Significant Accounting Policies
Revenue Recognition
Revenues from the sale of
the Company’s products and services are recognized when persuasive evidence of an arrangement exists, delivery has occurred (or services have been rendered), the price is fixed or determinable, and collectability is reasonably assured. The Company generally ships products F.O.B. shipping point. There is no conditional evaluation on any product sold and recognized as revenue. Amounts billed in excess of revenue recognized are recorded as deferred revenue on the balance sheet.
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements
(Continued)
(Unaudited)
There is no right of return provided for distributors
or customers. For sales of products made to distributors, the Company considers a number of factors in determining whether revenue is recognized upon transfer of title to the distributor, or when payment is received. These factors include, but are not limited to, whether the payment terms offered to the distributor are considered to be non-standard, the distributor history of adhering to the terms of its contractual arrangements with the Company, the level of inventories maintained by the distributor, whether the Company has a pattern of granting concessions for the benefit of the distributor, and whether there are other conditions that may indicate that the sale to the distributor is not substantive. The Company currently recognizes revenue primarily on the sell-in method with its distributors.
Revenue arrangements with multiple deliverables are divided into units of accounting if certain criteria are met, including whether the deliverable item(s) has (have) value to the customer on a stand-alone basis. Revenue for each unit of accounting is recognized as the unit of accounting is delivered. Arrangement consideration is allocated to each unit of accounting based upon the relative estimated selling prices of the separate units of accounting contained within an arrangement containing multiple deliverables. Estimated selling prices are determined using vendor specific objective evidence of value (
“VSOE”), when available, or an estimate of selling price when VSOE is not available for a given unit of accounting. Significant inputs for the estimates of the selling price of separate units of accounting include market and pricing trends and a customer’s geographic location. The Company accounts for training and installation, and service agreements and the collection, processing and testing of the umbilical cord blood and the storage as separate units of accounting.
Service revenue generated from contracts for providing maintenance of equipment is amortized over the life of the agreement.
Revenue generated from storage contracts is deferred and recorded ratably over the life of the agreement, up to 21 years.
All other service revenue is recognized at the time the service is completed.
Revenues are net of normal discounts. Shipping and handling fees billed to customers are included in net revenues, while the related costs are included in cost of revenues.
Fair Value
Measurements
In accordance with ASC 820, “
Fair Value Measurements and Disclosures
,” fair value is defined as the exit price, or the amount that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants as of the measurement date.
The guidance also establishes a hierarchy for inputs used in measuring fair value that maximizes the use of observable inputs and minimizes the use of unobservable inputs by requiring that the most observable inputs be used when available. Observable inputs are inputs
that market participants would use in valuing the asset or liability and are developed based on market data obtained from sources independent of the Company. Unobservable inputs are inputs that reflect the Company’s assumptions about the factors that market participants would use in valuing the asset or liability. The guidance establishes three levels of inputs that may be used to measure fair value:
|
Level 1:
|
Quoted market prices in active markets for identical assets or liabilities.
|
|
Level 2:
|
Observable market-based inputs or unobservable inputs that are corroborated by market data.
|
|
Level 3:
|
Unobservable inputs reflecting the reporting entity
’s own assumptions.
|
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements
(Continued)
(Unaudited)
The carrying values of cash and cash equivalents, accounts receivabl
e and accounts payable approximate fair value due to their short duration. The fair value of the Company’s derivative obligation liability is classified as Level 3 within the fair value hierarchy since the valuation model of the derivative obligation is based on unobservable inputs.
Segment Reporting
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 (“CODM”), or decision making group, whose function is to allocate resources to and assess the performance of the operating
segments. The Company has identified its chief executive officer and chief operating officer as the CODM. In determining its reportable segments, the Company considered the markets and the products or services provided to those markets.
The Company has two reportable business segments:
|
●
|
T
he Clinical Development Division, is devel
op
ing autologous (utilizing the patient’s own cells) stem cell-based
therapeutics
that address significant unmet medical needs for applications within the
vascular, cardiology and orthopedic
markets.
|
|
●
|
T
he Device Division, engages in the development and commercialization of automated technologies for c
ell-based t
herapeutics
and bio-processing. The device division is operated through the Company’s ThermoGenesis subsidiary.
|
Net Loss per Share
Net loss per share is computed by dividing the net loss by the weighted average number of common shares outstanding. The calculation
of the basic and diluted earnings per share is the same for all periods presented, as the effect of the potential common stock equivalents is anti-dilutive due to the Company’s net loss position for all periods presented. Anti-dilutive securities consisted of the following at September 30:
|
|
2017
|
|
|
2016
|
|
Vested Series A warrants
|
|
|
404,412
|
|
|
|
404,412
|
|
Unvested Series A warrants
(1)
|
|
|
698,529
|
|
|
|
698,529
|
|
Warrants
– other
|
|
|
3,725,782
|
|
|
|
3,725,782
|
|
Stock options
|
|
|
420,185
|
|
|
|
270,016
|
|
Restricted stock units
|
|
|
9,163
|
|
|
|
161,170
|
|
Total
|
|
|
5,258,071
|
|
|
|
5,259,909
|
|
|
(1)
|
The unvested Series A warrants were subject to vesting based upon the amount of funds actually received
by the Company in the second close of the August 2015 financing which never occurred. The warrants will remain outstanding but unvested until they expire in February 2021
.
|
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements
(Continued)
(Unaudited)
Recently
Adopted Accounting Standards
In March 2016, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) 2016-09, “
Compensation - Stock Compensation (Topic 718): Improvements to Employee Share-Based Payment Accounting”.
ASU 2016-09 simplifies several aspects of the accounting for share-based payment award transactions, including: (a) income tax consequences; (b) classification of awards as either equity or liabilities; and (c) classification on the statement of cash flows. The Company adopted ASU 2016-09 effective July 1, 2017. The Company has elected to continue its current policy of estimating forfeitures rather than recognizing forfeitures when they occur. Adoption of the new standard did not have a material impact on the financial statements of the Company.
In July 2015, the FASB issued ASU No. 2015-11, “
Inventory: Simplifying the Measurement of Inventory
”, that requires inventory not measured using either the last in, first out (“LIFO”) or the retail inventory method to be measured at the lower of cost and net realizable value. Net realizable value is the estimated selling price in the ordinary course of business, less reasonably predictable cost of completion, disposal and transportation. The Company adopted ASU 2015-11 effective July 1, 2017. Adoption of the new standard did not have a material impact on the financial statements of the Company.
Recently Issued Accounting
Standards
In May 2014, the FASB issued ASU 2014-09, “
Revenue from Contracts with Customers (Topic 606)
” (“ASU 2014-09”). ASU 2014-09 supersedes the revenue recognition requirements in ASC Topic 605, “Revenue Recognition” and some cost guidance included in ASC Subtopic 605-35, "
Revenue Recognition
- Construction-Type and Production-Type Contracts
.” The core principle of ASU 2014-09 is that revenue is recognized when the transfer of goods or services to customers occurs in an amount that reflects the consideration to which the Company expects to be entitled in exchange for those goods or services. ASU 2014-09 requires the disclosure of sufficient information to enable readers of the Company’s financial statements to understand the nature, amount, timing and uncertainty of revenue and cash flows arising from customer contracts. ASU 2014-09 also requires disclosure of information regarding significant judgments and changes in judgments, and assets recognized from costs incurred to obtain or fulfill a contract. ASU 2014-09 provides two methods of retrospective application. The first method would require the Company to apply ASU 2014-09 to each prior reporting period presented. The second method would require the Company to retrospectively apply ASU 2014-09 with the cumulative effect recognized at the date of initial application. ASU 2014-09 will be effective for the Company beginning in fiscal 2018 as a result of ASU 2015-14, "
Revenue from Contracts with Customers (Topic 606): Deferral of the Effective Date
," which was issued by the FASB in August 2015 and extended the original effective date by one year. The Company is currently evaluating the impact of adopting the available methodologies of ASU 2014-09 and 2015-14 upon its financial statements in future reporting periods. The Company is also in the process of evaluating the new standard against its existing accounting policies, including the timing of revenue recognition, and its contracts with customers to determine the effect the guidance will have on its financial statements and what changes to systems and controls may be warranted.
3.
Acquisition
of SynGen
On July 7, 2017, Cesca, through its then wholly-owned subsidiary ThermoGenesis, entered into an Asset Acquisition Agreement (the “Asset Acquisition Agreement”) with SynGen, and pursuant to the terms of the Asset Acquisition Agreement, ThermoGenesis acquired on July 7, 2017 substantially all of SynGen
’s operating assets, including its proprietary cell processing platform technology (the “Transaction”).
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements (Continued)
(Unaudited)
The business acquired in the Transaction excludes certain assets and liabilities of SynGen that ThermoGenesis did not acquire under the Asset Acquisition Agreement including cash and cash equivalents, accounts receivable, certain prepaid expenses and other current assets, other assets, accounts payable and other accrued liabilities
. The acquisition was consummated for the purpose of enhancing the Company’s cord blood product portfolio and settling litigation between the Company and SynGen.
The acquisition was accounted for under the acquisition method of accounting for business combinations which requires, among other things that the assets acquired and liabilities assumed be recognized at their fair values as of the acquisition date. Acquisition-related costs are not included as a component of the acquisition accounting, but are recognized as expenses in the periods in which the costs are incurred. Acquisition related costs of $
187,000 for the three months ended September 30, 2017 were included in general and administrative expenses. Subsequent to July 7, 2017, Cesca has recorded revenues of approximately $47,000 associated with the operations of SynGen. The amount of net loss specifically related to SynGen operations for the period beginning July 7, 2017, included in the condensed consolidated statements of operations and comprehensive loss is impracticable due to the fact that SynGen and its operations are no longer accounted for on a stand-alone basis.
The consideration for t
he Transaction consisted of $1,000,000 in cash and ThermoGenesis’ issuance at closing to SynGen of an aggregate of 2,000,000 shares of its common stock, constituting a 20% interest, which had a fair market value of $2,499,000. All outstanding SynGen stock options to purchase shares of SynGen common stock were cancelled.
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements (Continued)
(Unaudited)
Preliminary Allocation of Consideration Transferred to Net Assets Acquired
The following is the summary of the preliminary fair value of the assets acquired and the liabilities assumed by Cesca in the Transaction, reconciled to the consideration transferred.
ThermoGenesis
issued 2,000,000 shares of its common stock that had a total fair value of $2,499,000 based on an independent valuation. The final determination of the fair value of certain assets and liabilities will be completed within the 12-month measurement period from the date of acquisition as required. It is anticipated that the goodwill will be deductible for tax purposes. Any potential adjustments made could be material in relation to the preliminary values presented below:
Purchase Price:
|
|
|
|
|
|
|
|
|
|
|
|
|
Cash
|
|
|
|
|
|
|
|
|
|
$
|
1,000,000
|
|
2,000,000 common shares of ThermoGenesis
|
|
|
|
|
|
|
|
|
|
|
2,499,000
|
|
Fair value of assets acquired:
|
|
|
|
|
|
|
|
|
|
|
|
|
Inventories
|
|
|
|
|
|
|
649,000
|
|
|
|
|
|
Developed technology
|
|
|
318,000
|
|
|
|
|
|
|
|
|
|
Trade name
|
|
|
26,000
|
|
|
|
|
|
|
|
|
|
In process technology
|
|
|
1,296,000
|
|
|
|
|
|
|
|
|
|
Customer relationships
|
|
|
41,000
|
|
|
|
|
|
|
|
|
|
Total intangible assets
|
|
|
|
|
|
|
1,681,000
|
|
|
|
|
|
Property and equipment
|
|
|
|
|
|
|
585,000
|
|
|
|
|
|
Total assets
|
|
|
|
|
|
|
2,915,000
|
|
|
|
|
|
Fair value of liabilities assumed:
|
|
|
|
|
|
|
|
|
|
|
|
|
Other liabilities
|
|
|
|
|
|
|
15,000
|
|
|
|
|
|
Net assets acquired
|
|
|
|
|
|
|
|
|
|
|
(2,900,000
|
)
|
Preliminary goodwill
|
|
|
|
|
|
|
|
|
|
$
|
599,000
|
|
Supplemental Pro Forma Data
The Company used the acquisition method of accounting to account for the
SynGen acquisition and, accordingly, the results of SynGen are included in the Company’s consolidated financial statements for the period subsequent to the date of acquisition. The following unaudited supplemental pro forma data for the quarters ended September 30, 2017 and 2016 present consolidated information as if the acquisition had been completed on July 1, 2016. The pro forma results were calculated by combining the results of Cesca Inc with the stand-alone results of SynGen Inc. for the pre-acquisition periods:
|
|
Three Months Ended
September 30,
|
|
|
|
2017
|
|
|
2016
|
|
Net revenues
|
|
$
|
3,069,000
|
|
|
$
|
4,078,000
|
|
Net loss
|
|
$
|
(2,439,000
|
)
|
|
$
|
(23,141,000
|
)
|
Basic and diluted net loss per common share
|
|
$
|
(0.22
|
)
|
|
$
|
(3.80
|
)
|
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements
(Continued)
(Unaudited)
The unaudited pro forma financial information reflects certain adjustments related to the acquisition, such as the incremental amortization expense in connection with recording acquired identifiable intangible assets at fair value,
the revised payroll expense associated with the new salaries of SynGen employees resulting from the merger, the elimination of SynGen expenses related to debt issuance costs, interest and other warrant related expenses, the elimination of the legal fees paid by both parties related to the litigation between Cesca and SynGen as ceasing the litigation was part of the Asset Acquisition Agreement and costs directly related to the acquisition.
4
.
Related Party Transactions
Revolving Credit Agreement
On March 6, 2017, Cesca entered into the Credit Agreement with Boyalife Investment Fund II, Inc. (the “Lender”). The Lender is a wholly owned subsidiary of Boyalife Group Inc., which is owned and controlled by the Company
’s Chief Executive Officer and Chairman of the Board of Directors. The Credit Agreement grants to the Company the right to borrow up to $5,000,000 in amounts of $500,000 per advance on an unsecured basis (the “Loan”) at any time prior to March 6, 2022 (the “Maturity Date”). The Company has drawn down a total of $5,000,000 as of September 30, 2017.
The Credit Agreement and the Convertible Promissory Note issued thereunder (the “Note”) provide that the principal and all accrued and unpaid interest under the Loan will be due and payable on the Maturity Date, with payments of interest-only due on the last day of each calendar year. The Loan bears interest at 22% per annum, simple interest, except that certain borrowed amounts used to pay legal expenses under the bill payment arrangement will not bear interest. The Note can be prepaid in whole or in part by the Company at any time without penalty. If the Note is not repaid in full on or before the Maturity Date, the Lender has the right after the Maturity Date to convert any unpaid principal and accrued interest into shares of the Company
’s common stock at a conversion price equal to 90% of the average daily volume-weighted average trading price of the Company’s common stock during the 10 trading days immediately prior to the Maturity Date, provided that the number of shares issuable upon such conversion may not exceed 19.99% of the number of outstanding shares of common stock of the Company on the date of the Credit Agreement (unless the Company obtains stockholder approval for such issuance in the manner required by the Marketplace Rules of the Nasdaq Stock Market, Inc.).
On September 13, 2017, the Company entered into Amendment No. 1 to the Credit Agreement (the “Amended Credit Agreement”). The Amended Credit Agreement amends the Credit Agreement originally entered into by the Company and Lender on March 6, 2017, by increasing the Company
’s maximum borrowing availability thereunder from $5,000,000 to $10,000,000. In connection with such amendment, the Company and Lender entered into an amended and restated convertible promissory note to reflect the new aggregate maximum principal amount of $10,000,000.
The Maturity Date of the Note is subject to acceleration at the option of the Lender upon customary events of default, which include a breach of the Loan documents, termination of operations, or bankruptcy. The Lender
’s obligation to make advances under the Loan is subject to the Company’s representations and warranties in the Credit Agreement continuing to be true at all times and there being no continuing event of default under the Note. The Credit Agreement provides that if the Lender at any time in the future purchases the Company’s blood and bone marrow processing device business, the Lender would refund to the Company legal fees expended by the Company in connection with certain litigation expenses funded by the Company with proceeds of the Loan. No default has occurred through the date of filing.
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements
(Continued)
(Unaudited)
The Company recorded interest expense of $
197,000 for the three months ended September 30, 2017 and had an interest payable balance of $319,000 and $122,000 at September 30, 2017 and June 30, 2017, respectively.
Distributo
r Agreement
On August 21, 2017, ThermoGenesis entered into an International Distributor Agreement with Boyalife W.S.N. Under the terms of the agreement, Boyalife W.S.N. was granted the exclusive right, subject to existing distributors and customers (if any), to develop, sell to, and service a customer base for ThermoGenesis
’ AXP
®
(“AutoXpress
®
”
) System and BioArchive
®
System in the People’s Republic of China (excluding Hong Kong and Taiwan), Singapore, Indonesia, and the Philippines (the “Territories”). Boyalife W.S.N. is an affiliate of our Chief Executive Officer and Chairman of our Board of Directors, and Boyalife (Hong Kong) Limited, our largest stockholder. Boyalife W.S.N,’s rights under the agreement include the exclusive right to distribute AXP
®
Disposable Blood Processing Sets and use rights to the AXP
®
(“AutoXpress
®
”
) System, BioArchive System and other accessories used for the processing of stem cells from cord blood in the Territories. Boyalife W.S.N. is also appointed as the exclusive service provider to provide repairs and preventative maintenance to ThermoGenesis products in the Territories.
The term of the agreement is for three years with ThermoGenesis having the right to renew the agreement for successive two-year periods at its option. However, ThermoGenesis has the right to terminate the agreement early if Boyalife W.S.N. fails to meet specified minimum purchase requirements.
Revenues
During the three months ended September 30, 2017, the Company recorded $751,000
of revenues from Boyalife and had an accounts receivable balance of $751,000 and $308,000 at September 30, 2017 and June 30, 2017, respectively.
Bill Payment Arrangement
The Company entered into a bill payment arrangement whereby Boyalife Group Ltd. (“Payor”), the Company
’s largest shareholder, agreed to pay the Company’s legal expenses payable to the Company’s attorney related to certain litigation involving SynGen Inc. (the “Bill Payment Arrangement”), although the Company remains jointly and severally liable for the payment of such legal fees. The terms of the Bill Payment Arrangement provided that the Company will reimburse Payor for any and all amounts paid by Payor in connection with the Bill Payment Arrangement under certain specified events. There is no interest payable on outstanding balance of related party payable. This litigation was terminated as part of the SynGen acquisition agreement. As of September 30, 2017, invoices totaling $606,000 had been paid by Payor and are included in related party payable as the Company anticipates repaying this within a year.
5
.
Commitments
and Contingencies
Financial Covenants
Effective
May 15, 2017, the Company entered into a Sixth Amended and Restated Technology License and Escrow Agreement with CBR Systems, Inc. which modified the financial covenant that the Company must meet in order to avoid an event of default. The Company must maintain a cash balance and short-term investments net of debt or borrowed funds that are payable within one year of not less than $2,000,000. The Company was in compliance with this financial covenant as of September 30, 2017.
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements
(Continued)
(Unaudited)
Warranty
The Company
offers a warranty on all of its non-disposable products of one to two years. The Company warrants disposable products through their expiration date. The Company periodically assesses the adequacy of its recorded warranty liabilities and adjusts the amounts as necessary.
The warranty liability is included in other current liabilitie
s in the unaudited balance sheets. The change in the warranty liability for the three months ended September 30, 2017 is summarized in the following table:
Balance
at July 1, 2017
|
|
$
|
588,000
|
|
Warranties issued during the period
|
|
|
40,000
|
|
Settlements made during the period
|
|
|
(297,000
|
)
|
Changes in liability for pre-existing warranties during the period
|
|
|
(4,000
|
)
|
Balance at
September 30, 2017
|
|
$
|
327,000
|
|
Contingency
In fiscal 2016, the Company signed an engagement letter with a strategic consulting firm. Included in the engagement letter was a success fee due upon the successful conclusion of certain strategic
transactions. On May 4, 2017, a lawsuit was filed against the Company and its CEO by the consulting firm as the consulting firm argues that it is owed a transaction fee of $1,000,000 under the terms of the engagement letter due to the conversion of the Boyalife debentures in August 2016. In October 2017, to streamline the case and without acknowledging any liability, the Company deposited $1,000,000 with the Court and the consulting firm is in the process of dismissing the Company’s CEO from the case, without liability. The Company intends to defend the lawsuit vigorously and no accrual has been recorded for this contingent liability as of September 30, 2017.
6
.
Derivative Obligation
s
Series A Warrants
Series A warrants to purchase 404,412 common shares were issued and vested during the year ended June 30, 2016. At the time of issuance, the Company determined that as such warrants can be settled for cash at the holders
’ option in a future fundamental transaction they constituted a derivative liability. The Company has estimated the fair value of the derivative liability, using a Binomial Lattice Valuation Model and the following assumptions:
|
|
Series A
|
|
|
|
September 30,
2017
|
|
|
June 30,
2017
|
|
Market price of common stock
|
|
$
|
3.56
|
|
|
$
|
3.17
|
|
Expected volatility
|
|
|
102
|
%
|
|
|
110
|
%
|
Contractual term (years)
|
|
|
3.4
|
|
|
|
3.7
|
|
Discount rate
|
|
|
1.7
|
%
|
|
|
1.66
|
%
|
Dividend rate
|
|
|
0
|
%
|
|
|
0
|
%
|
Exercise price
|
|
$
|
8.00
|
|
|
$
|
8.00
|
|
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements
(Continued)
(Unaudited)
Expected volatilities are based on the historical volatility of the Company
’s common stock. Contractual term is based on remaining term of the respective warrants. The discount rate represents the yield on U.S. Treasury bonds with a maturity equal to the contractual term.
The Company recorded a
loss of $13,000 and $326,000 during the three months ended September 30, 2017 and 2016, respectively, representing the net change in the fair value of the derivative liability, which is presented as fair value change of derivative instruments, in the accompanying consolidated statements of operations and comprehensive loss.
T
he following table represents the Company’s fair value hierarchy for its financial liabilities measured at fair value on a recurring basis as of September 30, 2017 and June 30, 2017:
|
|
Balance at September
30,
2017
|
|
|
Level 1
|
|
|
Level 2
|
|
|
Level 3
|
|
Derivative obligation
|
|
$
|
743,000
|
|
|
$
|
-
|
|
|
$
|
-
|
|
|
$
|
743,000
|
|
|
|
Balance at June
30,
2017
|
|
|
Level 1
|
|
|
Level 2
|
|
|
Level 3
|
|
Derivative obligation
|
|
$
|
730,000
|
|
|
$
|
-
|
|
|
$
|
-
|
|
|
$
|
730,000
|
|
The following table reflects the change in fair value of the Company
’s derivative liabilities for the three months ended September 30, 2017:
|
|
Amount
|
|
Balance
– July 1, 2017
|
|
$
|
730,000
|
|
Change in fair value of derivative obligation
|
|
|
13,000
|
|
Balance
– September 30, 2017
|
|
$
|
743,000
|
|
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements
(Continued)
(Unaudited)
7
.
Stockholders
’
Equity
Stock Based Compensation
The Company
recorded stock-based compensation of $132,000 and $298,000 for the three months ended September 30, 2017 and 2016, respectively.
The following is a summary of option activity for
the Company’s stock option plans:
|
|
Number of
Shares
|
|
|
Weighted-
Average
Exercise
Price
|
|
|
Weighted-
Average
Remaining
Contractual
Life
|
|
|
Aggregate
Intrinsic
Value
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Outstanding at June 30,
2017
|
|
|
397,389
|
|
|
$
|
5.80
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Granted
|
|
|
40,000
|
|
|
$
|
3.47
|
|
|
|
|
|
|
|
|
|
Forfeited
|
|
|
(14,765
|
)
|
|
$
|
3.52
|
|
|
|
|
|
|
|
|
|
Expired
|
|
|
(2,439
|
)
|
|
$
|
27.04
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Outstanding at
September 30, 2017
|
|
|
420,185
|
|
|
$
|
5.54
|
|
|
|
6
|
|
|
$
|
182,000
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Vested and expected to v
est at September 30, 2017
|
|
|
397,590
|
|
|
$
|
5.66
|
|
|
|
6
|
|
|
$
|
175,000
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Exercisable at
September 30, 2017
|
|
|
278,487
|
|
|
$
|
6.64
|
|
|
|
5.5
|
|
|
$
|
128,000
|
|
The aggregate intrinsic value is calculated as the difference between the exercise price of the underlying awards and the quoted price of the Company
’s common stock. There were no options exercised during the three months ended September 30, 2017.
The fair value of the Company
’s stock options granted for the three months ended September 30, 2017 was estimated using the following weighted-average assumptions:
Expected life (years)
|
|
|
4
|
|
Risk-free interest rate
|
|
|
1.7
|
%
|
Expected volatility
|
|
|
108
|
%
|
Dividend yield
|
|
|
0
|
%
|
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements
(Continued)
(Unaudited)
Common Stock Restricted
Units
The following is a summary of
restricted stock activity during the three months ended September 30, 2017:
|
|
|
|
|
|
Weighted
Average
|
|
|
|
Number of
Shares
|
|
|
Grant Date
Fair Value
|
|
Balance at June 30,
2017
|
|
|
59,694
|
|
|
$
|
4.62
|
|
Granted
|
|
|
10,000
|
|
|
$
|
3.26
|
|
Vested
|
|
|
(60,531
|
)
|
|
$
|
4.54
|
|
Forfeited
|
|
|
--
|
|
|
|
--
|
|
Outstanding at September 30, 201
7
|
|
|
9,163
|
|
|
$
|
3.65
|
|
Warrants
There was
no warrant activity for the three months ended September 30, 2017. At September 30, 2017, there were 4,828,723 warrants outstanding with a weighted-average exercise price per share of $9.37 and 4,130,192 warrants exercisable with a weighted-average exercise price per share of $9.60.
At September 30, 2017, the total intrinsic value of warrants outstanding and exercisable was $0.
8
.
Segment Reporting
The
Company has two reportable segments, which are the same as its operating segments:
The Clinical Development
segment is developing autologous (utilizing the patient’s own cells) stem cell-based therapeutics that address significant unmet medical needs for applications within the vascular, cardiology and orthopedic markets.
The
device segment is a pioneer and market leader in the development and commercialization of
automated technologies for c
ell-based t
herapeutics
and bio-processing.
Cesca Therapeutics Inc.
Notes to Condensed Consolidated Financial Statements
(Continued)
(Unaudited)
The following table summarizes the operating results of the Company
’s reportable segments:
|
|
Three Months Ended September 30, 2017
|
|
|
|
Clinical
Development
|
|
|
Device
|
|
|
Total
|
|
Net revenues
|
|
$
|
126,000
|
|
|
$
|
2,943,000
|
|
|
$
|
3,069,000
|
|
Cost of revenues
|
|
|
120,000
|
|
|
|
2,018,000
|
|
|
|
2,138,000
|
|
Gross profit
|
|
|
6,000
|
|
|
|
925,000
|
|
|
|
931,000
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Operating expenses
|
|
|
1,169,000
|
|
|
|
2,112,000
|
|
|
|
3,281,000
|
|
Operating loss
|
|
$
|
(1,163,000
|
)
|
|
$
|
(1,187,000
|
)
|
|
$
|
(2,350,000
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Depreciation and amortization
|
|
$
|
75,000
|
|
|
$
|
85,000
|
|
|
$
|
160,000
|
|
Stock-based compensation expense
|
|
$
|
85,000
|
|
|
$
|
47,000
|
|
|
$
|
132,000
|
|
|
|
Three Months Ended September 30, 2016
|
|
|
|
Clinical
Development
|
|
|
Device
|
|
|
Total
|
|
Net revenues
|
|
$
|
156,000
|
|
|
$
|
3,611,000
|
|
|
$
|
3,767,000
|
|
Cost of revenues
|
|
|
142,000
|
|
|
|
2,243,000
|
|
|
|
2,385,000
|
|
Gross profit
|
|
|
14,000
|
|
|
|
1,368,000
|
|
|
|
1,382,000
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Operating expenses
|
|
|
1,964,000
|
|
|
|
1,366,000
|
|
|
|
3,330,000
|
|
Operating profit (loss)
|
|
$
|
(1,950,000
|
)
|
|
$
|
2,000
|
|
|
$
|
(1,948,000
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Depreciation and amortization
|
|
$
|
139,000
|
|
|
$
|
122,000
|
|
|
$
|
261,000
|
|
Stock-based compensation expense
|
|
$
|
190,000
|
|
|
$
|
108,000
|
|
|
$
|
298,000
|
|