Structure Therapeutics Reports First Quarter 2025 Financial Results and Recent Highlights
- Strong cash position of $836.9M, sufficient to fund operations through 2027
- Two Phase 2b trials for aleniglipron fully enrolled with data expected by end-2025
- Development of multiple oral small molecule programs targeting obesity (GLP-1R, GIPR, GCGR, APJR)
- ANPA-0073 showed good tolerability in Phase 1 trials with no serious adverse events
- Increased net loss of $46.8M in Q1 2025 compared to $26.0M in Q1 2024
- R&D expenses more than doubled to $42.9M from $20.7M year-over-year
- Current cash position excludes funding for Phase 3 registrational studies
Insights
Structure Therapeutics advancing oral GLP-1 and amylin programs on schedule with strong cash position despite increased R&D burn.
Structure Therapeutics is methodically advancing its oral small molecule approach for metabolic diseases, particularly obesity. Their lead candidate aleniglipron has reached a critical milestone with fully enrolled Phase 2b studies (ACCESS and ACCESS II), evaluating doses up to 240 mg with data expected by year-end 2025. This represents a significant inflection point that will determine whether the program advances to pivotal trials.
Their second asset, ACCG-2671, an oral small molecule amylin receptor agonist, is progressing toward Phase 1 initiation by year-end. The company positions this as potentially the most advanced oral amylin program in development. New preclinical data will be presented at the ADA Scientific Sessions in June, which should provide insights into its metabolic effects.
Structure is building a comprehensive platform approach with additional programs targeting diverse metabolic pathways (GIPR, GCGR, and APJR). Notably, their APJR agonist ANPA-0073 is already Phase 2-ready after completing Phase 1 with favorable tolerability. The company is also exploring GLP-1R applications beyond obesity, including Parkinson's disease.
The strategic focus on oral small molecules addresses a clear market need for more convenient administration compared to injectable GLP-1s, though efficacy and safety relative to established products will ultimately determine commercial potential. The company's multi-mechanism approach provides pipeline diversification that partially mitigates inherent development risks.
Structure Therapeutics maintains a robust financial position with
The company's quarterly financials reveal accelerating investment in their pipeline. R&D expenses more than doubled year-over-year to
Their current burn rate approximates
The explicit exclusion of Phase 3 costs from the runway forecast is noteworthy. Late-stage clinical trials typically require substantially greater investment than earlier phases. Should aleniglipron advance to pivotal studies, additional financing strategies would likely be required despite the current strong position.
Overall, Structure's financial foundation remains solid with sufficient resources to reach multiple key milestones. The increased R&D investment, while widening near-term losses, reflects appropriate capital allocation toward advancing their promising pipeline assets on schedule.
Topline data from oral small molecule aleniglipron (GSBR-1290) Phase 2b ACCESS and ACCESS II studies anticipated by year-end 2025
Oral small molecule amylin receptor agonist (ACCG-2671) Phase 1 initiation anticipated by year-end 2025; New preclinical data to be presented at American Diabetes Association (ADA) 85th Scientific Sessions in June 2025
Strong financial position with cash,
cash equivalents and short-term investments of
SAN FRANCISCO, May 08, 2025 (GLOBE NEWSWIRE) -- Structure Therapeutics Inc. (NASDAQ: GPCR), a clinical-stage global biopharmaceutical company developing novel oral small molecule therapeutics for metabolic diseases, including obesity, today reported financial results for the first quarter ended March 31, 2025, and provided a business update.
“We are excited by the recent advancements in the oral small molecule GLP-1 field, which will meaningfully expand access and options for patients with obesity and related diseases,” said Raymond Stevens, Ph.D., CEO of Structure Therapeutics. “We continue to make strong progress with the Phase 2b ACCESS and ACCESS II studies for aleniglipron, our once-daily oral small molecule GLP-1 program, which are on track for data readout by the end of the year. In addition, we are on track to initiate the Phase 1 study of ACCG-2671, which we believe is the most advanced oral small molecule amylin program in development, by the end of 2025. We’re advancing our powerful foundation for the future of fixed-dose combination therapies which is best addressed with oral small molecules and to make these medicines more broadly accessible and convenient to patients.”
Recent and Upcoming Milestones
Aleniglipron (GSBR-1290) – Oral Small Molecule Selective GLP-1 Receptor Agonist for the Treatment of Obesity or Overweight with Co-Morbidities
- The Phase 2b ACCESS and ACCESS II studies are fully enrolled and on track for topline 36-week data by year-end 2025.
- ACCESS enrolled approximately 220 adults living with obesity, or overweight with a weight-related comorbidity, and is designed to evaluate doses up to 120 mg of aleniglipron with a 4-week titration regimen.
- ACCESS II enrolled approximately 80 adults living with obesity, or overweight with a weight-related comorbidity, and is designed to evaluate higher doses of aleniglipron (180 mg and 240 mg) with 4-week titration increments.
ACCG-2671 – Oral Small Molecule Amylin Receptor Agonist for the Treatment of Obesity or Overweight with Co-Morbidities
- Investigational new drug (IND) enabling activities for ACCG-2671 are ongoing; Structure Therapeutics plans to initiate a first-in-human Phase 1 clinical study by year-end 2025.
- New preclinical data for ACCG-2671 will be presented in a late-breaking poster session at the American Diabetes Association (ADA) 85th Scientific Sessions on June 22, 2025.
Oral Small Molecule Pipeline and Potential Combinations:
- Oral Small Molecule GLP-1R in additional indications: Structure Therapeutics is studying GLP-1 receptor agonists in additional indications outside of obesity, including Parkinson’s disease (PD). Preclinical data in PD will be presented in a late-breaking poster session at the ADA 85th Scientific Sessions on June 22, 2025.
- Oral Small Molecule GIPR Program: Structure Therapeutics is developing a GIPR selective agonist and antagonist and GLP-1R/GIPR combinations to treat obesity and associated diseases.
- Oral Small Molecule GCGR Program: Structure Therapeutics is developing a GCGR selective agonist and GLP-1R/GCGR combinations for the treatment of obesity and related diseases.
- Oral Small Molecule APJR Program: Structure Therapeutics is evaluating ANPA-0073, a Phase 2 ready biased APJR agonist for potential selective or muscle-sparing weight loss. The Company has completed a Phase 1 single-ascending and multiple-ascending dose study, in which ANPA-0073 was generally well-tolerated with no serious adverse events reported. Long term chronic GLP-toxicology studies are currently underway and expected to be completed in 2025.
First Quarter 2025 Financial Highlights
Cash Position: Cash, cash equivalents and short-term investments totaled
Research and Development (R&D) Expenses: R&D expenses for the first quarter of 2025 were
General and Administrative (G&A) Expenses: G&A expenses for the first quarter of 2025 were
Net Loss: Net loss for the first quarter of 2025 totaled
About Structure Therapeutics
Structure Therapeutics is a science-driven clinical-stage biopharmaceutical company focused on discovering and developing innovative oral small molecule treatments for chronic metabolic and cardiopulmonary conditions with significant unmet medical needs. Utilizing its next generation structure-based drug discovery platform, the Company has established a robust GPCR-targeted pipeline, featuring multiple wholly-owned proprietary clinical-stage oral small molecule compounds designed to surpass the scalability limitations of traditional biologic and peptide therapies and be accessible to more patients around the world. For additional information, please visit www.structuretx.com.
Forward Looking Statements
This press release contains “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. All statements other than statements of historical fact are statements that could be deemed forward-looking statements, including, without limitation, statements concerning: the Company’s future plans and prospects; the expected timing of topline data from the ACCESS and ACCESS II studies; the planned initiation of the ACCG-2671 Phase 1 study and the timing thereof; the expected completion of long term chronic GLP-toxicology studies; the Company’s anticipated cash runway and uses of cash; the belief that the oral small molecule approach gives Structure Therapeutics the opportunity to create more scalable, cost-effective treatments to meet the needs of patients with obesity and other related diseases, without compromising on efficacy or safety; the belief that Structure Therapeutics is well-positioned with one of the most robust oral small molecule metabolic franchises in the industry; and any expectations regarding the safety, efficacy or tolerability of aleniglipron, ACCG-2671, ANPA-0073 and other candidates under development. In addition, when or if used in this press release, the words and phrases “anticipated,” “expect,” “on track,” “plan,” “potential,” “to be,” and similar expressions and their variants, as they relate to the Company may identify forward-looking statements. Forward-looking statements are neither historical facts nor assurances of future performance. Although the Company believes the expectations reflected in such forward-looking statements are reasonable, the Company can give no assurance that such expectations will prove to be correct. Readers are cautioned that actual results, levels of activity, safety, performance or events and circumstances could differ materially from those expressed or implied in the Company’s forward-looking statements due to a variety of risks and uncertainties, which include, without limitation, risks and uncertainties related to the results from earlier clinical studies not necessarily being predictive of future results, potential delays in the commencement, enrollment and completion of the Company’s planned clinical studies, the Company’s ability to advance aleniglipron, ACCG-2671, ANPA-0073, LTSE-2578, and its other therapeutic candidates, obtain regulatory approval of and ultimately commercialize the Company’s therapeutic candidates, competitive products or approaches limiting the commercial value of the Company’s product candidates, the timing and results of preclinical and clinical studies, the Company’s ability to fund development activities and achieve development goals, the Company's reliance on third parties, including clinical research organizations, manufacturers, suppliers and collaborators, over which it may not always have full control, the impact of any global pandemics, inflation, tariffs, changes in monetary and fiscal policy, supply chain issues, rising interest rates, future bank failures and other macroeconomic factors on the Company’s business, its ability to protect its intellectual property and other risks and uncertainties described in the Company’s filings with the Securities and Exchange Commission (SEC), including the Company’s latest Annual Report on Form 10-K and future reports the Company may file with the SEC from time to time. All forward-looking statements contained in this press release speak only as of the date on which they were made and are based on management’s assumptions and estimates as of such date. 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.
| STRUCTURE THERAPEUTICS INC. Condensed Consolidated Statements of Operations (unaudited) (In thousands) | ||||||||
| THREE MONTHS ENDED | ||||||||
| MARCH 31, | ||||||||
| 2025 | 2024 | |||||||
| Operating expenses: | ||||||||
| Research and development | $ | 42,867 | $ | 20,679 | ||||
| General and administrative | 13,444 | 11,336 | ||||||
| Total operating expenses | 56,311 | 32,015 | ||||||
| Loss from operations | (56,311 | ) | (32,015 | ) | ||||
| Interest and other income, net | 9,576 | 6,008 | ||||||
| Loss before provision for income taxes | (46,735 | ) | (26,007 | ) | ||||
| Provision for (benefit from) income taxes | 98 | 29 | ||||||
| Net loss | $ | (46,833 | ) | $ | (26,036 | ) | ||
| STRUCTURE THERAPEUTICS INC. Condensed Consolidated Balance Sheet Data (unaudited) (In thousands) | ||||||||
| MARCH 31, | DECEMBER 31, | |||||||
| 2025 | 2024 | |||||||
| Assets | ||||||||
| Current assets: | ||||||||
| Cash, cash equivalents and short-term investments | $ | 836,882 | $ | 883,518 | ||||
| Prepaid expenses and other current assets | 12,740 | 7,693 | ||||||
| Total current assets | 849,622 | 891,211 | ||||||
| Property and equipment, net | 3,518 | 3,478 | ||||||
| Operating right-of-use assets | 7,313 | 3,535 | ||||||
| Other non-current assets | 6,096 | 5,106 | ||||||
| Total assets | $ | 866,549 | $ | 903,330 | ||||
| Liabilities and shareholders’ equity | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 8,710 | $ | 8,024 | ||||
| Accrued expenses and other current liabilities | 25,306 | 26,299 | ||||||
| Operating lease liabilities, current portion | 2,471 | 1,698 | ||||||
| Total current liabilities | 36,487 | 36,021 | ||||||
| Operating lease liabilities, net of current portion | 5,116 | 2,164 | ||||||
| Other non-current liabilities | 308 | 302 | ||||||
| Total liabilities | 41,911 | 38,487 | ||||||
| Total shareholders’ equity | 824,638 | 864,843 | ||||||
| Total liabilities and shareholders’ equity | $ | 866,549 | $ | 903,330 | ||||
Investors:
Danielle Keatley
Structure Therapeutics Inc.
ir@structuretx.com
Media:
Dan Budwick
1AB
Dan@1abmedia.com
FAQ
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