A Phase 1, Multicenter, Open-label, Single-dose, Dose-escalation Study in Patients With Geographic Atrophy (GA) Secondary to Dry Age-related Macular Degeneration (AMD) to Evaluate the Safety, Tolerability, Pharmacodynamics, and Immunogenicity of Intravitreal Injections of GEM103
Latest Information Update: 15 Feb 2021
At a glance
- Drugs Recombinant complement factor H Gemini Therapeutics (Primary)
- Indications Dry age-related macular degeneration
- Focus Adverse reactions; First in man
- Sponsors Gemini Therapeutics
Most Recent Events
- 09 Feb 2021 Status changed from active, no longer recruiting to completed.
- 13 Nov 2020 Results presented in a Gemini Therapeutics media release.
- 08 Oct 2020 Planned End Date changed from 1 Sep 2020 to 1 Dec 2020.