Evoke Pharma Reports First Quarter 2025 Financial Results and Provides Business Update
Rhea-AI Summary
Evoke Pharma (NASDAQ: EVOK) reported strong Q1 2025 financial results, with net product sales increasing 77% year-over-year to $3.1 million. The company's performance was driven by significant growth in GIMOTI adoption, achieving a 73% increase in fill rate and 44% growth in total prescriber base compared to Q1 2024.
The company reported a net loss of $1.3 million ($0.51 per share), improved from $1.6 million loss in Q1 2024. Operating expenses increased to $4.4 million, up from $3.2 million in the same period last year. With $12.6 million in cash and cash equivalents, Evoke expects to fund operations into Q2 2026.
Evoke maintains its 2025 net product sales guidance of approximately $16 million, representing a 60% increase over 2024. The company also appointed Greg Pyszczymuka to its Board of Directors to strengthen commercial strategy.
Positive
- Net product sales grew 77% year-over-year to $3.1 million
- Fill rate increased 73% year-over-year
- Total prescriber base expanded by 44%
- Net loss improved to $1.3 million from $1.6 million year-over-year
- Strong cash position of $12.6 million, sufficient to fund operations into Q2 2026
- Maintained 2025 guidance of $16 million in net product sales
Negative
- Operating expenses increased 37.5% to $4.4 million
- Company still operating at a loss despite sales growth
- SG&A expenses increased to $4.3 million from $3.1 million
News Market Reaction 1 Alert
On the day this news was published, EVOK gained 0.32%, reflecting a mild positive market reaction.
Data tracked by StockTitan Argus on the day of publication.
Q1 2025 Net Product Sales Increased
Sustained Momentum Driven by Growing Prescriber Adoption and Repeat Patient Use
SOLANA BEACH, Calif., May 13, 2025 (GLOBE NEWSWIRE) -- Evoke Pharma, Inc. (NASDAQ: EVOK), a specialty pharmaceutical company focused on treatments for gastrointestinal (GI) disorders with an emphasis on GIMOTI®, today announced financial results for the first quarter ended March 31, 2025, and provided a business update.
“We’re pleased to report continued strong revenue growth in the first quarter of 2025,” said Matt D’Onofrio, Chief Executive Officer of Evoke Pharma, Inc. “Net product sales rose
First Quarter 2025 Highlights and Recent Developments
Corporate Governance
- Appointed Greg Pyszczymuka to the Board of Directors. His extensive experience in commercial strategy and revenue growth will be valuable as the company advances its market position.
Commercial Execution
- GIMOTI demonstrated solid momentum in Q1 with strong repeat usage, increasing prescription depth, and stable conversion rates.
- Realized a
73% year-over-year increase in fill rate, driven by expanded pharmacy partnerships and reduced fulfillment friction. - Grew the total prescriber base by
44% , with increased provider confidence in GIMOTI’s efficacy and convenience. - Maintained strategic emphasis on GLP-1 patient populations, where the need for effective non-oral options continues to grow.
First Quarter 2025 Financial Results
For the first quarter of 2025, net product sales were approximately
For the first quarter of 2025, selling, general, and administrative expenses were approximately
Total operating expenses for the first quarter of 2025 were approximately
As of March 31, 2025, cash and cash equivalents were approximately
2025 Outlook
Evoke reiterates its 2025 net product sales guidance of approximately
“We’ve entered 2025 with strong momentum and a clear path forward,” added Mr. D’Onofrio. “With focused execution, expanded provider engagement, and the ongoing relevance of GIMOTI in a growing diabetic patient population, we’re confident in our ability to continue delivering growth and impact for patients who need better treatment options.”
About Evoke Pharma, Inc.
Evoke is a specialty pharmaceutical company focused primarily on the development of drugs to treat GI disorders and diseases. We developed, commercialized and markets GIMOTI, a nasal spray formulation of metoclopramide, for the relief of symptoms associated with acute and recurrent diabetic gastroparesis in adults.
Diabetic gastroparesis is a GI disorder affecting millions of patients worldwide, in which the stomach takes too long to empty its contents resulting in serious GI symptoms as well as other systemic complications. The gastric delay caused by gastroparesis can compromise absorption of orally administered medications. Prior to FDA approval to commercially market GIMOTI, metoclopramide was only available in oral and injectable formulations and remains the only drug currently approved in the United States to treat gastroparesis.
Visit www.EvokePharma.com for more information.
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About Gimoti® (metoclopramide) nasal spray
GIMOTI is indicated for the relief of symptoms in adults with acute and recurrent diabetic gastroparesis. Important Safety Information
WARNING: TARDIVE DYSKINESIA
- Metoclopramide can cause tardive dyskinesia (TD), a serious movement disorder that is often irreversible. The risk of developing TD increases with duration of treatment and total cumulative dosage.
- Discontinue GIMOTI in patients who develop signs or symptoms of TD. In some patients, symptoms may lessen or resolve after metoclopramide is stopped.
- Avoid treatment with metoclopramide (all dosage forms and routes of administration) for longer than 12 weeks because of the increased risk of developing TD with longer-term use.
GIMOTI is not recommended for use in:
- Pediatric patients due to the risk of developing tardive dyskinesia (TD) and other extrapyramidal symptoms as well as the risk of methemoglobinemia in neonates.
- Moderate or severe hepatic impairment (Child-Pugh B or C), moderate or severe renal impairment (creatinine clearance less than 60 mL/minute), and patients concurrently using strong CYP2D6 inhibitors due to the risk of increased drug exposure and adverse reactions.
GIMOTI is contraindicated:
- In patients with a history of tardive dyskinesia (TD) or a dystonic reaction to metoclopramide.
- When stimulation of gastrointestinal motility might be dangerous (e.g., in the presence of gastrointestinal hemorrhage mechanical obstruction, or perforation).
- In patients with pheochromocytoma or other catecholamine-releasing paragangliomas. Metoclopramide may cause a hypertensive/pheochromocytoma crisis, probably due to release of catecholamines from the tumor.
- In patients with epilepsy. Metoclopramide may increase the frequency and severity of seizures.
- In patients with hypersensitivity to metoclopramide. Reactions have included laryngeal and glossal angioedema and bronchospasm.
Potential adverse reactions associated with metoclopramide include: Tardive dyskinesia (TD), other extrapyramidal effects (EPS), parkinsonism symptoms, motor restlessness, neuroleptic malignant syndrome (NMS), depression, suicidal ideation and suicide, hypertension, fluid retention, hyperprolactinemia, effects on the ability to drive and operate machinery. Most common adverse reactions (≥
Visit www.fda.gov/medwatch or call 1-800-FDA-1088.
Safe Harbor Statement
Evoke cautions you that statements included in this press release that are not a description of historical facts are forward-looking statements. In some cases, you can identify forward-looking statements by terms such as “may,” “will,” “should,” “expect,” “plan,” “anticipate,” “could,” “intend,” “target,” “project,” “contemplates,” “believes,” “estimates,” “predicts,” “potential” or “continue” or the negatives of these terms or other similar expressions.
These statements are based on the company’s current beliefs and expectations. These forward-looking statements include statements regarding: guidance regarding 2025 net product sales; potential future provider engagement; the ongoing relevance of GIMOTI in a growing diabetic population; Evoke’s commercialization plans, including underlying drivers of potential growth and seasonality in sales; and Evoke’s expected cash runway. The inclusion of forward-looking statements should not be regarded as a representation by Evoke that any of its plans will be achieved. Actual results may differ from those set forth in this press release due to the risks and uncertainties inherent in Evoke’s business, including, without limitation: Evoke may not be able to achieve its guidance for 2025 including as a result of decreased demand for GIMOTI; Evoke’s and EVERSANA’s ability to successfully drive market demand for GIMOTI; Evoke’s ability to obtain additional financing as needed to support its operations; Evoke may use its capital resources sooner than expected; EVERSANA may terminate the commercial services agreement and loan agreement which would require us to repay the outstanding principal and interest underlying our loan agreement with EVERSANA; Evoke’s dependence on third parties for the manufacture of GIMOTI; Evoke is entirely dependent on the success of GIMOTI; inadequate efficacy or unexpected adverse side effects relating to GIMOTI that could result in recalls or product liability claims; Evoke’s ability to maintain intellectual property protection for GIMOTI; and other risks and uncertainties detailed in Evoke’s prior press releases and in the periodic reports it files with the Securities and Exchange Commission. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof, and Evoke undertakes no obligation to revise or update this press release to reflect events or circumstances after the date hereof. All forward-looking statements are qualified in their entirety by this cautionary statement. This caution is made under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.
Investor & Media Contact:
Daniel Kontoh-Boateng
DKB Partners
Tel: 862-213-1398
dboateng@dkbpartners.net
| Evoke Pharma, Inc. | |||||||
| Balance Sheets | |||||||
| March 31, | December 31, | ||||||
| 2025 | 2024 | ||||||
| (Unaudited) | |||||||
| Assets | |||||||
| Current assets: | |||||||
| Cash and cash equivalents | $ | 12,624,090 | $ | 13,596,600 | |||
| Accounts receivable, net of allowance for credit losses of | 2,511,490 | 2,420,373 | |||||
| Prepaid expenses | 523,910 | 731,945 | |||||
| Inventories | 532,145 | 445,081 | |||||
| Other current assets | 39,240 | 43,898 | |||||
| Total current assets | 16,230,875 | 17,237,897 | |||||
| Operating lease right-of-use asset | 138,758 | 154,184 | |||||
| Deferred offering costs | — | 120,614 | |||||
| Other long-term assets | 6,312 | 6,312 | |||||
| Total assets | $ | 16,375,945 | $ | 17,519,007 | |||
| Liabilities and stockholdersʼ equity | |||||||
| Current liabilities: | |||||||
| Accounts payable and accrued expenses | $ | 2,781,203 | $ | 2,341,191 | |||
| Accrued compensation | 371,732 | 865,650 | |||||
| Operating lease liability | 61,625 | 59,533 | |||||
| Note payable | 5,000,000 | 5,000,000 | |||||
| Accrued interest payable | 2,236,953 | 2,113,665 | |||||
| Total current liabilities | 10,451,513 | 10,380,039 | |||||
| Operating lease liability, net of current portion | 83,217 | 100,958 | |||||
| Total liabilities | 10,534,730 | 10,480,997 | |||||
| Commitments and contingencies | |||||||
| Stockholdersʼ equity: | |||||||
| Preferred stock, | — | — | |||||
| Common stock, | 149 | 149 | |||||
| Additional paid-in capital | 135,938,876 | 135,829,493 | |||||
| Accumulated deficit | (130,097,810 | ) | (128,791,632 | ) | |||
| Total stockholdersʼ equity | 5,841,215 | 7,038,010 | |||||
| Total liabilities and stockholdersʼ equity | $ | 16,375,945 | $ | 17,519,007 | |||
| Evoke Pharma, Inc. | |||||||
| Statements of Operations | |||||||
| Three Months Ended March 31, | |||||||
| 2025 | 2024 | ||||||
| Net product sales | $ | 3,080,158 | $ | 1,735,490 | |||
| Operating expenses: | |||||||
| Cost of goods sold | 41,613 | 92,529 | |||||
| Research and development | 42,783 | 4,645 | |||||
| Selling, general and administrative | 4,297,505 | 3,139,536 | |||||
| Total operating expenses | 4,381,901 | 3,236,710 | |||||
| Loss from operations | (1,301,743 | ) | (1,501,220 | ) | |||
| Other income (expense): | |||||||
| Interest income | 118,853 | 46,058 | |||||
| Interest expense | (123,288 | ) | (124,658 | ) | |||
| Total other expense | (4,435 | ) | (78,600 | ) | |||
| Net loss | $ | (1,306,178 | ) | $ | (1,579,820 | ) | |
| Net loss per share of common stock, basic and diluted | $ | (0.51 | ) | $ | (2.09 | ) | |
| Weighted-average shares used to compute basic and diluted net loss per share | 2,548,684 | 756,808 | |||||