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Clinical Trials/EUCTR2014-005210-28-DE
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

Sponsor
niversity Medical Center Hamburg-Eppendorf

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