drugset / Trial / NCT06188208

A First-in-Human (FIH) Study to Evaluate the Safety and Tolerability of VVD-130850 in Participants With Advanced Solid and Hematologic Tumors

NCT06188208 ↗

Phase 1 Terminated 132 enrolled Vividion Therapeutics, Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

A FIH study to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of VVD-130850, as single agent and in combination with checkpoint inhibition, in participants with advanced solid and hematologic tumors.

Timeline

Start
2024-01-05
Primary completion
2026-02-20
Completion
2026-02-20

Outcome

Outcome not reported

Stopped: “The study has ended”

Drugs

EvaluationDrugModalityDoseRoute
Subject Pembrolizumab Monoclonal antibody — Intravenous
Subject VVD-130850 Unknown — Oral