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NCT07441694

Study of INCA036978 in Participants With Myeloproliferative Neoplasms

Recruiting now Phase 1 Last updated 15 April 2026
What this trial tests

Phase 1 trial testing INCA036978 in Myeloproliferative Neoplasms in 218 participants. Currently enrolling.

Timeline
27 April 2026
Primary endpoint
24 May 2030
24 May 2030

Quick facts

Lead sponsorIncyte Corporation
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment218
Start date27 April 2026
Primary completion24 May 2030
Estimated completion24 May 2030
Sites47 locations across France, Italy, Belgium, United Kingdom, Germany, Canada, Australia, United States

Drugs / interventions tested

Conditions studied

Sponsor

Incyte Corporation — full company profile →

Who can join

18 and older, any sex, with Myeloproliferative Neoplasms. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will be conducted to determine the safety, tolerability, dose-limiting toxicity (DLT)s, and maximum tolerated dose (MTD) and/or recommended dose for expansion (RDE)s of INCA036978 administered as monotherapy and in combination with a standard disease-directed therapy.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Myeloproliferative Neoplasms

Currently open trials in the same condition.

Other Incyte Corporation trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07441694.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing