Non-inferiority Study of XM02 Filgrastim (Granix) and Filgrastim (Neupogen) in Combination With Plerixafor for Autologous Stem Cell Mobilization in Patients With Multiple Myeloma or Non-Hodgkin Lymphoma
Status: | Completed |
---|---|
Conditions: | Blood Cancer, Lymphoma, Lymphoma, Hematology, Hematology |
Therapuetic Areas: | Hematology, Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 7/19/2017 |
Start Date: | August 20, 2014 |
End Date: | September 18, 2016 |
A Randomized, Open Label, Non-inferiority Study of XM02 Filgrastim (Granix) and Filgrastim (Neupogen) When Administered in Combination With Plerixafor for Autologous Stem Cell Mobilization in Patients With Multiple Myeloma or Non-Hodgkin Lymphoma
This study will compare the results of stem cell mobilization using drugs called filgrastim
(Neupogen) and plerixafor with the results of stem cell mobilization using drugs called XM02
filgrastim (Granix) and plerixafor.
(Neupogen) and plerixafor with the results of stem cell mobilization using drugs called XM02
filgrastim (Granix) and plerixafor.
This study will compare the results of stem cell mobilization using drugs called filgrastim
(Neupogen) and plerixafor with the results of stem cell mobilization using drugs called XM02
filgrastim (Granix) and plerixafor. The FDA has determined that Granix is biosimilar to
Neupogen, which means that they are similar in terms of quality, safety, and efficacy;
however, Granix has not been tested in the context of stem cell mobilization to see how its
effectiveness compares to that of Neupogen
(Neupogen) and plerixafor with the results of stem cell mobilization using drugs called XM02
filgrastim (Granix) and plerixafor. The FDA has determined that Granix is biosimilar to
Neupogen, which means that they are similar in terms of quality, safety, and efficacy;
however, Granix has not been tested in the context of stem cell mobilization to see how its
effectiveness compares to that of Neupogen
Inclusion Criteria:
- At least 18 years of age
- Diagnosis of multiple myeloma or non-Hodgkin lymphoma
- Eligible for autologous transplantation
- Adequate bone marrow function as defined as:
- White Blood Cell Count ≥ 3.0x109/L
- Absolute Neutrophil Count ≥ 1.5x109/L
- Platelet Count ≥ 100x109/L
- Able to understand and willing to sign an IRB-approved informed consent document
- Surgically or biologically sterile or willing to practice acceptable birth control, as
follows:
- Women of childbearing potential must have a negative serum or urine pregnancy
test within 7 days of Day 1 of study treatment. Women of childbearing potential
must agree to abstain from sexual activity or use a medically approved
contraceptive measure/regimen during and for 3 months after the treatment period.
Acceptable methods of birth control include: barriers (condoms), oral
contraceptive, intrauterine device (IUD), transdermal/implanted or injected
contraceptives, and abstinence
- Males must agree to abstain from sexual activity or agree to utilize a medically
approved contraception method during and for 3 months after the treatment period.
Acceptable methods of birth control include: barriers (condoms), oral
contraceptive, intrauterine device (IUD), transdermal/implanted or injected
contraceptives, and abstinence
Exclusion Criteria:
- Previous autologous stem cell collection
- Known hypersensitivity to filgrastim, plerixafor, or E. coli derived products
- Pregnant or breastfeeding
We found this trial at
1
site
660 S Euclid Ave
Saint Louis, Missouri 63110
Saint Louis, Missouri 63110
(314) 362-5000
Washington University School of Medicine Washington University Physicians is the clinical practice of the School...
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