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RECRUITINGPhase 1/2

Clinical Trial of VBC103 in Patients With Advanced Malignant Solid Tumors

NCT07299747

This study is a multicenter, open-label, multi-dose, first-in-human (FIH) Phase I/IIa study to determine the safety and tolerability of VBC103, as well as the maximum tolerated dose (MTD) and/or recommended Phase II dose (RP2D), PK and further evaluate its efficacy.

Participants With Advanced Solid Tumor Malignancies

VelaVigo Bio Inc255 participantsStarted Dec 2025

Shanghai, Shanghai Municipality, China

Data from ClinicalTrials.govTerms