drugset / Trial / NCT05954312

A First-in-Human (FIH) Study to Evaluate the Safety and Tolerability of VVD-130037 in Participants With Advanced Solid Tumors

NCT05954312 ↗

Phase 1 Recruiting 290 enrolled Vividion Therapeutics, Inc.
RandomizedSequentialOpen-labelTreatment

Summary

A FIH dose escalation and dose expansion study to evaluate VVD-130037 in participants with advanced solid tumors as a single agent, and in combination with docetaxel, paclitaxel, or pembrolizumab.

Timeline

Start
2023-07-28
Primary completion
2030-08-31
Completion
2031-02-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel Small molecule — Intravenous
Subject Paclitaxel Small molecule — Intravenous
Subject Pembrolizumab Monoclonal antibody — Intravenous
Subject VVD-130037 Unknown — Oral

Indications