RecruitingPhase 2NCT07215390
A Phase 2, Randomized, Placebo Controlled, Multicenter, Masked Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacodynamics of Multidose APL 3007 in Combination With Syfovre/Pegcetacoplan (APL-2) in Patients Diagnosed With Geographic Atrophy Secondary to Age Related Macular Degeneratio
Studying Medullary sponge kidney
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Apellis Pharmaceuticals, Inc.
- Intervention
- APL-3007, pegcetacoplan (APL-2)(drug)
- Enrollment
- 240 target
- Eligibility
- 60 years · All sexes
- Timeline
- 2025 – 2027
Study locations (30)
- Barnet Dulaney Perkins Eye Center (01018), Mesa, Arizona, United States
- Associated Retina Consultants - Phoenix, Phoenix, Arizona, United States
- Retinal Research Institute, LLC (01021), Phoenix, Arizona, United States
- California Retina Consultants (CRC) - Bakersfield Office, Bakersfield, California, United States
- The Retina Partners - Encino, Encino, California, United States
- Retina Consultants of Orange County - Fullerton Office, Fullerton, California, United States
- Salehi Retina Institute, Inc dba Retina Associate or Southern California (01034), Huntington Beach, California, United States
- Retina Consultants San Diego, Poway, California, United States
- Orange County Retina Medical Group, Santa Ana, California, United States
- Bay Area Retina Associates - Walnut Creek, Walnut Creek, California, United States
- Colorado Retina Associates, PLLC, Lakewood, Colorado, United States
- Advanced Vision Research Institute, Longmont, Colorado, United States
- Florida Retina Institute - Orlando (01053), Orlando, Florida, United States
- Retina Specialty Institute - Pensacola, Pensacola, Florida, United States
- Retina Vitreous Associates of Florida (RVA) - Saint Petersburg, St. Petersburg, Florida, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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