Usher Syndrome Clinical Trials

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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 (4) 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 approximately 54 adults with primary photoreceptor (PR) disease. Phase 1 focuses 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 1.3. BCVA at Screening for Phase 2: ETDRS letter score between 20 to 60, inclusive.

• 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
Pennsylvania
Mid Atlantic Retina/ Wills Eye
RECRUITING
Philadelphia
Texas
Retina Foundation of the Southwest
RECRUITING
Dallas
Wisconsin
University of Wisconsin
RECRUITING
Madison
Contact Information
Primary
Patient Engagement
clinicaltrials@bluerocktx.com
1-877-380-3931
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 (optional)
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