EUCTR2014-005210-28-DEActive, not recruitingPhase 1
Ruxolitinib versus allogeneic stem cell transplantation for patients with myelofibrosis according to donor availability: A prospective phase II trial (MMM 02 study) - Ruxolitinib versus allogeneic stem cell transplantation
niversity Medical Center Hamburg-Eppendorf0 sites155 target enrollmentStarted: December 23, 2015Last updated:
Conditions
Drugs
Trial Snapshot
- Phase
- Phase 1
- Status
- Active, not recruiting
- Sponsor
- Enrollment
- 155
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •1.Symptomatic primary myelofibrosis or myelofibrosis post polycythaemia vera or essential thrombocythemia stage intermediate 2- or high-risk according to IPSS or DIPSS [46] or inter-mediate 1-risk with high risk cytogenetics, other than normal karyotype, sole del 20q, del 13q, or sole +9, or transfusion-dependency
- •2.Patients age: 18 - 70 years at time of inclusion (female and male)
- •3.Patients understand and voluntarily sign an informed consent form
- •4.Platelet count = 50 x 109/L
- •5.No prior Ruxolitinib treatment
- •6.ECOG = 2
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 100
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 55
Exclusion Criteria
- •1.Severe renal, hepatic, pulmonary or cardiac disease, such as:
- •Total bilirubin, SGPT or SGOT > 3 times upper the normal level
- •Left ventricular ejection fraction < 30 %
- •Creatinine clearance < 30 ml/min
- •DLCO < 35 % and/or receiving supplementary continuous oxygen
- •2.Positive serology for HIV
- •3.Pregnant or lactating women (positive serum pregnancy test)
- •4.Age < 18 and = 71 years.
- •5.Uncontrolled invasive fungal infection at time of screening (baseline)
- •6.Serious psychiatric or psychological disorders
- •7.Participation in another study with ongoing use of unlicensed investigational product from 28 days before study enrollment
- •8.Transformation to AML
Investigators
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