Plerixafor and G-CSF for the Mobilisation of Peripheral Blood Stem Cells for Autologous Stem Cell Transplantation in Patients with Non-Hodgkin?s Lymphoma (NHL), Hodgkin?s Disease (HD) or Multiple Myeloma (MM) ? Safety Study in a General Autologous Transplant Population - ND

Conditions: Mobilisation of peripheral blood stem cells prior autologous stem cell transplantation in patients with Non-Hodgkin?s Lymphoma (NHL), Hodgkin?s Disease (HD) or Multiple Myeloma (MM)
MedDRA version: 9.1Level: PTClassification code 10020206
MedDRA version: 9.1Level: PTClassification code 10029547
MedDRA version: 9.1Level: PTClassification code 10028228

Registration Number: EUCTR2008-000689-21-IT

Lead Sponsor: Genzyme Europe BV

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot Recruiting

Sex: All

Target Recruitment: 100

Inclusion Criteria

1. Diagnosis of MM, NHL, or HD in partial response (PR) or complete response (CR) 2. Eligible and planned for an autologous haematopoietic stem cell transplantation 3. Written informed consent 4. At least 18 years of age (inclusive) 5. Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1 6. White blood cell (WBC) count ≥2.5 × 109/L 7. Absolute neutrophil count (ANC) ≥1.5 × 109/L 8. Platelet count ≥100 × 109/L 9. Serum creatinine ≤2.2 mg/dL 10. Aspartate aminotransferase/serum glutamic oxaloacetic transaminase (AST/SGOT), alanine aminotransferase/serum glutamic pyruvic transaminase (ALT/SGPT), and total bilirubin <2.5 × upper limit of normal (ULN) 11. Adequate cardiac, renal, and pulmonary function sufficient to undergo apheresis and transplantation, i.e., eligible by institutional standards for autologous stem cell transplant 12. All patients must agree to use a highly effective method of contraception whilst on study treatment and for at least 3 months following plerixafor treatment (including both female patients of child-bearing potential and male patients with partners of child-bearing potential). Effective birth control includes: a) birth control pills, depot progesterone, or an intrauterine device plus one barrier method, or b) two barrier methods. Effective barrier methods are: male and female condoms, diaphragms, and spermicides (creams or gels that contain a chemical to kill sperm). For patients using a hormonal contraceptive method, information about any interaction of plerixafor with hormonal contraceptives is not known.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

1. History of any acute or chronic leukaemia (including myelodysplastic syndrome) 2. Prior allogeneic transplantation or more than one prior autologous transplantation 3. Failed previous CD34+ cell collection attempts (either due to insufficient yield in apheresis product, or ineligible for apheresis because of inadequate mobilisation of CD34+ cells into peripheral blood) 4. Less than 4 weeks since last anti-cancer therapy (including chemotherapy, biologic/immunologic, radiation) or less than 6 weeks if prior therapy with nitrosourea or mitomycin (for therapies with longacting agents, a treatment-free interval of at least 2 half-lives should be considered) with the exception of - Treatment with thalidomide, dexamethasone, lenalidomide (Revlimid), and/or bortezomib (Velcade) which is allowed up to 7 days prior to the first dose of G-CSF. 5. Bone marrow involvement >20% assessed based on the most recent bone marrow aspirate or biopsy 6. Treated with G-CSF or other cytokine within 14 days prior to the first dose of G-CSF for mobilisation 7. Known to be human immunodeficiency virus (HIV) positive 8. Active hepatitis B or hepatitis C 9. Acute infection (febrile, i.e., temperature >38C) within 24 hours prior to dosing or antibiotic therapy within 7 days prior to the first dose of G-CSF 10. Hypercalcaemia as evidenced by >1 mg/dL above ULN 11. Previously received investigational therapy within 4 weeks of enrolling in this protocol or currently enrolled in another investigational protocol during the mobilisation phase 12. Central nervous system involvement including brain metastases or leptomeningeal disease 13. Pregnant or nursing women 14. Electrocardiogram (ECG) or study result (exercise study, scan) indicative of cardiac ischaemia or a history of clinically significant rhythm disturbance (arrhythmias), or other conduction abnormality in the last year that in the opinion of the Investigator warrants exclusion of the subject from the trial. 15. Co-morbid condition(s), which in the opinion of the Investigator, renders the patient at high risk from treatment complications or impairs their ability to comply with the study treatment and protocol

Study & Design

Study Type: Interventional clinical trial of medicinal product

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method

Secondary Outcome Measures

Name	Time	Method

Related Trials