ClinicalTrials.gov record
Active, not recruiting Phase 1 Interventional

A Study to Investigate Safety, Tolerability, Pharmacokinetics (PK), Pharmacodynamics (PD), and Immunogenicity of RO7669330 in Participants With Geographic Atrophy (GA) Secondary to Age-related Macular Degeneration (AMD)

ClinicalTrials.gov ID: NCT06961370

Public ClinicalTrials.gov record NCT06961370. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 8, 2026, 8:08 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase I, Multi-center, Multi-part Study to Investigate Safety, Tolerability, PK, PD, and Immunogenicity of RO7669330 Intravitreal Injections in Participants With GA Secondary to AMD: Part 1A: Open-label, MAD; Part 1B: Randomized PD Pilot; Part 2: Masked, Randomized, Active-comparator-controlled

Study identification

NCT ID
NCT06961370
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
27 participants

Conditions and interventions

Interventions

  • Izervay™ Drug
  • RO7669330 Drug
  • Syfovre™ Drug

Drug

Eligibility (public fields only)

Age range
55 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 15, 2025
Primary completion
Jan 2, 2027
Completion
Jan 2, 2027
Last update posted
May 6, 2026

2025 – 2027

United States locations

U.S. sites
16
U.S. states
9
U.S. cities
16
Facility City State ZIP Site status
Associated Retina Consultants - Phoenix - DocTrials - PPDS Phoenix Arizona 85020-5505
Barnet Dulaney Perkins Eye Center Sun City Arizona 85351
Retina-Vitreous Associates Medical Group Beverly Hills California 90211
Global Research Management Glendale California 91204
Retinal Consultants Medical Group Inc - Parkcenter Drive Sacramento California 95825
Southeast Retina Center Augusta Georgia 30909
Cumberland Valley Retina Consultants PC Hagerstown Maryland 21740
The Retina Institute St Louis Missouri 63128
Retina Northwest Portland Oregon 97221
Erie Retina Research Erie Pennsylvania 16505
Charles Retina Institute Germantown Tennessee 38138
Tennessee Retina PC Nashville Tennessee 37203
Austin Clinical Research, LLC Austin Texas 78750
Texas Retina Associates Dallas Texas 75231
Retina Consultants of Texas Westover Hills Retina Center San Antonio Texas 78251
Retina Consultants of Texas - (The Woodlands) The Woodlands Texas 77384

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06961370, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 6, 2026 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06961370 live on ClinicalTrials.gov.

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