NCT06804824 2026-03-18
A First-in-Human (FIH) Study to Evaluate the Safety and Tolerability of VVD-159642 in Participants With Advanced Solid Tumors
Vividion Therapeutics, Inc.
Phase 1 Recruiting
Vividion Therapeutics, Inc.
Boehringer Ingelheim
Amgen
China Medical University Hospital
Tianjin Medical University Second Hospital
National Cancer Institute (NCI)
Shanghai Henlius Biotech
Novartis
GlaxoSmithKline