Evaluation of Plerixafor Plus G-CSF to Mobilize and Collect 5×10^6CD34+ Cells/kg in Non-Hodgkin's Lymphoma (NHL) Patients for Autologous Transplantation

• Status: Completed
• Trial end date: 2014-11-01
• Target enrollment: 0
• Participant gender: All

Summary

The study is to determine if NHL patients mobilized with G-CSF (10 µg/kg/day [GRAN® only]) plus 0.24 mg/kg/day of plerixafor are more likely to achieve a target number of ≥5 × 10^6 CD34+ cells/kg in 4 or fewer days of apheresis than NHL patients mobilized with G-CSF plus placebo.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Sanofi
• Treatments: JM 3100; Lenograstim; Plerixafor; Sargramostim

Criteria

Inclusion Criteria:

• Has a biopsy-confirmed diagnosis of NHL

• Is in first or second complete remission or partial remission, defined for the purpose of this study as complete or partial response following first- or second-line therapy

• Treatment with an autologous peripheral HSC transplant is planned and the patient is eligible for autologous transplantation

• Has an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1

• Has recovered from all acute toxic effects of prior chemotherapy or other cancer treatment.

• Has an actual body weight <175% of their ideal body weight (IBW)

• The patient agrees to use a highly effective method of contraception from Day 1 through ≥3 months following plerixafor treatment.

Exclusion Criteria:

• Concurrent serious illness and pathological conditions

• Has undergone previous HSC collections or collection attempt

• Has had any autologous or allogeneic HSC transplant

• Has active central nervous system (CNS) involvement

• Bone marrow lymphoma cells involvement >20%, as assessed by bone marrow biopsy within 4 months before signing the ICF

• Has received radiation therapy to the pelvis

• Has a diagnosis of all leukemias including any type of CLL

• Active infection

• Pregnant or nursing

• Anticipated post-transplant chemotherapy and/or radiation therapy below the diaphragm

• Received any prior radio-immunotherapy

• Prior 1,3-bis(2-chloroethyl)-1-nitroso-urea (BCNU) within 6 weeks prior to first dose of G-CSF

• Prior cancer therapy, other investigational therapy within 4 weeks prior to first dose of G-CSF

• Prior granulocyte/macrophage-colony stimulating factor (GM-CSF) or pegfilgrastim within 3 weeks prior to the first dose of G-CSF

• Prior G-CSF within 2 weeks prior to the first dose of G-CSF

• Inadequate organ funtion evidenced by unacceptable laboratory result