
Metsera shares surged as much as 25% following positive early-stage trial results for its experimental weight-loss drug, MET-233i, which demonstrated an 8.4% placebo-adjusted weight loss at 36 weeks. The drug, an amylin mimetic with a 19-day half-life, supports potential once-a-month dosing, a possible advantage over weekly GLP-1 drugs like Lilly's Zepbound and Novo's Wegovy; the company is also exploring a combination therapy with its GLP-1 drug MET-097i, as drugmakers seek alternatives to GLP-1 based treatments.
Metsera (MTSR.O) shares experienced a significant intraday surge of up to 25% on Monday following the announcement of positive results from its 80-patient, early-stage trial for the experimental weight-loss drug, MET-233i. The study demonstrated that MET-233i led to a placebo-adjusted weight loss of 8.4% at 36 weeks. A key differentiating feature highlighted is the drug's half-life of approximately 19 days, which supports a potential once-a-month dosing regimen, contrasting favorably with the weekly administrations required for established GLP-1 drugs like Eli Lilly's Zepbound and Novo Nordisk's Wegovy. MET-233i is an amylin mimetic, a class of medicine mimicking a pancreatic hormone, and is being developed both as a standalone treatment and in combination with Metsera's own GLP-1 drug, MET-097i. This development positions Metsera, a company that went public in January, as a new contender in the lucrative obesity drug market, which is currently dominated by Novo Nordisk and Eli Lilly, and aligns with an industry trend of seeking next-generation treatments beyond GLP-1s that target other hormones or offer improved patient compliance. Notably, data for Novo Nordisk's own next-generation candidate, CagriSema, has previously fallen below investor expectations, while other companies like AstraZeneca are also exploring amylin-based therapies.
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