Scholar Rock's Optimistic Q2 Earnings Call: Apitegromab's Progress, Regulatory Milestones, and Commercial Launch Readiness.
PorAinvest
sábado, 9 de agosto de 2025, 4:35 pm ET1 min de lectura
ROCK--
The FDA has accepted the Biologics License Application (BLA) for apitegromab under priority review, setting a target action date of September 22, 2025. This regulatory milestone brings Scholar Rock one step closer to a potential U.S. commercial launch in 2025. The company is also advancing its Marketing Authorisation Application (MAA) in the EU, with a European launch anticipated in 2026.
Positive topline results from the Phase 2 EMBRAZE proof-of-concept trial in adult patients with obesity demonstrated statistically significant preservation of lean mass with apitegromab during tirzepatide-induced weight loss. This trial highlighted the broader potential of the company's highly selective myostatin inhibition approach.
The company reported a net loss of $110 million for the quarter ended June 30, 2025, compared to a net loss of $58.5 million for the same period in 2024. Research and development expenses increased to $62.4 million, up from $42.4 million in the prior year, primarily due to an increase in external research and development costs and employee-related expenses. General and administrative expenses also increased, driven by an increase in stock-based compensation and professional services fees.
Scholar Rock's cash, cash equivalents, and marketable securities totaled approximately $295 million as of June 30, 2025, providing a strong financial foundation to support commercial and development programs into 2027. The company will host an update call on August 6, 2025, at 8:00 a.m. ET to discuss its second-quarter 2025 results.
Challenges were noted, specifically observations at CDMO sites by the FDA that require attention. However, the company remains committed to addressing these issues and continuing its regulatory progress.
Scholar Rock's focus on developing innovative therapies for neuromuscular diseases and cardiometabolic disorders positions it as a leader in its field. The company's proprietary platform and selective monoclonal antibodies to modulate protein growth factors offer transformational potential in historically under-addressed disease spaces.
References:
[1] https://investors.scholarrock.com/news-releases/news-release-details/scholar-rock-reports-second-quarter-2025-financial-results-and
SRRK--
Scholar Rock's Q2 earnings call highlighted cautious optimism due to successful clinical trial results and strong regulatory progress for its lead product, apitegromab. The FDA has accepted the BLA for apitegromab under priority review, with a target action date set for September 22, 2025. The company is gearing up for a commercial launch in the U.S. and Europe, with a strong financial position expected to sustain operations into 2027. However, some challenges were noted, specifically observations at CDMO sites by the FDA that require attention.
Scholar Rock (NASDAQ: SRRK), a late-stage biopharmaceutical company, reported its second-quarter 2025 earnings, highlighting cautious optimism amidst successful clinical trial results and strong regulatory progress for its lead product, apitegromab. The company's financial position remains robust, with cash reserves expected to sustain operations into 2027.The FDA has accepted the Biologics License Application (BLA) for apitegromab under priority review, setting a target action date of September 22, 2025. This regulatory milestone brings Scholar Rock one step closer to a potential U.S. commercial launch in 2025. The company is also advancing its Marketing Authorisation Application (MAA) in the EU, with a European launch anticipated in 2026.
Positive topline results from the Phase 2 EMBRAZE proof-of-concept trial in adult patients with obesity demonstrated statistically significant preservation of lean mass with apitegromab during tirzepatide-induced weight loss. This trial highlighted the broader potential of the company's highly selective myostatin inhibition approach.
The company reported a net loss of $110 million for the quarter ended June 30, 2025, compared to a net loss of $58.5 million for the same period in 2024. Research and development expenses increased to $62.4 million, up from $42.4 million in the prior year, primarily due to an increase in external research and development costs and employee-related expenses. General and administrative expenses also increased, driven by an increase in stock-based compensation and professional services fees.
Scholar Rock's cash, cash equivalents, and marketable securities totaled approximately $295 million as of June 30, 2025, providing a strong financial foundation to support commercial and development programs into 2027. The company will host an update call on August 6, 2025, at 8:00 a.m. ET to discuss its second-quarter 2025 results.
Challenges were noted, specifically observations at CDMO sites by the FDA that require attention. However, the company remains committed to addressing these issues and continuing its regulatory progress.
Scholar Rock's focus on developing innovative therapies for neuromuscular diseases and cardiometabolic disorders positions it as a leader in its field. The company's proprietary platform and selective monoclonal antibodies to modulate protein growth factors offer transformational potential in historically under-addressed disease spaces.
References:
[1] https://investors.scholarrock.com/news-releases/news-release-details/scholar-rock-reports-second-quarter-2025-financial-results-and

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