Sagimet Biosciences reported its Q3 2024 financial results, highlighting the Breakthrough Therapy designation from the FDA for denifanstat in MASH and the anticipated initiation of a Phase 3 program by the end of 2024. The company's cash runway is expected to last through 2025, with cash, cash equivalents, and marketable securities totaling $170.0 million as of September 30, 2024.
Denifanstat received Breakthrough Therapy designation from the FDA for MASH.
Phase 2b FASCINATE-2 study results of denifanstat were published in The Lancet Gastroenterology & Hepatology.
Sagimet completed end-of-Phase 2 interactions with the FDA on the development of denifanstat for MASH, with Phase 3 program initiation expected by the end of 2024.
The company anticipates a cash runway through 2025, with $170.0 million in cash, cash equivalents, and marketable securities as of September 30, 2024.
Sagimet Biosciences is focused on advancing denifanstat towards a pivotal Phase 3 program in MASH by the end of 2024.