Efficacy and Safety of Activated Recombinant Human Factor VII in Treatment of Bleeding in Patients Following Allogeneic Stem Cell Transplantation
Phase 2
Completed
- Conditions
- Acquired Bleeding DisorderBleeding During/Following Surgery
- Interventions
- Procedure: standard therapyDrug: activated recombinant human factor VIIDrug: placebo
- Registration Number
- NCT01562158
- Lead Sponsor
- Novo Nordisk A/S
- Brief Summary
This trial is conducted in Asia, Europe and Oceania. The aim of this trial is to evaluate the efficacy of placebo and activated recombinant human factor VII in patients having undergone allogeneic or autologous stem cell transplantation.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
- Patients who have undergone allogeneic or autologous stem cell transplantation
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Exclusion Criteria
- Known or suspected allergy to trial product
- Participation in other trials with unapproved drugs or trials with equal or similar objective
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo standard therapy - Low dose standard therapy - Low dose activated recombinant human factor VII - High dose activated recombinant human factor VII - Medium dose activated recombinant human factor VII - High dose standard therapy - Placebo placebo - Medium dose standard therapy -
- Primary Outcome Measures
Name Time Method Effect on bleeding, defined as change in bleeding score
- Secondary Outcome Measures
Name Time Method Bleeding evaluation Transfusion requirements Adverse events
Trial Locations
- Locations (1)
Novo Nordisk Investigational Site
🇬🇧Manchester, United Kingdom