Company intelligence / Profile preview
jCyte, Inc.
- 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 assets1 more asset in the full pipeline.
Partnerships
Beyond the preview
Go deeper on jCyte, Inc..
Explore clinical development, deal activity, and the competitive landscape with Gosset’s full data platform.
Clinical trials
Follow clinical development from trial design and recruitment through results.
- Trial phase
- Status
- Readouts
Licensing & deals
Explore licensing agreements, acquisitions, and the assets behind each deal.
- Partners
- Deal terms
- Milestones
Funding history
Trace financing activity and the investors behind a company’s development.
- Funding rounds
- Investors
- Capital raised
Competitive landscape
Compare peer pipelines by target, modality, and therapeutic area.
- Peer companies
- Targets
- Pipeline overlap
Technologies & patents
Explore technology platforms and the patent landscape around relevant assets.
- Platforms
- Patents
- Assignees
Research & analysis
Connect company news and source material to the questions you’re investigating.
- Company news
- Sources
- Analysis
Bring the full picture into focus.
See how Gosset can support your research on jCyte, Inc..