Study of INCA036978 in Participants With Myeloproliferative Neoplasms

Recruiting Phase 1 Interventional Study
Myeloproliferative Neoplasms
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
218 (estimated)
Sponsor
Incyte Corporation · Industry
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About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Life expectancy \> 6 months. * Willingness to undergo a pretreatment and limited on-study BM biopsies and aspirates (as appropriate to disease). * Participants with MF, PV and ET as defined in the protocol. Exclusion Criteria: * Presence of any hematological malignancy other…
Contacts

Incyte Corporation Call Center (US)

1.855.463.3463

medinfo@incyte.com

CONTACT

Incyte Corporation Call Center (ex-US)

+800 00027423

eumedinfo@incyte.com

CONTACT