MedPath

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 Disorder
Bleeding During/Following Surgery
Interventions
Procedure: standard therapy
Drug: activated recombinant human factor VII
Drug: 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
Read More
Exclusion Criteria
  • Known or suspected allergy to trial product
  • Participation in other trials with unapproved drugs or trials with equal or similar objective
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Placebostandard therapy-
Low dosestandard therapy-
Low doseactivated recombinant human factor VII-
High doseactivated recombinant human factor VII-
Medium doseactivated recombinant human factor VII-
High dosestandard therapy-
Placeboplacebo-
Medium dosestandard therapy-
Primary Outcome Measures
NameTimeMethod
Effect on bleeding, defined as change in bleeding score
Secondary Outcome Measures
NameTimeMethod
Bleeding evaluation
Transfusion requirements
Adverse events

Trial Locations

Locations (1)

Novo Nordisk Investigational Site

🇬🇧

Manchester, United Kingdom

© Copyright 2025. All Rights Reserved by MedPath