Phase 1/2 Safety and Efficacy Study of AAV-RPE65 Vector to Treat Leber Congenital Amaurosis

Phase 1

Completed

Brief Summary: The purpose of the study is to evaluate the safety and efficacy of an adeno-associated virus vector expressing RPE65 in patients with Leber congenital amaurosis caused by mutations in the RPE65 gene.

Funding Source - FDA OOPD

Detailed Description: This will be a non-randomized, open label study. A total of 12 participants will be enrolled into two groups of 6 each. Each participant will receive rAAV2 CB hRPE65 by subretinal injection in one eye on a single occasion. Participants in Group 1 will receive 450 µL at a dosage level of 4 x 10\^11 vg/mL containing a total of 1.8 x 10\^11 vg of rAAV2-CB-hRPE65. Participants in Group 2 will receive 450 µL at a dosage level of 1.33 x 10\^12 vg/mL containing a total of 6 x 10\^11 vg of rAAV2-CB-hRPE65. A retinal surgeon will administer the vector by subretinal injection.

Enrollment will begin with Group 1 and will proceed to Group 2 after review of safety data by a Data and Safety Monitoring Committee.

Safety will be monitored by evaluation of ocular and non ocular adverse events and hematology and clinical chemistry parameters. Efficacy will be measured by evaluation of visual fields, visual acuity and electroretinography.

Recruitment & Eligibility

Inclusion Criteria

Retinal disease consistent with a diagnosis of Leber congenital amaurosis and documented mutations in the RPE65 gene (including null mutations and mutations that code for abnormal RPE65 protein);
At least 6 years of age;
Good general health without significant physical examination findings or clinically significant abnormal laboratory results;
Able to perform tests of visual and retinal function;
Visual acuity not better than 20/60 and not worse than hand motion in both the treated eye and the fellow eye;
Visible photoreceptor (outer nuclear) layer on a standard optical coherence tomography (OCT) scan;
Acceptable hematology, clinical chemistry and urine laboratory parameters;
For females of childbearing potential, a negative pregnancy test at screening and at baseline, and agreement to use effective contraception for 12 months after administration of rAAV2-CB-hRPE65, for sexual activity that could lead to pregnancy;
For males of reproductive potential, agreement to use effective contraception for 12 months after administration of rAAV2-CB-hRPE65, for sexual activity that could lead to pregnancy

Exclusion Criteria

Pre-existing eye conditions that would preclude the planned surgery or interfere with interpretation of study endpoints or complications of surgery (e.g. glaucoma, corneal or lenticular opacities, or history or retinal detachment);
Presence of epiretinal membrane on OCT;
History of immunodeficiency or other medical conditions that might increase the risk of rAAV2-CB-hRPE65 administration;
Use of anticoagulants or anti-platelet agents within 7 days prior to study agent administration;
History of allergy or sensitivity to medications planned for use in the peri-operative period;
For females of childbearing potential, a positive pregnancy test at screening or baseline (within 2 days before rAAV2-CB-hRPE65 administration);
Females who are breast feeding;
Use of any investigational agent, or systemic corticosteroids or other immunosuppressive drug(s), within 3 months prior to enrollment;
Prior receipt of any AAV gene therapy product;
Any condition which leads the investigator to believe that the participant cannot comply with the protocol requirements or that may place the participant at an unacceptable risk for participation.

Arm && Interventions

Group	Intervention	Description
1	rAAV2-CB-hRPE65	Subjects at least 6 y/o treated with a lower dose of the vector by subretinal injection
2	rAAV2-CB-hRPE65	Subjects at least 6 y/o treated with a higher dose of the vector by subretinal injection

Primary Outcome Measures

Name	Time	Method
Number of Participants Experiencing Ocular or Non-ocular Adverse Events	2 years

Secondary Outcome Measures

Name	Time	Method
Participants With Changes in Best Corrected Visual Acuity	2 years	Increase in BCVA of 7 or more letters at Year 2 visit compared to average baseline value
Participants With Changes in Visual Fields	2 years	Improvement in the central 30 degree visual field, measured by static perimetry, at one or more time points after treatment, that was greater than the limit of agreement for baseline values .

Locations (2): Casey Eye Institue, Oregon Health & Science University
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Portland, Oregon, United States
University of Massachusetts Medical School
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Worcester, Massachusetts, United States