Structure Therapeutics (NASDAQ: GPCR) announced completion of enrollment for its aleniglipron obesity treatment studies ACCESS and ACCESS II, with topline data expected by year-end 2025. The studies, involving over 300 patients, will evaluate doses up to 240mg with optimized titration regiments.
The company reported strong financials with $883.5 million in cash and investments, expected to fund operations through 2027. R&D expenses increased to $108.8 million for 2024, up from $70.1 million in 2023. Net loss for 2024 was $122.5 million.
Structure Therapeutics is advancing its oral small molecule obesity portfolio, including ACCG-2671, an oral amylin receptor agonist expected to begin Phase 1 trials by year-end 2025. The company also maintains pipeline programs targeting GIPR, GCGR, and APJR for obesity treatment.
Structure Therapeutics' Q4 and full-year 2024 results reveal a company strategically positioned in the highly competitive obesity therapeutics market with two key differentiators: oral administration and a multi-modal approach targeting various metabolic pathways.
The completion of enrollment in both ACCESS studies for aleniglipron represents a significant operational achievement, particularly as the company describes it as the "second most advanced oral GLP-1 small molecule" in development. This positions Structure behind Pfizer's danuglipron but potentially ahead of other oral GLP-1 competitors. The anticipated 36-week data by year-end 2025 will be critical, as this duration approaches the timeframe needed to demonstrate meaningful efficacy and safety for obesity therapeutics, though full approval would typically require longer studies.
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