A Phase 1/2a Study of Subretinal Administration of OpCT-001 Photoreceptor Precursor Cells Derived From iPSCs in Patients With Primary Photoreceptor Disease

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

Study OpCT-001-101 is a Phase 1/2a first-in-human, multisite, 2-part interventional study to evaluate the safety, tolerability, and the effect on clinical outcomes of OpCT-001 in up to approximately 54 adults with primary photoreceptor (PR) disease. Phase 1 will focus on safety and features a dose-escalation design. Phase 2 is designed to gather additional safety data and assess the effect of OpCT-001 on measures of visual function, functional vision, and anatomic measures of engraftment in different clinical subgroups.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Confirmed genetic diagnosis of primary photoreceptor (PR) disease

• Best corrected visual acuity (BCVA) in the study eye at Screening for Phase 1: Logmarithm of the minimum angle of resolution (LogMAR) 3.9 to LogMAR 1.0. BCVA at Screening for Phase 2: ETDRS letter score 20 and 60.

• Retinal structure examination in the study eye demonstrating regions suitable for cell administration.

Locations
United States
Florida
University of Miami, Bascom Palmer Eye Institute
RECRUITING
Miami
Texas
Retina Foundation of the Southwest
RECRUITING
Dallas
Wisconsin
University of Wisconsin
RECRUITING
Madison
Contact Information
Primary
Patient Engagement
clinicaltrials@bluerocktx.com
1-857-299-7589
Time Frame
Start Date: 2025-03-10
Estimated Completion Date: 2030-10
Participants
Target number of participants: 54
Treatments
Experimental: Cohort 1
OpCT-001 dose level 1 will be administered via subretinal injection.
Experimental: Cohort 2
OpCT-001 dose level 2 will be administered via subretinal injection.
Experimental: Cohort 3
OpCT-001 dose level 3 will be administered via subretinal injection.
Experimental: Cohort 4
OpCT-001 dose level 4 will be administered via subretinal injection.
Sponsors
Leads: BlueRock Therapeutics

This content was sourced from clinicaltrials.gov

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