Ownership
Private
Therapeutic Areas
Stage
Phase 1
Preclinical
Phase 1
Phase 2
Phase 3
Approved
Modalities
Tavanta Therapeutics General Information
Tavanta has reported positive top-line results from its pivotal Phase III clinical trial for TAVT-45 (abiraterone acetate), which met its primary objective of establishing therapeutic equivalence to Zytiga® in patients with metastatic castrate-resistant prostate cancer and metastatic high-risk castrate-sensitive prostate cancer, with a comparable safety profile.
Contact Information
Website
Primary Industry
Biotech
Corporate Office
Media, Pennsylvania
United States
United States
Drug Pipeline
TAVT-135
Pre-clinicalKey Partnerships
Tavanta Therapeutics Funding
No funding data available
To view Tavanta Therapeutics's complete valuation and funding history, request access »
Gosset