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

Phase 2

Terminated

• Conditions: Geographic Atrophy; Macular Degeneration; Retinal Degeneration; Dry Age-related Macular Degeneration; Retinal Disease
• Interventions: Drug: GEM103

• Registration Number: NCT04643886
• Lead Sponsor: Gemini Therapeutics, Inc.

Brief Summary

This study is designed to investigate the safety, PK/PD, biomarker and early clinical effects of repeat GEM103 IVT injections.

Detailed Description

This is a Phase 2a, multi-center, open-label, multiple dose study in subjects with geographic atrophy (GA) secondary to dry Age-related Macular Degeneration (dry AMD) to investigate the safety, PK/PD, biomarker and early clinical effect of GEM103 repeat IVT injections.

Subjects will undergo clinical and ophthalmic assessments for determination of inclusion in the study. Subjects who participated in the Phase 1 Study (GEM-CL-10301) as well as treatment naïve subjects that did not participate in the GEM-CL-10301 Study and who meet all eligibility criteria will be enrolled.

Study Timeline

• Study Start: 2020-07-30
• Study First Submitted: 2020-11-16
• Study First Submitted QC: 2020-11-19
• Study First Posted: 2020-11-25
• Primary Completion: 2022-02-18
• Study Completion: 2022-03-21
• Status Verified: 2022-09
• Last Update Submitted: 2022-09-22
• Last Update Posted: 2022-09-23

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 62

Inclusion Criteria

1. At least 50 years old at the time of signed informed consent.

2. Must have one of the following genetic profiles:

   1. Genetic Profile A.
   2. Genetic Profile B.

3. BCVA in the study eye of 24 to 83 letters using ETDRS Chart Visual Acuity (VA) Scale (approximately equivalent to Snellen VA of 20/25 to 20/320).

4. Confirmed diagnosis of GA in the study eye where total size of all GA lesions in the study eye must be within 0.5 to 15.01- and 7- disc areas.

5. Sufficiently clear ocular media and able to cooperate with ophthalmic visual function testing and anatomic assessment in the study eye.

6. Understands the full nature and purpose of the study and provides informed consent prior to initiation of any study procedure; all subjects with a reproductive potential must agree to use effective contraceptive methods through the end of study (EOS) Visit.

Exclusion Criteria

1. Presence of the following ocular conditions - in the study eye:

   1. Any history of exudative Age-related Macular Degeneration or choroidal neovascularization.
   2. Any active ocular disease or condition that could confound the assessment of the macula or be a contraindication to IVT injection.
   3. Any intraocular surgery, with the exception of stable intraocular lens replacement surgery more than 3 months prior to consent.
   4. Aphakia or complete absence of the posterior capsule.
   5. History of laser therapy to the macula or fundus or extensive laser to the retina.
   6. Prior corneal transplant.

2. Presence of any of the following ocular conditions - in either eye:

   1. History of herpetic infection.
   2. Concurrent disease that could require medical or surgical intervention during the study period.
   3. Active uveitis and/or vitritis (grade: trace or above).
   4. History of idiopathic or autoimmune-associated uveitis.
   5. Active blepharitis, conjunctivitis, keratitis, episcleritis, scleritis, or endophthalmitis.
   6. Any ophthalmologic condition that reduces the clarity of the media and that, in the opinion of the Investigator, interferes with ophthalmologic examination.

3. In the opinion of the Investigator, the subject has any prior or ongoing medical condition (e.g., ocular other than dry AMD, systemic, psychiatric) or clinically significant screening laboratory value that may present a safety risk, interfere with study compliance or study follow-up, or confound data interpretation throughout the follow-up period.

4. Female subjects must not be pregnant or lactating, nor plan to become pregnant during the study.

5. Current use of medications known to be toxic to the lens, retina, or optic nerve.

6. Use of any investigational new drug or other experimental treatment in the last 6 months, and/or receipt of any prior gene therapy (e.g., AAV) or ocular device implantation (other than PCIOL placement following cataract surgery)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Cohort with Genetic Profile B	GEM103	Subjects will have Genetic Profile B. Intervention: Biological: GEM103
Cohort with Genetic Profile A	GEM103	Subjects will have Genetic Profile A. Intervention: Biological: GEM103.

Primary Outcome Measures

Name	Time	Method
Safety of intravitreal (IVT) injections of GEM103, as measured by number of subjects with ocular adverse events.	18 months

Secondary Outcome Measures

Name	Time	Method
To describe the clinical effect of GEM103 IVT injection, as the change from baseline in best corrected visual acuity (BCVA) scores as assessed by ETDRS scale.	6 months
To evaluate the total CFH levels in aqueous humor after GEM103 IVT injection, whenever possible.	6 months

Trial Locations

Locations (1)

Gemini Clinical Trial Site; 🇺🇸 Virginia Beach, Virginia, United States