Evaluation of the Use of Apixaban in Prevnetion of Thromboembolic Disease in Patients With Myeloma Trated With iMiDs

NCT02066454 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 108

Last updated 2025-08-13

No results posted yet for this study

Summary

To evaluate:

* the incidence of venous thromboembolic event (VTE)
* the incidence of hemorrhagic complications, In a population of patients with myeloma who are treated with IMiDs and require thromboprophylaxis for 6 months, using an oral anti-Xa anticoagulant, Apixaban, in a preventive scheme, 2.5 mg x2/day

Conditions

Interventions

DRUG

Apixaban

2.5mg x 2 per day during 6 months

Sponsors & Collaborators

  • Celgene

    collaborator INDUSTRY
  • University Hospital, Grenoble

    lead OTHER

Principal Investigators

  • Brigitte PEGOURIE, MD · Hospital University Grenoble

  • Gilles PERNOD, PHD · Hospital University Grenoble

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-06-05
Primary Completion
2016-07-12
Completion
2016-07-12

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02066454 on ClinicalTrials.gov