Blood

Chronic mast cell leukemia

ORPHA:566396 ↗Gene KITClinical subtype

6

studies recruiting now

as of 7 Sept 2026

54

studies registered in total

as of 7 Sept 2026

14

countries with a recruiting site

as of 7 Sept 2026

27 Aug 2025

most recent study posted

among recruiting studies

Recruiting trials

Showing the 5 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.

See all 6 recruiting studies

Where recruiting studies are running

Countries with at least one recruiting site among the studies above, 7 Sept 2026. Tap a country to search trials there.

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Patient organisations

We do not yet list a dedicated organisation for this condition. The directories below are the best route.

About Chronic mast cell leukemia

RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the gene involved (KIT).

Treatments being studied

14 approved treatments and 51 in clinical development, from Open Targets (CC BY 4.0). Not medical advice.

Approved: Imatinib Mesylate (Gleevec)Approved: Omacetaxine Mepesuccinate (Synribo)Approved: Bosutinib Monohydrate (Bosulif)Approved: Hydroxyurea (Droxia)Approved: Interferon Alfa-N1 (Well-feron)Approved: Dasatinib (Dasatinib accord healthcare)Approved: NilotinibApproved: Nilotinib Hydrochloride Monohydrate (Tasigna)Approved: Busulfan (Busilvex)Approved: Asciminib Hydrochloride (Scemblix)Approved: Ponatinib Hydrochloride (Iclusig)Approved: AsciminibApproved: Dasatinib Anhydrous (Dasatinib accord)Approved: Imatinib
Phase 3Olverembatinib
Phase 3Cytarabine (Alexan)
Phase 3Cyclophosphamide (Cyclophosphamide)
Phase 3Sargramostim (Leukine)
Phase 3Interferon Alfa
Phase 3Bosutinib
Phase 3Peginterferon Alfa-2a (Pegasys)
Phase 3Ponatinib (Iclusig)

+ 43 more in development

Related conditions

Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).