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Active, not recruiting Phase 2 Interventional

Safety of a Single, Intravitreal Injection of 6.0M jCell (Famzeretcel) in Retinitis Pigmentosa (RP)

ClinicalTrials.gov ID: NCT06912633

Public ClinicalTrials.gov record NCT06912633. 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 20, 2026, 8:21 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 Randomized, Masked, Sham-Controlled Phase 2 Trial of the Safety of a Single Intravitreal Injection of jCell (Famzeretcel) for the Treatment of Retinitis Pigmentosa (RP)

Brief summary

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

This study evaluates the safety of a single injection of jCell (famzeretcel) comprising 6.0 million (6.0M) retinal progenitor cells over a six-month study period in a cohort of adult subjects with RP. Additionally, changes in visual function will be evaluated at six months between the active treatment group (6.0M jCell) compared to sham-treated controls.

Study identification

NCT ID
NCT06912633
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
jCyte, Inc
Industry
Enrollment
31 participants

Conditions and interventions

Interventions

Biological · Other

Eligibility (public fields only)

Age range
18 Years to 60 Years
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
Jun 20, 2025 (Actual)
Primary completion
Dec 2026 (Estimated)
Completion
Dec 2026 (Estimated)
Last update posted
Jul 30, 2026

2025 – 2026

United States locations

U.S. sites
12
U.S. states
8
U.S. cities
12
Facility City State ZIP Site status
Associated Retina Consultants Phoenix Arizona 85020 —
California Retina Consultants Bakersfield California 93309 —
Retina-Vitreous Associates Medical Group Beverly Hills California 90074 —
Gavin Herbert Eye Institute, UC Irvine Irvine California 92697 —
Retina Consultants Medical Group Sacramento California 95825 —
Vitreo Retinal Associates Gainesville Florida 32607 —
Illinois Retina Associates Oak Park Illinois 60304 —
NJRetina Teaneck New Jersey 07666 —
Long Island Vitreoretinal Consultants Westbury New York 11590 —
Retina Consultants of Texas: Bellaire Retina Center Bellaire Texas 77401 —
Retina Consultants of Texas: San Antonio San Antonio Texas 78240 —
The Retina Group of Washington Fairfax Virginia 22031 —

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 NCT06912633, 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 Jul 30, 2026 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06912633 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →