First in Human Study to Determine the Safety, Tolerability and Preliminary Efficacy of an Anti-CXCR4 Antibody in Subjects With Acute Myelogenous Leukemia and Selected B-cell Cancers
Status: | Completed |
---|---|
Conditions: | Blood Cancer, Lymphoma, Hematology |
Therapuetic Areas: | Hematology, Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 5/5/2014 |
Start Date: | August 2010 |
End Date: | December 2015 |
Contact: | For participation information at a USA site use a phone number below. For site information outside the USA please email: |
Email: | Clinical.Trials@bms.com |
A Phase 1, Open-label, Multicenter Study of BMS-936564 (MDX-1338) in Subjects With Relapsed Acute Myelogenous Leukemia and Selected B-cell Malignancies
The purpose of this study is to assess the safety and tolerability of BMS-936564 (MDX-1338)
in relapsed Acute myelogenous leukemia (AML) and other selected B-cell cancers and to
determine the maximum tolerated dose (MTD) of the drug alone in relapsed/refractory AML
in relapsed Acute myelogenous leukemia (AML) and other selected B-cell cancers and to
determine the maximum tolerated dose (MTD) of the drug alone in relapsed/refractory AML
For more information regarding BMS clinical trial participation, please visit
www.BMSStudyConnect.com.
Inclusion Criteria:
A. Common to All Indications:
- Life expectancy at least 12 weeks
- ECOG Performance Status of 0-2
B. For Acute myelogenous leukemia (AML) Subjects:
- First Relapse and primary induction failure in AML (M3 excluded)
- Secondary AML subjects from myelodysplastic syndrome (MDS) or prior chemotherapy are
eligible. MDS-only subjects are not eligible
C. For Follicular Lymphoma (FL), Diffuse Large B-Cell Lymphoma (DLBCL) Subjects:
- Must be at least 4 weeks (for FL) or 2 weeks (for DLBCL) since prior cytotoxic,
biologic, monoclonal antibody, or investigational therapy
- Ability to undergo tumor biopsy pre-treatment and at end of monotherapy period
(though not mandatory for all subjects)
- Subjects must have a histologically confirmed diagnosis of relapsed or refractory
disease
D. For Chronic lymphocytic leukemia (CLL) Subjects:
- Subjects must have a histologically confirmed diagnosis of relapsed or refractory
disease
- Must be at least 4 weeks since prior cytotoxic, biologic, monoclonal antibody, or
investigational therapy, including corticosteroids
Exclusion Criteria:
A. Common to All indications:
- Prior anti-CXCR4 therapy including BMS-936564 (MDX-1338)
- Less than 3 months from prior hematopoietic stem cell transplant
- Presence of active graft versus host disease
B. For AML Subjects:
- Acute promyelocytic leukemia (M3)
- Left ventricular ejection fraction < institutional limits of normal
C. For FL, DLBCL Subjects:
- (For DLBCL): Inadequate renal function defined as creatinine clearance (by
Cockcroft-Gault formula) < 60 mL/min
- Major surgery, not related to debulking procedures, within 21 days of first dose
- Myocardial infarction within 6 months prior to screening or Class III or IV heart
failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or
electrocardiographic evidence of acute ischemia
- Myelodysplastic syndrome (MDS)
D. For CLL Subjects:
- No progression to more aggressive B-cell cancers, such as Richter's syndrome
- Major surgery within 21 days of Cycle 1, Day 1. Patients undergoing debulking
procedures and minor surgery are allowed after a recovery period, in the judgment of
the Investigator
- Myocardial infarction within 6 months prior to screening Class III or IV heart
failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or
electrocardiographic evidence of acute ischemia
We found this trial at
12
sites
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UAB Comprehensive Cancer Center One of the nation’s leading cancer research and treatment centers, the...
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Mayo Clinic Mayo Clinic's campus in Arizona provides medical care for thousands of people from...
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303 E Chicago Ave
Chicago, Illinois 60611
Chicago, Illinois 60611
(312) 503-8194
Northwestern University Feinberg School of Medicine Northwestern University Feinberg School of Medicine, founded in 1859,...
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1515 Holcombe Blvd
Houston, Texas 77030
Houston, Texas 77030
713-792-2121
University of Texas M.D. Anderson Cancer Center The mission of The University of Texas MD...
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3855 Health Sciences Dr,
La Jolla, California 92093
La Jolla, California 92093
(858) 822-6100
UC San Diego Moores Cancer Center Established in 1978, UC San Diego Moores Cancer Center...
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1441 Eastlake Ave
Los Angeles, California 90033
Los Angeles, California 90033
(323) 865-3000
U.S.C./Norris Comprehensive Cancer Center The USC Norris Comprehensive Cancer Center, located in Los Angeles, is...
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