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
| Type | Name | Description |
|---|---|---|
| DRUG | plerixafor GZ316455 | Pharmaceutical form:vial Route of administration: subcutaneous injection |
| DRUG | Filgrastim | Pharmaceutical 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.