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NCT06541704 · ClinicalTrials.gov registry record · Phase 3
A Study Investigating Subcutaneously Administered Pozelimab in Combination With Cemdisiran or Cemdisiran Alone in Adult Participants With Geographic Atrophy
A Phase 3 study of Age-related Macular Degeneration (AMD) and Geographic Atrophy (GA), sponsored by Regeneron Pharmaceuticals.
- Recruiting
- Registry status
- Phase 3
- Development phase
- 975
- Enrollment target
- 20
- Study locations
NCT06541704: Recruiting Phase 3 study of Age-related Macular Degeneration (AMD) and Geographic Atrophy (GA), sponsored by Regeneron Pharmaceuticals.
NCT06541704 is a Phase 3 study of Age-related Macular Degeneration (AMD) and Geographic Atrophy (GA) that is actively recruiting participants, run by Regeneron Pharmaceuticals. The registered enrollment target is 975 participants, below the 101,783-participant average among 7 other Age-related Macular Degeneration (AMD) trials with a reported enrollment target (99% lower). The trial reports 20 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06541704, a Phase 3 study of Age-related Macular Degeneration (AMD) and Geographic Atrophy (GA), is actively recruiting participants, sponsored by Regeneron Pharmaceuticals.
- RECRUITING
- Registry status
- Phase 3
- Development phase
- 975 participants
- Enrollment target
- 20
- Study locations
Study Summary
This study is researching experimental (study) drugs called pozelimab and cemdisiran. The study is focused on participants who have Geographic Atrophy (GA) caused by Age-related Macular Degeneration (AMD). Geographic atrophy is a medical term that refers to later-stage cases of AMD which is an eye condition affecting central vision (what one sees straight ahead). The purpose of this study is to evaluate the progression rate of Geographic Atrophy in eyes of patients treated with cemdisiran alone or in combination with pozelimab compared to those treated with placebo. The study is looking at several other research questions, including: * What side effects may happen from taking the study drug(s) * How much study drug(s) are in the blood at different times * Whether the body makes antibodies against the study drug(s) (which could make the study drug(s) less effective or could lead to side effects)
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Pozelimab
- DRUG Cemdisiran
Study Locations (20)
California
- Retina Vitreous Associates Medical Group - Beverly Hills
- Retina Specialists of Beverly Hills- Department of Ophthalmology - Beverly Hills
- The Retina Partners - Encino
- Eye Medical Center of Fresno - Fresno
- Retina Consultants of Orange County - Fullerton
- Salehi Retina Institute dba Retina Associates of Southern California - Huntington Beach
- University of California Irvine - Irvine
- University of California San Diego, Jacobs Retina Center - La Jolla
- South Coast Retina Center - Long Beach
- American Institute of Research - Los Angeles
- Kaiser Permanente Los Angeles Medical Center - Los Angeles
- Retinal Consultants Medical Group Inc Modesto - Modesto
- Northern California Retina Vitreous Associates Medical Group, Inc. - Mountain View
Arizona
- Barnet Dulaney Perkins Eye Center-Ophthamalogy - Chandler
- Barnet Dulaney Perkins Eye Center - Phoenix
- Associated Retina Consultants - Phoenix
- Retinal Research Institute - Phoenix
- Retina Macula Institute of Arizona - Scottsdale
- Retina Associates of Tuscan - Tucson
Arkansas
- Retina Partners of Northwest Arkansas, PLLC - Springdale
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 975 participants |
| Start Date | 2024-10-30 |
| Est. Completion | 2032-05-21 |
| Phase | Phase 3 |
What NCT06541704 shows while recruiting
NCT06541704 is an interventional study that assigns participants to a tested intervention. The registered 975 participants enrollment target is mid-sized for trials with a published cap, below the 101,783-participant average among 7 other Age-related Macular Degeneration (AMD) trials with a reported enrollment target (99% lower).
The record links to 2 conditions, with Age-related Macular Degeneration (AMD) appearing as the primary indexed condition, and to 3 interventions - of which Placebo is the first listed.
NCT06541704 names 20 study sites across 3 states, led by California, Arizona, Arkansas.
Frequently Asked Questions
What is clinical trial NCT06541704 about?
NCT06541704 is a clinical study titled "A Study Investigating Subcutaneously Administered Pozelimab in Combination With Cemdisiran or Cemdisiran Alone in Adult Participants With Geographic Atrophy". This study is researching experimental (study) drugs called pozelimab and cemdisiran. The study is focused on participants who have Geographic Atrophy (GA) caused by Age-related Macular Degeneration (AMD). Geographic atrophy is a medical term that refers to later-stage cases of AMD which is an eye c...
What is the current status of trial NCT06541704?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 975 participants. The study started on 2024-10-30. Estimated completion is 2032-05-21.
What conditions does trial NCT06541704 study?
This clinical trial studies the following conditions: Age-related Macular Degeneration (AMD), Geographic Atrophy (GA).
What interventions are being tested in trial NCT06541704?
The interventions under investigation include: Placebo (DRUG), Pozelimab (DRUG), Cemdisiran (DRUG).
Who is sponsoring clinical trial NCT06541704?
This trial is sponsored by Regeneron Pharmaceuticals, which has 280 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06541704 being conducted?
This trial has 20 study locations across Arizona, Arkansas, California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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