drugset / Trial / NCT05665530

A Study of PRT2527 as Monotherapy and in Combination With Zanubrutinib or Venetoclax in Participants With R/R Hematologic Malignancies

NCT05665530

Phase 1 Completed 86 enrolled Prelude Therapeutics BeiGene · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a Phase 1 dose-escalation study of PRT2527, a potent and highly selective cyclin-dependent kinase (CDK) 9 inhibitor, in participants with select relapsed or refractory (R/R) hematologic malignancies. The purpose of this study is to evaluate the safety, tolerability, recommended phase 2 dose (PR2D), and preliminary efficacy of PRT2527 as a monotherapy and in combination with zanubrutinib or venetoclax.

Timeline

Start
2023-09-12
Primary completion
2025-06-12
Completion
2026-01-21

Drugs

EvaluationDrugModalityDoseRoute
Subject PRT2527 Unknown Intravenous
Subject Venetoclax Small molecule Oral
Subject Zanubrutinib Small molecule Oral