drugset / Trial / NCT05252416

(VELA) Study of BLU-222 in Advanced Solid Tumors

NCT05252416

Phase 1 Terminated 50 enrolled Blueprint Medicines Corporation
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a Phase 1/2, open-label, first-in-human (FIH) study designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and anticancer activity of BLU-222, a selective inhibitor of CDK2.

Timeline

Start
2022-04-07
Primary completion
2025-07-04
Completion
2025-07-04

Drugs

EvaluationDrugModalityDoseRoute
Subject CERTOCICLIB Small molecule Oral
Subject Carboplatin Small molecule Intravenous
Subject Fulvestrant Small molecule Intramuscular
Subject Ribociclib Small molecule Oral