clinical trial · NCT06034002
A Study to Evaluate INCA033989 Administered as a Monotherapy or in Combination With Ruxolitinib in Participants With Myeloproliferative Neoplasms
Myeloproliferative NeoplasmsINCA033989Ruxolitinib
brief 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.
started
Dec 4, 2023
primary completion
Oct 29, 2028
completion
Oct 29, 2028
last updated
Apr 17, 2026
official title
A Phase 1, Open-Label, Multicenter Study of INCA033989 Administered as a Monotherapy or in Combination With Ruxolitinib in Participants With Myeloproliferative Neoplasms
sourced from ClinicalTrials.gov · pharmadog mirrors structured fields, not the full protocol