Status:
COMPLETED
Intravenous AMD3100 for Collection of Autologous Peripheral Blood Stem Cells in Patients With Lymphoma
Lead Sponsor:
Washington University School of Medicine
Conditions:
Lymphoma, Non-Hodgkin
Hodgkin Disease
Eligibility:
All Genders
18-75 years
Phase:
PHASE1
PHASE2
Brief Summary
This study will evaluate the safety and efficacy of intravenous AMD3100 added to a standard G-CSF mobilization regimen of patients undergoing autologous stem cell transplantation for lymphoma. The in...
Detailed Description
Autologous stem cell transplantation (ASCT) is indicated for patients with non-Hodgkin lymphoma (NHL) or Hodgkin lymphoma (HL) who have primary progressive disease or who relapse after a chemotherapy-...
Eligibility Criteria
Inclusion
- Age 18 to 75 years
- Diagnosis of HL or NHL eligible for autologous transplantation
- 30 days since last cycle of chemotherapy
- ECOG performance status of 0 or 1
- The patient has recovered from all acute toxic effects of prior chemotherapy
- WBC \>3.0 X 109/l
- Absolute PMN count \>1.5 X 109/l
- PLT count \>100 X 109/l
- Serum creatinine ≤ 2.2 mg/dl
- AST (SGOT), ALT (SGPT) and total bilirubin \< 2X upper limit of normal (ULN)
- Left ventricle ejection fraction \> 45% (by ECHO or MUGA scan)
- FEV1 \> 60% of predicted or DLCO \> 45% of predicted
- Negative for HIV on standard transplant workup
- Signed informed consent
- Are surgically or biologically sterile or willing to practice acceptable birth control, as follows:
- Females of child bearing potential must agree to abstain from sexual activity or to use a medically approved contraceptive measure/regimen during and for 3 months after the treatment period. Women of child bearing potential must have a negative serum or urine pregnancy test at the time of enrollment. Acceptable methods of birth control include 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
Exclusion
- A co-morbid condition which, in the view of the investigator, renders the patient at high risk for treatment complications
- Patients who have failed previous collections
- A residual acute medical condition resulting from prior chemotherapy
- Acute infection
- Fever (temp \>38C/100.4F) on the day of start of treatment
- Positive pregnancy test in female patients
- Lactating females
- Patients of child bearing potential unwilling to implement adequate birth control
- Patients whose actual body weight exceeds 150% of their ideal body weight
- History of ventricular arrhythmias
- Patients who previously received experimental therapy within 4 weeks of enrolling in this study or who are currently enrolled in another experimental study during the mobilization phase
- Patients who have deterioration of their clinical status or laboratory parameters between the time of enrollment and transplantation such that they no longer meet entry criteria may be removed from study at the discretion of the treating physician, principal investigator, or sponsor
Key Trial Info
Start Date :
November 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2013
Estimated Enrollment :
61 Patients enrolled
Trial Details
Trial ID
NCT00733824
Start Date
November 1 2008
End Date
September 1 2013
Last Update
March 9 2017
Active Locations (1)
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1
Washington University School of Medicine
St Louis, Missouri, United States, 63110