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Clinical Trial Summary

This study evaluates the safety and potential activity of a single dose of live human retinal progenitor cells (jCell) administered to adults with retinitis pigmentosa. Four different dose levels of cells will be assessed in each of two groups of patients.


Clinical Trial Description

The primary purpose of this study is to test the safety and tolerability of the administration of a single dose of jCell to adults with retinitis pigmentosa.

The goal of jCell therapy is to preserve vision by intervening in the disease at a time when host photoreceptors can be protected and potentially reactivated.

Human allogeneic retinal progenitor cells will be injected into adults with advanced RP to see if the procedure is safe, if the cells survive, and whether they have any impact on the visual status of the patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02320812
Study type Interventional
Source jCyte, Inc
Contact
Status Completed
Phase Phase 1/Phase 2
Start date June 2015
Completion date July 19, 2017

See also
  Status Clinical Trial Phase
Active, not recruiting NCT03975543 - Retrospective Natural History Study of Retinitis Pigmentosa
Recruiting NCT04763369 - Investigation of Therapeutic Efficacy and Safety of UMSCs for the Management of Retinitis Pigmentosa (RP) Phase 2
Completed NCT01543906 - Oral QLT091001 in Retinitis Pigmentosa (RP) Subjects With an Autosomal Dominant Mutation in Retinal Pigment Epithelial 65 Protein (RPE65) Phase 1
Completed NCT02575430 - Natural History Study in Inherited Retinal Disease Subjects Caused by Mutations in RPE65 or LRAT N/A