Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07441642 · ClinicalTrials.gov registry record · Phase 2

A Study to Investigate Efficacy and Safety of FWY003 Compared With Placebo in Participants With Geographic Atrophy Secondary to Age-related Macular Degeneration

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

Recruiting
Registry status
Phase 2
Development phase
272
Enrollment target
4
Study locations

NCT07441642: Recruiting Phase 2 study of Geographic Atrophy Secondary to Age-related Macular Degeneration, sponsored by Novartis Pharmaceuticals.

NCT07441642 is a Phase 2 study of Geographic Atrophy Secondary to Age-related Macular Degeneration that is actively recruiting participants, run by Novartis Pharmaceuticals. The registered enrollment target is 272 participants, above the 158-participant average among 4 other Geographic Atrophy Secondary to Age-related Macular Degeneration trials with a reported enrollment target (72% higher). The trial reports 4 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07441642, a Phase 2 study of Geographic Atrophy Secondary to Age-related Macular Degeneration, is actively recruiting participants, sponsored by Novartis Pharmaceuticals.

RECRUITING
Registry status
Phase 2
Development phase
272 participants
Enrollment target
4
Study locations

Study Summary

To characterize the dose response relationship of FWY003 in participants with geographic atrophy (GA) secondary to age-related macular degeneration (AMD).

Primary Outcome

To evaluate the dose response relationship of FWY003 on GA lesion area in the study eye in participants with GA secondary to age-related macular degeneration (AMD).

Interventions

  • DRUG Placebo
  • DRUG FWY003

Study Locations (4)

Florida

  • Advanced Research LLC - Boynton Beach
  • Advanced Research LLC - Deerfield Beach

California

  • Salehi Retina Institute - Huntington Beach

Massachusetts

  • Opthamalic Consultants of Boston - Boston

Trial Details

FieldValue
Enrollment Target 272 participants
Start Date 2026-03-09
Est. Completion 2029-08-22
Phase Phase 2
Novartis Pharmaceuticals

1,375 total trials

What NCT07441642 shows while recruiting

NCT07441642 is an interventional study that assigns participants to a tested intervention. The registered 272 participants enrollment target is mid-sized for trials with a published cap, above the 158-participant average among 4 other Geographic Atrophy Secondary to Age-related Macular Degeneration trials with a reported enrollment target (72% 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 Placebo is the first listed.

NCT07441642 reports a single indexed study location in Florida, California, Massachusetts.

Frequently Asked Questions

What is clinical trial NCT07441642 about?

NCT07441642 is a clinical study titled "A Study to Investigate Efficacy and Safety of FWY003 Compared With Placebo in Participants With Geographic Atrophy Secondary to Age-related Macular Degeneration". To characterize the dose response relationship of FWY003 in participants with geographic atrophy (GA) secondary to age-related macular degeneration (AMD).

What is the current status of trial NCT07441642?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 272 participants. The study started on 2026-03-09. Estimated completion is 2029-08-22.

What conditions does trial NCT07441642 study?

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

What interventions are being tested in trial NCT07441642?

The interventions under investigation include: Placebo (DRUG), FWY003 (DRUG).

Who is sponsoring clinical trial NCT07441642?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07441642 being conducted?

This trial has 4 study locations across California, Florida, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Geographic Atrophy Secondary to Age-related Macular Degeneration

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02468024 · 272 participants · Phase 3

    JoLT-Ca Sublobar Resection (SR) Versus Stereotactic Ablative Radiotherapy (SAbR) for Lung Cancer

  • NCT05519449 · 272 participants · Phase 1

    Study of JANX007 in Subjects With Metastatic Castration-Resistant Prostate Cancer (ENGAGER-PSMA-01)

  • NCT06035939 · 272 participants · NA

    SMYLS Multi-site Trial

  • NCT06083051 · 272 participants · NA

    Differences in Postoperative Symptoms With Four Ureteral Stents

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT07441642, the US trial registry maintained by the National Library of Medicine. NCT07441642 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.