Nuvectis Pharma said it licensed exclusive rights outside China to two experimental drugs from Haisco, broadening its pipeline into complement-mediated diseases and cancer. The deal provides a strategic expansion for NVCT’s portfolio, with potential milestone and royalty opportunities if programs advance, though no terms were disclosed.
Nuvectis Pharma's NVCT stock fell 43.20% after Phase 1b study results. In interim data, efficacy was seen in 11 out of 12 patients. Thrombocytopenia issues were common but improved with a new dosing schedule. FDA granted Fast Track and Orphan Drug Designations for NXP800. Upcoming data expected in Q2 2025 from additional patient cohort.