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Terminated Phase 2 Interventional Results available

A Multiple Dose Study of Repeat Intravitreal Injections of GEM103 in Neovascular Age-related Macular Degeneration

ClinicalTrials.gov ID: NCT04684394

Public ClinicalTrials.gov record NCT04684394. 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 24, 2026, 4:53 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 Multicenter, Multiple-Dose Study in Neovascular Age-related Macular Degeneration (nAMD) to Evaluate the Safety, Tolerability, Pharmacodynamics, Immunogenicity, and Clinical Effect of Repeat Intravitreal (IVT) Injections of GEM103 as an Adjunct to Standard of Care Aflibercept Therapy

Brief summary

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

This study is designed to investigate the safety and tolerability of GEM103 IVT injection + standard of care vs. sham + standard of care.

Study identification

NCT ID
NCT04684394
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gemini Therapeutics, Inc.
Industry
Enrollment
50 participants

Conditions and interventions

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
Dec 29, 2020 (Actual)
Primary completion
Jan 10, 2022 (Actual)
Completion
Feb 18, 2022 (Actual)
Last update posted
Oct 31, 2022

2020 – 2022

United States locations

U.S. sites
23
U.S. states
13
U.S. cities
22
Facility City State ZIP Site status
Gemini Clinical Trial Site 16 Phoenix Arizona 85021 —
Gemini Clinical Trial Site 11 Campbell California 95008 —
Gemini Clinical Trial Site 9 Encino California 91436 —
Gemini Clinical Trial Site 17 Huntington Beach California 92647 —
Gemini Clinical Trial Site 12 Pasadena California 91107 —
Gemini Clinical Trial Site 5 Miami Florida 33143 —
Gemini Clinical Trial Site 7 Pinellas Park Florida 33782 —
Gemini Clinical Trial Site 20 Sarasota Florida 34239 —
Gemini Clinical Trial Site 8 Stuart Florida 34994 —
Gemini Clinical Trial Site 18 Winter Haven Florida 33880 —
Gemini Clinical Trial Site 19 Indianapolis Indiana 46290 —
Gemini Clinical Trial Site 4 Hagerstown Maryland 21740 —
Gemini Clinical Trial Site 23 Worcester Massachusetts 01605 —
Gemini Clinical Trial Site 22 Royal Oak Michigan 48073 —
Gemini Clinical Trial Site 1 Reno Nevada 89502 —
Gemini Clinical Trial Site 2 Asheville North Carolina 28803 —
Gemini Clinical Trial Site 15 Charlotte North Carolina 28210 —
Gemini Clinical Trial Site 6 Cincinnati Ohio 45219 —
Gemini Clinical Trial Site 10 Eugene Oregon 97401 —
Gemini Clinical Trial Site 13 Beaufort South Carolina 29902 —
Gemini Clinical Trial Site 3 Dallas Texas 75231 —
Gemini Clinical Trial Site 21 San Antonio Texas 78240 —
Gemini Clinical Trial Site 14 San Antonio Texas 78247 —

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 NCT04684394, 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 Oct 31, 2022 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04684394 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →