Company intelligence / Profile preview
Claruvis Pharmaceutical
Chongqing, Chongqing Shi, China
- Ownership
- Private
- Development stage
- Other
01
Overview
Claruvis Pharmaceutical has completed Phase III studies for its lead recombinant botulinum toxin type A product (YY001/YY003) for glabellar lines, meeting all primary endpoints in China; it also gained U.S. FDA IND approval and is pursuing a BLA supported by successful Phase I/II/III studies. Phase II trials for upper limb spasticity are ongoing.
- Therapeutic areas
- NeurologyDermatology
- Modalities
- Recombinant proteinToxinBiologic
- Industry
- Biotech
02
Drug pipeline
2 assets1 more asset in the full pipeline.
Request access →Beyond the preview
Go deeper on Claruvis Pharmaceutical.
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 Claruvis Pharmaceutical.