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Clinical Trials/NCT01738373
NCT01738373
Completed
Not Applicable

Investigator Centers Will Be All French Hematology Centers Performing Autologous Transplantation and Prescribing Mozobil in Hematopoietic Stem Cell Mobilization Willing to Participate In This Study

Genzyme, a Sanofi Company0 sites262 target enrollmentDecember 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bone Marrow / Autologous Transplants
Sponsor
Genzyme, a Sanofi Company
Enrollment
262
Primary Endpoint
Duration of treatment
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The aim of this registry is to provide information, in day-to-day practice, on Plerixafor prescription modalities in France, over a 13-month period in order to address the health authorities' request.

Registry
clinicaltrials.gov
Start Date
December 2011
End Date
November 2012
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Genzyme, a Sanofi Company
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients treated with Plerixafor for autologous transplantation between November 2011 and November 2012
  • Patients who have been informed and who have given their written consent for the access to their medical file

Exclusion Criteria

  • Patients already included in a Plerixafor ongoing clinical trial.

Outcomes

Primary Outcomes

Duration of treatment

Time Frame: 13 months

Associated treatments

Time Frame: 13 months

The characteristics of the patients who received treatment

Time Frame: 13 months

Dosage of treatment

Time Frame: 13 months

Number of CD34+ cells collected following treatment

Time Frame: 13 months

Number of patients with the existence of one or more predictive factors of poor mobilisation

Time Frame: 13 months

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