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Clinical Trials/NCT02145026
NCT02145026
Completed
Phase 4

A Prospective Open-Label Study of the Effectiveness of Epoetin Beta for Treating Anemic Patients With Low/Intermediate-1-Risk Myelodysplastic Syndrome (MDS)

Hoffmann-La Roche10 sites in 1 country100 target enrollmentAugust 6, 2014

Overview

Phase
Phase 4
Intervention
Epoetin beta
Conditions
Myelodysplastic Syndromes
Sponsor
Hoffmann-La Roche
Enrollment
100
Locations
10
Primary Endpoint
Proportion of Participants Achieving Erythroid Response at Week 12 as Assessed by International Working Group (IWG) 2006 Response Criteria
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This is a Phase IV, prospective, multi-center, open-label study to assess the effectiveness and safety profile of epoetin beta (Recormon®) for treatment of symptomatic anemia in adult participants associated with low/intermediate-1-risk MDS. After screening, eligible participants will be treated with epoetin beta as recommended in the approved label and international guidelines for the use of epoetin in MDS participants and the dosage will be adjusted on the basis of erythroid response.

Registry
clinicaltrials.gov
Start Date
August 6, 2014
End Date
April 9, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult participants with low or intermediate-1 risk MDS
  • No previous treatment with hematopoietic growth factors within 3 months prior to screening
  • Symptomatic anemia (hemoglobin \<10 g/dL) as determined by investigator
  • Serum erythropoietin \<500 milliunits/milliliter (mU/mL) within 14 days prior to the first dose of study treatment
  • Require no red blood cell transfusion or dependent on \<4 units within 8 weeks prior to screening
  • Clinically stable for at least 1 month prior to entry into the study
  • For female participants of childbearing potential and male participants with partners of childbearing potential, agreement (by participants and/or partner) to use highly effective form(s) of contraception

Exclusion Criteria

  • Contraindications and/or known hypersensitivity to the active substance and/or any of the excipients of epoetin beta treatment
  • Poorly controlled hypertension as assessed by the investigator
  • History of Acute Myeloid Leukemia (AML) or high risk for AML
  • Administration of another investigational drug within 1 month before screening or planned during the study period
  • Previously documented evidence of Pure Red Cell Aplasia (PRCA)

Arms & Interventions

Epoetin Beta

Participants will receive epoetin beta at an initial dose of 30,000 International Units (IU) per week administered subcutaneously (SC). Response will be firstly evaluated at Week 4 and the subsequent dose will be based on the response: if hemoglobin level reaches greater than or equal to (\>/=)12 grams per deciliter (g/dL) at any time, epoetin beta will be discontinued until hemoglobin levels are less than or equal to (\</=) 10 g/dL; if the hemoglobin level increases less than (\<) 1 g/dL from screening level and hemoglobin level ˂12 g/dL, a 60,000 IU per week epoetin beta will be administered SC until Week 12; if the hemoglobin level increases \>/=1 g/dL from screening level and hemoglobin level ˂12 g/dL, a 30,000 IU per week epoetin beta will be continued until Week 12.

Intervention: Epoetin beta

Outcomes

Primary Outcomes

Proportion of Participants Achieving Erythroid Response at Week 12 as Assessed by International Working Group (IWG) 2006 Response Criteria

Time Frame: Week 12

Erythroid response at Week 12 according to IWG 2006 criteria was defined as a hemoglobin (Hb) increase of \>/= 1.5 grams/deciliter (g/dL), and a reduction of units of red blood cell (RBC) transfusions by at least 4 transfusions/8 weeks compared with the pre-treatment transfusion number in the previous 8 weeks. Only RBC transfusions given for an Hb of \</= 9.0 g/dL pre-treatment were counted in the RBC transfusion response evaluation.

Secondary Outcomes

  • Percentage of Participants With Neutrophil Response (in Participants With Pre-Treatment Neutrophil <1.0*10^9 Per Liter) at Week 12 as Assessed by IWG 2006 Response Criteria(Week 12)
  • Percentage of Participants With Adverse Events(From signing of informed consent up to 4 weeks after last dose (up to 18 weeks))
  • Percentage of Participants With Platelet Response (in Participants With Pre-Treatment Platelets <100*10^9 Per Liter) at Week 12 as Assessed by IWG 2006 Response Criteria(Week 12)

Study Sites (10)

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