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jCyte, Inc.

Newport Beach, California, United Statesjcyte.com ↗

Ownership: Private
Development stage: Phase 3

Overview

jCyte’s lead program, jCell, has shown positive results in earlier clinical trials for retinitis pigmentosa. The company recently announced a positive pre–Phase 3 FDA Type B meeting and plans to advance to Phase 3 trials. There are currently no FDA-approved therapies for RP; the treatment uses minimally invasive intravitreal injection of allogeneic retinal progenitor cells to preserve or restore vision in patients with degenerative retinal diseases. In May 2020, a major licensing deal was signed with Santen Pharmaceutical for ex-US rights.

Therapeutic areas: Ophthalmology
Modalities: Allogeneic cell therapy (progenitor cell-based technology)
Industry: Biotech

Drug pipeline

2 assets

famzeretcel

1 more asset in the full pipeline.

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Partnerships

Santen Pharmaceutical Co., Ltd. – licensing/commercialization agreement for Europe and Asia worth up to $252 million plus royalties on net sales outside the US.

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