drugset / Trial / NCT06034002

A Study to Evaluate INCA033989 Administered as a Monotherapy or in Combination With Ruxolitinib in Participants With Myeloproliferative Neoplasms

NCT06034002

Phase 1 Recruiting 290 enrolled Incyte Corporation
Non-randomizedSequentialOpen-labelTreatment

Summary

This study is being conducted to evaluate the safety, tolerability, dose-limiting toxicity (DLT) and determine the maximum tolerated dose (MTD) and/or recommended dose(s) for expansion (RDE) of INCA033989 administered as a Monotherapy or in Combination With Ruxolitinib in participants with myeloproliferative neoplasms.

Timeline

Start
2023-12-04
Primary completion
2028-10-29
Completion
2028-10-29

Drugs

EvaluationDrugModalityDoseRoute
Subject INCA033989 Unknown
Subject Ruxolitinib Small molecule