drugset / Trial / NCT06804824

A First-in-Human (FIH) Study to Evaluate the Safety and Tolerability of VVD-159642 in Participants With Advanced Solid Tumors

NCT06804824

Phase 1 Recruiting 220 enrolled Vividion Therapeutics, Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

A FIH study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary anti-tumor activity of VVD-159642, a rat sarcoma viral oncogene-phosphatidylinositol 3-kinase alpha (RAS-PI3Kα) inhibitor, as a single agent and in combination with either sotorasib or trametinib in participants with advanced solid tumors.

Timeline

Start
2025-02-25
Primary completion
2027-08-01
Completion
2027-08-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Sotorasib Small molecule Oral
Subject Trametinib Small molecule Oral
Subject VVD-159642 Unknown Oral

Indications