Gain Therapeutics, Inc. (Nasdaq: GANX) (“Gain”, or the “Company”),
a clinical-stage biotechnology company leading the discovery and
development of the next generation of allosteric small molecule
therapies, today announced financial results for the third quarter
ended September 30, 2023, and highlighted recent corporate
progress.
“With the compelling preclinical data we
presented at the International Congress of Parkinson’s Disease and
Movement Disorders and the initiation of our Phase 1 clinical trial
of GT-02287, we have made tremendous progress this past quarter,”
said Matthias Alder, Chief Executive Officer of Gain Therapeutics.
“Dose escalation continues as planned, and we look forward to
providing updates on the study in the first half of next year.”
Pipeline Updates
- Presentation of late
breaking preclinical data at the International Congress of
Parkinson's Disease and Movement Disorders in Copenhagen,
Denmark: Gain presented data from two distinct preclinical
models of Parkinson’s disease (PD) demonstrating that the
administration of GT-02287 resulted in restored GCase function and
a significant reduction of the pathological hallmarks and motor
dysfunction associated with Parkinson’s disease. In addition, the
data presented in the poster accepted as a late breaking abstract
demonstrated that administration of GT-02287 led to a significant
reduction of plasma levels of the emerging neurodegeneration
biomarker neurofilament light chain (NfL) in an animal model of
GBA1-PD, providing direct evidence of the neuroprotective effect
and the potential of GT-02287 to slow or even stop the progression
of Parkinson’s disease;
- Commencement of Phase 1
Clinical Trial: Gain received approval from the Bellberry
Human Research Ethics Committee (HREC) in Australia to initiate a
Phase 1 clinical study of GT-02287 evaluating safety, tolerability,
pharmacokinetics, and pharmacodynamics measured by blood levels of
glucocerebrosidase (GCase) activity, a readout which may provide
early clinical proof of concept. Dosing of the first two subjects
occurred in September, and dose escalation is ongoing;
- Research collaborators of
Gain link GCase dysfunction to lysosomal accumulation of Tau
protein, suggesting a role in both Parkinson’s (PD) and Alzheimer’s
disease (AD): In a paper published in Nature Scientific
Reports, Gain collaborators at the Institute for Research in
Biomedicine and the NeuroCenter of Southern Switzerland of EOC have
shown that GCase and lysosomal dysfunction is associated with tau
accumulation. This provides further scientific validation of the
potential of GT-02287 to provide a disease-modifying treatment not
only in Parkinson’s disease but also tauopathies such as
Alzheimer’s disease.
Upcoming Milestones
- Completion of the single ascending
dose part of the Phase 1 clinical trial of GT-02287 expected late
Q4 or early Q1 2024, with demonstration of safety and tolerability
of GT-02287 after single administration.
- Completion of the multiple
ascending dose part of the Phase 1 clinical trial of GT-02287
expected in Q2 2024, with demonstration of safety and tolerability
of GT-02287 after 14-day treatment, and the potential to provide
early clinical proof-of-concept of GT-02287 target engagement in
human subjects.
- Initiation of first-in-patient
proof of concept study in H2 2024, with demonstration of safety and
tolerability of GT-02287 in Parkinson’s patients after 3-month
treatment, and the potential to provide biomarker-based clinical
proof-of-concept of GT-02287.
Financial Results
Research and development (R&D)
expenses totaled $2.4 million for the three months ended
September 30, 2023, compared to $2.0 million for the same period in
2022. The $0.4 million increase in R&D expense was primarily
due to increases in costs associated with clinical and preclinical
studies, quality and manufacturing as Gain’s GBA1 PD program
entered a Phase 1 clinical trial during the third quarter of
2023.
General and administrative (G&A)
expenses totaled $2.5 million for the three months ended
September 30, 2023, compared to $2.8 million for the same period in
2022. The decrease in G&A expenses of $0.3 million was
primarily due to lower legal and professional fees.
Net loss for the three months
ended September 30, 2023, was $4.7 million, or $0.37 per share
basic and diluted, including non-cash stock-based compensation
expense of $0.8 million, compared to a net loss of $4.6 million, or
$0.38 per share basic and diluted, which included non-cash
stock-based compensation expense of $0.4 million for the three
months ended September 30, 2022.
Cash, cash equivalents and marketable
securities were $12.3 million as of September 30, 2023,
which the Company believes is sufficient to support operations into
the third quarter of 2024.
GAIN THERAPEUTICS, INC. |
CONDENSED CONSOLIDATED STATEMENTS OF
OPERATIONS |
|
(unaudited) |
|
|
Three Months Ended September 30, |
|
Nine Months Ended September 30, |
|
|
2023 |
|
2022 |
|
2023 |
|
2022 |
|
Revenues: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Collaboration revenues |
$ |
— |
|
|
$ |
— |
|
|
$ |
55,180 |
|
|
$ |
132,640 |
|
|
Other income |
|
— |
|
|
|
— |
|
|
|
— |
|
|
|
7,468 |
|
|
Total revenues |
$ |
— |
|
|
$ |
— |
|
|
$ |
55,180 |
|
|
$ |
140,108 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Operating expenses: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Research and development |
|
(2,367,482 |
) |
|
|
(1,964,784 |
) |
|
|
(9,146,630 |
) |
|
|
(6,103,448 |
) |
|
General and administrative |
|
(2,517,523 |
) |
|
|
(2,786,200 |
) |
|
|
(8,754,453 |
) |
|
|
(7,252,506 |
) |
|
Total operating expenses |
|
(4,885,005 |
) |
|
|
(4,750,984 |
) |
|
|
(17,901,083 |
) |
|
|
(13,355,954 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss from operations |
$ |
(4,885,005 |
) |
|
$ |
(4,750,984 |
) |
|
$ |
(17,845,903 |
) |
|
$ |
(13,215,846 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Other income/(expense): |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Interest income, net |
|
106,000 |
|
|
|
153,332 |
|
|
|
387,964 |
|
|
|
211,580 |
|
|
Foreign exchange gain/(loss), net |
|
82,198 |
|
|
|
43,491 |
|
|
|
(20,839 |
) |
|
|
102,865 |
|
|
Loss before income tax |
$ |
(4,696,807 |
) |
|
$ |
(4,554,161 |
) |
|
$ |
(17,478,778 |
) |
|
$ |
(12,901,401 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Income tax |
|
(21,456 |
) |
|
|
(4,048 |
) |
|
|
(64,773 |
) |
|
|
(14,871 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net loss |
$ |
(4,718,263 |
) |
|
$ |
(4,558,209 |
) |
|
$ |
(17,543,551 |
) |
|
$ |
(12,916,272 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net loss per shares: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net loss per share attributable to common stockholders - basic and
diluted |
$ |
(0.37 |
) |
|
$ |
(0.38 |
) |
|
$ |
(1.42 |
) |
|
$ |
(1.09 |
) |
|
Weighted average common shares - basic and diluted |
|
12,701,401 |
|
|
|
11,883,368 |
|
|
|
12,342,031 |
|
|
|
11,883,368 |
|
|
|
GAIN THERAPEUTICS, INC. |
CONDENSED CONSOLIDATED BALANCE SHEETS |
(unaudited) |
|
|
September 30,2023 |
|
December 31,2022 |
|
Assets |
|
|
|
|
|
|
|
|
Current assets: |
|
|
|
|
|
|
|
|
Cash and cash equivalents |
$ |
4,272,501 |
|
|
$ |
7,311,611 |
|
|
Marketable securities - current |
|
7,960,311 |
|
|
|
12,826,954 |
|
|
Tax credits |
|
101,911 |
|
|
|
103,877 |
|
|
Prepaid expenses and other current assets |
|
906,834 |
|
|
|
848,854 |
|
|
Total current assets |
$ |
13,241,557 |
|
|
$ |
21,091,296 |
|
|
|
|
|
|
|
|
|
|
|
Non-current assets: |
|
|
|
|
|
|
|
|
Marketable securities - non-current |
$ |
— |
|
|
$ |
1,941,488 |
|
|
Property and equipment, net |
|
127,393 |
|
|
|
144,379 |
|
|
Internal-use software |
|
189,242 |
|
|
|
213,967 |
|
|
Operating lease - right of use assets |
|
490,759 |
|
|
|
659,933 |
|
|
Restricted cash |
|
31,145 |
|
|
|
30,818 |
|
|
Long-term deposits and other non-current assets |
|
17,352 |
|
|
|
17,506 |
|
|
Total non-current assets |
|
855,891 |
|
|
|
3,008,091 |
|
|
Total assets |
$ |
14,097,448 |
|
|
$ |
24,099,387 |
|
|
|
|
|
|
|
|
|
|
|
Liabilities and stockholders' equity |
|
|
|
|
|
|
|
|
Current liabilities: |
|
|
|
|
|
|
|
|
Accounts payable |
$ |
1,376,859 |
|
|
$ |
1,626,100 |
|
|
Operating lease liability - current |
|
231,164 |
|
|
|
229,080 |
|
|
Other current liabilities |
|
2,692,587 |
|
|
|
2,106,756 |
|
|
Deferred income - current |
|
1,353,541 |
|
|
|
55,180 |
|
|
Loans - current |
|
109,281 |
|
|
|
108,135 |
|
|
Total current liabilities |
$ |
5,763,432 |
|
|
$ |
4,125,251 |
|
|
|
|
|
|
|
|
|
|
|
Non-current liabilities: |
|
|
|
|
|
|
|
|
Defined benefit pension plan |
$ |
160,512 |
|
|
$ |
157,580 |
|
|
Operating lease liability - non-current |
|
263,460 |
|
|
|
441,784 |
|
|
Deferred income - non-current |
|
144,339 |
|
|
|
— |
|
|
Loans - non-current |
|
434,938 |
|
|
|
495,258 |
|
|
Total non-current liabilities |
|
1,003,249 |
|
|
|
1,094,622 |
|
|
Total liabilities |
$ |
6,766,681 |
|
|
$ |
5,219,873 |
|
|
|
|
|
|
|
|
|
|
|
Stockholders’ equity |
|
|
|
|
|
|
|
|
Preferred stock, $0.0001 par value; 10,000,000 shares authorized;
nil shares issued and outstanding as of September 30, 2023 and
December 31, 2022. |
|
— |
|
|
|
— |
|
|
Common stock, $0.0001 par value: 50,000,000 shares authorized;
12,782,861 issued and outstanding as of September 30, 2023;
11,883,368 issued and outstanding as of December 31, 2022. |
|
1,278 |
|
|
|
1,189 |
|
|
Additional paid-in capital |
|
63,298,577 |
|
|
|
57,358,895 |
|
|
Accumulated other comprehensive income |
|
90,660 |
|
|
|
35,627 |
|
|
Accumulated deficit |
|
(38,516,197 |
) |
|
|
(20,925,459 |
) |
|
Loss for the period |
|
(17,543,551 |
) |
|
|
(17,590,738 |
) |
|
Total stockholders’ equity |
|
7,330,767 |
|
|
|
18,879,514 |
|
|
Total liabilities and stockholders’ equity |
$ |
14,097,448 |
|
|
$ |
24,099,387 |
|
|
|
About GT-02287Gain
Therapeutics’ lead drug candidate, GT-02287, is in development for
the treatment of GBA1 Parkinson’s disease (GBA1-PD). The orally
administered, brain-penetrant small molecule is an allosteric
protein modulator that restores the function of the lysosomal
protein enzyme glucocerebrosidase (GCase) which becomes misfolded
and impaired due to a GBA1 gene mutation, the most common genetic
abnormality associated with PD. In preclinical models of PD,
GT-02287 restored GCase enzymatic function, reduced aggregated
α-synuclein, neuroinflammation and neuronal death, increased
dopamine levels and improved motor function. Additionally, GT-02287
significantly reduced plasma neurofilament light chain (NfL)
levels, an emerging biomarker for neurodegeneration.
The program has been awarded funding support
from The Michael J. Fox Foundation for Parkinson’s Research (MJFF),
The Silverstein Foundation for Parkinson’s with GBA, and
InnoSuisse.
About GBA1 Parkinson’s
Disease
GBA1 Parkinson’s disease is caused by mutations
in the GBA1 gene, found in up to 15% of patients with Parkinson’s
disease and making it the primary genetic risk factor. The mutation
causes dysfunctional misfolding of the lysosomal enzyme
glucocerebrosidase (GCase), reducing its activity in the brain and
leading to the subsequent accumulation of α-synuclein and
neurodegeneration of dopamine cells. Patients with GBA1-PD tend to
have earlier onset and faster symptom progression than sporadic PD,
a progressive neurodegenerative disease characterized by a motor
syndrome consisting of bradykinesia (slowness of movement),
rigidity, resting tremors, and postural instability. With current
therapies treating only the symptoms of Parkinson’s disease without
affecting the underlying progression of the disease, there is an
unmet need to develop novel disease-modifying therapies such as
GT-02287 that have the potential to slow or stop disease
progression and help improve outcomes in this patient
population.
About Gain Therapeutics,
Inc.
Gain Therapeutics, Inc. is a clinical-stage
biotechnology company leading the discovery and development of next
generation allosteric therapies. Gain’s lead drug candidate
GT-02287, in development for the treatment of GBA1 Parkinson’s
disease, is currently being evaluated in a Phase 1 clinical
trial.
Leveraging AI-supported structural biology,
proprietary algorithms and supercomputer-powered physics-based
models, the company’s SEE-Tx® discovery platform can identify novel
allosteric binding sites on disease-implicated proteins,
pinpointing pockets that cannot be found or drugged with current
technologies. Gain’s unique approach enables the discovery of
novel, allosteric small molecule modulators that can restore or
disrupt protein function. Deploying its highly advanced platform,
Gain is accelerating drug discovery and unlocking novel
disease-modifying treatments for untreatable or difficult-to-treat
disorders including neurodegenerative diseases, rare genetic
disorders and oncology. For more information, please visit
GainTherapeutics.com and follow us on LinkedIn.
Cautionary Note Regarding
Forward-Looking Statements
This press release contains "forward-looking
statements" within the meaning of the Private Securities Litigation
Reform Act of 1995. All statements in this press release other than
statements of historical facts are “forward-looking statements”. In
some cases, you can identify these statements by forward-looking
words such as "may," "might," "will," "should," "expect," "plan,"
"anticipate," "believe," "estimate," "predict," "goal, " "intend,"
"seek, " "potential" or "continue," the negative of these terms and
variations of these words or similar expressions that are intended
to identify forward-looking statements, although not all
forward-looking statements contain these words. Forward-looking
statements in this press release include, but are not limited to,
statements regarding: the development of the Company’s current or
future product candidates including GT-02287; expectations
regarding the timing of results from a Phase 1 clinical study for
GT-02287; the potential therapeutic and clinical benefits of the
Company’s product candidates; the Company’s financial position and
ability to execute on the next phase of its strategy; and the
Company’s anticipated cash runway guidance, including the ability
for the Company’s current and projected cash to allow the Company
to meet value inflection points. These forward-looking statements
are based on the Company’s expectations and assumptions as of the
date of this press release. Each of these forward-looking
statements involves risks and uncertainties that could cause the
Company’s preclinical and future clinical development programs,
future results or performance to differ materially from those
expressed or implied by the forward-looking statements. These
statements are not historical facts but instead represent the
Company's belief regarding future results, many of which, by their
nature, are inherently uncertain and outside the Company's control.
Many factors may cause differences between current expectations and
actual results, including the impacts of the post-COVID-19
environment and other global and macroeconomic conditions on the
Company’s business; clinical trials and financial position;
unexpected safety or efficacy data observed during preclinical
studies or clinical trials, clinical trial site activation or
enrollment rates that are lower than expected; changes in expected
or existing competition; changes in the regulatory environment; the
uncertainties and timing of the regulatory approval process; and
unexpected litigation or other disputes. Other factors that may
cause the Company’s actual results to differ from those expressed
or implied in the forward-looking statements in this press release
are identified in the section titled “Risk Factors,” in the
Company’s Annual Report on Form 10-K filed with the Securities and
Exchange Commission on March 23, 2023 and its other documents
subsequently filed with or furnished to the Securities and Exchange
Commission from time to time. All forward-looking statements
contained in this press release speak only as of the date on which
they were made. The Company undertakes no obligation to update such
statements to reflect events that occur or circumstances that exist
after the date on which they were made, except as required by
law.
Investor & Media
Contact:
Susan SharpeLinnden Communications(919)
602-2330susan@linndencom.com
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