Active, not recruitingPhase 3NCT04027309

A Study of Gilteritinib Versus Midostaurin in Combination With Induction and Consolidation Therapy Followed by One-year Maintenance in Patients With Newly Diagnosed Acute Myeloid Leukemia or Myelodysplastic Syndromes With Excess Blasts-2 With FLT3 Mutations Eligible for Intensive Chemotherapy

Studying Acute promyelocytic leukemia

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Key facts

Sponsor
Stichting Hemato-Oncologie voor Volwassenen Nederland
Principal Investigator
M. Raaijmakers, Prof. Dr.
Erasmus MC / HOVON
Intervention
Gilteritinib(drug)
Enrollment
777 enrolled
Eligibility
18 years · All sexes
Timeline
20192033

Study locations (30)

Collaborators

Deutsch-Österreichische Studiengruppe Akute Myeloische Leukämie (AMLSG) · Astellas Pharma Global Development, Inc.

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT04027309 on ClinicalTrials.gov

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