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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT03295877
Recruitment Status : Completed
First Posted : September 28, 2017
Last Update Posted : February 12, 2020
Information provided by (Responsible Party):
Genentech, Inc.

Brief Summary:
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.

Condition or disease Intervention/treatment Phase
Geographic Atrophy Drug: RO7171009 Phase 1

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 28 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
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
Actual Study Start Date : September 21, 2017
Actual Primary Completion Date : November 20, 2018
Actual Study Completion Date : November 20, 2018

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Experimental: RO7171009: SAD
Patients will receive a single dose of RO7171009, in multiple escalating cohorts.
Drug: RO7171009
Patients will receive RO7171009 via ITV injection.

Experimental: RO7171009: MD
Patients will receive RO7171009 at maximum tolerated dose (MTD), identified during the SAD stage for three doses.
Drug: RO7171009
Patients will receive RO7171009 via ITV injection.

Primary Outcome Measures :
  1. Safety and Tolerability of the Study Drug: Rate of Adverse Events [ Time Frame: Through study completion or early study discontinuation (overall 12-20 weeks) ]

Secondary Outcome Measures :
  1. Serum Concentration of RO7171009 [ Time Frame: Through study completion or early study discontinuation (overall 12-20 weeks) ]

Information from the National Library of Medicine

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Ages Eligible for Study:   50 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Participants aged greater than or equal to (>/=) 50 years
  • Well demarcated area(s) of GA secondary to AMD with no evidence of prior or active choroidal neovascularization (CNV) in study eye

Exclusion Criteria:

Ocular Exclusion Criteria, Study Eye:

  • History of vitrectomy surgery, submacular surgery, or other surgical intervention for AMD
  • Previous laser photocoagulation for CNV, diabetic macular edema, retinal vein occlusion, or proliferative diabetic retinopathy
  • Prior treatment with Visudyne®, external beam radiation therapy (for intraocular conditions), or transpupillary thermotherapy

Ocular Exclusion Criteria (Both Eyes):

  • GA in either eye due to causes other than AMD
  • Evidence of prior or active CNV
  • Previous participation in interventional clinical trials for GA or dry AMD, except for vitamins and minerals, irrespective of the route of administration (i.e., ocular or systemic) within the last 6 months

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03295877

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United States, California
California Retina Consultants
Bakersfield, California, United States, 93309
Northern California Retina Vitreous Associates
Mountain View, California, United States, 94040
Retinal Consultants Med Group
Sacramento, California, United States, 95825
California Retina Consultants
Santa Barbara, California, United States, 93103
California Retina Consultants - Santa Maria
Santa Maria, California, United States, 93454
United States, Colorado
Retina Consultants of Southern Colorado PC; Clinical Research Department
Colorado Springs, Colorado, United States, 80909-1183
United States, Florida
Florida Eye Associates
Melbourne, Florida, United States, 32901
Retina Specialty Institute
Pensacola, Florida, United States, 32503
United States, Georgia
Georgia Retina PC
Marietta, Georgia, United States, 30060
United States, Missouri
The Retina Institute
Saint Louis, Missouri, United States, 63128
United States, Nevada
Sierra Eye Associates
Reno, Nevada, United States, 89502
United States, North Carolina
Western Carolina Retinal Associate PA
Asheville, North Carolina, United States, 28803
United States, Tennessee
Tennessee Retina PC.
Nashville, Tennessee, United States, 37203
Sponsors and Collaborators
Genentech, Inc.
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Study Director: Clinical Trials Hoffmann-La Roche
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Responsible Party: Genentech, Inc.
ClinicalTrials.gov Identifier: NCT03295877    
Other Study ID Numbers: GR39821
First Posted: September 28, 2017    Key Record Dates
Last Update Posted: February 12, 2020
Last Verified: February 2020

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Macular Degeneration
Geographic Atrophy
Retinal Degeneration
Retinal Diseases
Eye Diseases
Pathological Conditions, Anatomical