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NCT07215390 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study of Geographic Atrophy Secondary to Age-related Macular Degeneration, sponsored by Apellis Pharmaceuticals.

Recruiting
Registry status
Phase 2
Development phase
240
Enrollment target
20
Study locations

NCT07215390: Recruiting Phase 2 study of Geographic Atrophy Secondary to Age-related Macular Degeneration, sponsored by Apellis Pharmaceuticals.

NCT07215390 is a Phase 2 study of Geographic Atrophy Secondary to Age-related Macular Degeneration that is actively recruiting participants, run by Apellis Pharmaceuticals. The registered enrollment target is 240 participants, above the 166-participant average among 4 other Geographic Atrophy Secondary to Age-related Macular Degeneration trials with a reported enrollment target (45% higher). The trial reports 20 study locations across 11 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07215390, a Phase 2 study of Geographic Atrophy Secondary to Age-related Macular Degeneration, is actively recruiting participants, sponsored by Apellis Pharmaceuticals.

RECRUITING
Registry status
Phase 2
Development phase
240 participants
Enrollment target
20
Study locations

Study Summary

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 Degeneration

Interventions

  • DRUG APL-3007, pegcetacoplan (APL-2)
  • OTHER Placebo, Syfovre

Study Locations (20)

California

  • California Retina Consultants (CRC) - Bakersfield Office - Bakersfield
  • The Retina Partners - Encino - Encino
  • Retina Consultants of Orange County - Fullerton Office - Fullerton
  • Salehi Retina Institute, Inc dba Retina Associate or Southern California (01034) - Huntington Beach
  • Retina Consultants San Diego - Poway
  • Orange County Retina Medical Group - Santa Ana
  • Bay Area Retina Associates - Walnut Creek - Walnut Creek

Florida

  • Florida Retina Institute - Orlando (01053) - Orlando
  • Retina Specialty Institute - Pensacola - Pensacola
  • Retina Vitreous Associates of Florida (RVA) - Saint Petersburg - St. Petersburg

Arizona

  • Barnet Dulaney Perkins Eye Center (01018) - Mesa
  • Associated Retina Consultants - Phoenix - Phoenix

Colorado

  • Advanced Vision Research Institute - Longmont

Georgia

  • Southeast Retina Center - Augusta

Illinois

  • Illinois Retina Associates, S.C. - Oak Park (01061) - Oak Park

Indiana

  • Retina Consultants P.C. - Indianapolis

Louisiana

  • Retina Associates New Orleans - Jefferson Parish Location - Metairie

Trial Details

FieldValue
Enrollment Target 240 participants
Start Date 2025-06-23
Est. Completion 2027-11
Phase Phase 2
Apellis Pharmaceuticals

21 total trials

What NCT07215390 shows while recruiting

NCT07215390 is an interventional study that assigns participants to a tested intervention. The registered 240 participants enrollment target is mid-sized for trials with a published cap, above the 166-participant average among 4 other Geographic Atrophy Secondary to Age-related Macular Degeneration trials with a reported enrollment target (45% higher).

The record links to 1 condition, with Geographic Atrophy Secondary to Age-related Macular Degeneration appearing as the primary indexed condition, and to 2 interventions - of which APL-3007, pegcetacoplan (APL-2) is the first listed.

NCT07215390 names 20 study sites across 11 states, led by California, Florida, Arizona.

Frequently Asked Questions

What is clinical trial NCT07215390 about?

NCT07215390 is a clinical study titled "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". 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...

What is the current status of trial NCT07215390?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 240 participants. The study started on 2025-06-23. Estimated completion is 2027-11.

What conditions does trial NCT07215390 study?

This clinical trial studies the following conditions: Geographic Atrophy Secondary to Age-related Macular Degeneration.

What interventions are being tested in trial NCT07215390?

The interventions under investigation include: APL-3007, pegcetacoplan (APL-2) (DRUG), Placebo, Syfovre (OTHER).

Who is sponsoring clinical trial NCT07215390?

This trial is sponsored by Apellis Pharmaceuticals, which has 21 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07215390 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT07215390, the US trial registry maintained by the National Library of Medicine. NCT07215390 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.