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Completed Phase 1 Interventional

Safety and Tolerability Study of RO7171009 in Participants With Geographic Atrophy (GA) Secondary to Age-Related Macular Degeneration (AMD)

ClinicalTrials.gov ID: NCT03295877

Public ClinicalTrials.gov record NCT03295877. 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 Oct 25, 2026, 4:45 PM 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, Multicenter, Open-Label, Single-Dose, Dose-Escalation, and Multiple-Dose Study of the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of Intravitreal Injections of RO7171009 in Patients With Geographic Atrophy Secondary to Age-Related Macular Degeneration

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This Phase 1, open-label, multicenter study will investigate the safety and tolerability of RO7171009 following single and multiple intravitreal (ITV) administrations in patients with GA secondary to AMD. The study consists of two stages: Single Dose-Escalation (SAD) and Multiple-Dose (MD) stages.

Study identification

NCT ID
NCT03295877
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Genentech, Inc.
Industry
Enrollment
28 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
50 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
Sep 21, 2017 (Actual)
Primary completion
Nov 20, 2018 (Actual)
Completion
Nov 20, 2018 (Actual)
Last update posted
Feb 12, 2020

2017 – 2018

United States locations

U.S. sites
13
U.S. states
8
U.S. cities
13
Facility City State ZIP Site status
California Retina Consultants Bakersfield California 93309 —
Northern California Retina Vitreous Associates Mountain View California 94040 —
Retinal Consultants Med Group Sacramento California 95825 —
California Retina Consultants Santa Barbara California 93103 —
California Retina Consultants - Santa Maria Santa Maria California 93454 —
Retina Consultants of Southern Colorado PC; Clinical Research Department Colorado Springs Colorado 80909-1183 —
Florida Eye Associates Melbourne Florida 32901 —
Retina Specialty Institute Pensacola Florida 32503 —
Georgia Retina PC Marietta Georgia 30060 —
The Retina Institute St Louis Missouri 63128 —
Sierra Eye Associates Reno Nevada 89502 —
Western Carolina Retinal Associate PA Asheville North Carolina 28803 —
Tennessee Retina PC. Nashville Tennessee 37203 —

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 NCT03295877, 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 Feb 12, 2020 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03295877 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →