Company intelligence / Profile preview
MyoPax
- Ownership
- Private
- Development stage
- Preclinical
Overview
MyoPax has received FDA Orphan Drug Designation and Rare Pediatric Disease Designation for its lead regenerative cell therapy targeting Exstrophy-Epispadias Complex. The company’s proprietary approach uses patient-specific, highly regenerative muscle stem cells. The first-in-human MuST clinical trial for EEC repair began in Germany with academic sponsorship. Other pipeline assets remain preclinical.
- Therapeutic areas
- OtherRare DiseasesNeurology
- Modalities
- Stem cell therapyCRISPR/Cas9
- Industry
- Biotech
Drug pipeline
2 assets1 more asset in the full pipeline.
Request access →Partnerships
Beyond the preview
Go deeper on MyoPax.
Explore clinical development, deal activity, and the competitive landscape with Gosset’s full data platform.
Clinical trials
Full profile accessFollow clinical development from trial design and recruitment through results.
- Trial phase
- Status
- Readouts
Licensing & deals
Full profile accessExplore licensing agreements, acquisitions, and the assets behind each deal.
- Partners
- Deal terms
- Milestones
Funding history
Full profile accessTrace financing activity and the investors behind a company’s development.
- Funding rounds
- Investors
- Capital raised
Competitive landscape
Full profile accessCompare peer pipelines by target, modality, and therapeutic area.
- Peer companies
- Targets
- Pipeline overlap
Technologies & patents
Full profile accessExplore technology platforms and the patent landscape around relevant assets.
- Platforms
- Patents
- Assignees
Research & analysis
Full profile accessConnect 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 MyoPax.