Company intelligence / Profile preview
ReHeva Biosciences
- Ownership
- Private
- Development stage
- Phase 1
Overview
The company has successfully completed a Phase I safety and tolerability trial of its lead candidate RH324 in patients with advanced NSCLC who have failed prior treatments. The trial demonstrated safety at escalating doses and set the stage for upcoming efficacy studies. No major adverse events reported; further clinical data pending from planned Phase II studies.
- Therapeutic areas
- Oncology
- Modalities
- Botanical drugs (naturally occurring complex botanicals)
- Industry
- Biotech
Drug pipeline
1 assetPartnerships
Beyond the preview
Go deeper on ReHeva Biosciences.
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 ReHeva Biosciences.