Clinical Trials Directory

Trials / Completed

CompletedNCT02221479

Plerixafor Plus Granulocyte Colony-stimulating Factor (G-CSF) For Mobilization And Collection Of Peripheral Hematopoietic Stem Cells In Japanese Participants With Multiple Myeloma

A Randomized, Open-label, Two-arm Parallel Group, Comparative Study for Assessing the Clinical Benefit of Subcutaneous Injection of Plerixafor Plus G-CSF for Mobilization and Collection of Peripheral Hematopoietic Stem Cells in Japanese Patients With Multiple Myeloma

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
14 (actual)
Sponsor
Genzyme, a Sanofi Company · Industry
Sex
All
Age
20 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Primary Objective: To determine if Multi Myeloma (MM) patients mobilized with granulocyte colony-stimulating factor (G-CSF) plus plerixafor 240 μg/kg are more likely to achieve a target number of greater than or equal to 6 x 10\^6 cluster of differentiation (CD) 34+ cells/kg in 2 or fewer days of apheresis than MM patients mobilized with G-CSF alone. Secondary Objectives: * To evaluate the safety of G-CSF plus plerixafor arm compared to G-CSF arm in MM patients. * To compare the 2 treatment arms with respect to the number of participants who achieved a minimum of 2 x 10\^6 CD34+ cells/kg in 4 or fewer days of apheresis. * To compare the 2 treatment arms with respect to the number of days of apheresis required to reach the target of greater than or equal to 6 x 10\^6 CD34+ cells/kg.

Detailed description

Total study duration for a participant can be approximately up to 68 days.

Conditions

Interventions

TypeNameDescription
DRUGplerixafor GZ316455Pharmaceutical form:vial Route of administration: subcutaneous injection
DRUGFilgrastimPharmaceutical form:vial Route of administration: subcutaneous injection

Timeline

Start date
2014-10-01
Primary completion
2015-07-01
Completion
2015-07-01
First posted
2014-08-20
Last updated
2015-08-04

Locations

5 sites across 1 country: Japan

Source: ClinicalTrials.gov record NCT02221479. Inclusion in this directory is not an endorsement.