Key Performance
More- Earnings Score: N/A
- Momentum Score: 38
- True Yield: N/A
- Financial Health Score: N/A
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Latest Research & News
Over 50 pharmaceutical companies are advancing 55+ pipeline hemophilia drugs across various clinical development stages. Key players including Novo Nordisk, Roche, Regeneron, and others are developing innovative therapies with mechanisms like FVIII mimetics, gene therapies, and factor replacement treatments. Recent developments include Novo Nordisk's FDA submission for denecimig and Metagenomi's progress toward clinical trials for gene-editing therapy MGX-001.
05/05/2026, 1:00 PM • GlobeNewswire
Metagenomi Therapeutics announced a publication in Nature Structural & Molecular Biology highlighting MG119-28, a compact CRISPR nuclease demonstrating superior editing efficiency compared to previous compact nucleases. The nuclease showed 64% knockdown of target protein in mice via single AAV injection, supporting the company's path toward clinically relevant genome editing systems deliverable via AAV for non-hepatic indications including neuromuscular diseases.
04/16/2026, 7:00 AM • GlobeNewswire
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Company Profile
Metagenomi Therapeutics, Inc. an in vivo genome editing company, develops curative genetic medicines in the United States. The company's lead development program, MGX-001, is designed to provide curative, life-long protection from bleeding events and joint damage in adults and children with hemophilia. It has a collaboration agreement with Ionis Pharmaceuticals, Inc. for apolipoprotein C-III for the treatment of hyper triglyceridemia, transthyretin (TTR) for transthyretin amyloidosis, angiotensinogen (AGT) for refractory hypertension, and other programs. The company was formerly known as Metagenomi, Inc. and changed its name to Metagenomi Therapeutics, Inc. in January 2026. Metagenomi Therapeutics, Inc. was incorporated in 2016 and is headquartered in Emeryville, California.