Gemini Therapeutics Completes 60 Patients Enrollment In Lead Candidate Mid-Stage Study In Dry AMD

by Vandana Singh, Benzinga Editor
February 10, 2021 12:07 PM | 1 min read |
  • Gemini Therapeutics Inc (NASDAQ: GMTX) concludes enrollment in its Phase 2a ReGAtta study evaluating GEM103, a recombinant human complement factor H (CFH), in dry Age-related macular degeneration (AMD) patients with CFH loss-of-function gene variants.
  • The 60-subject trial is designed to evaluate safety and tolerability and measures of intraocular pharmacokinetics (PK) and disease-relevant biomarkers. Topline data anticipated in the first half of 2021.
  • The FDA granted Fast Track Designation for GEM103 to treat dry AMD in patients with CFH loss of function gene variants.
  • Price Action: GMTX shares moved 2.95% higher at 13.27 during market hours on the last check Wednesday.
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BiotechNewsFDAGeneralAge-Related Macular DegenerationPhase 2A Trial
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