Study of Intravenously Administered SNS-032 in Patients With Advanced B-lymphoid Malignancies
Completed · Phase 1
Conditions studied: B-lymphoid Malignancies, Chronic Lymphocytic Leukemia, Mantle Cell Lymphoma, Multiple Myeloma
In brief
The purpose of this study is to assess the safety and tolerability of escalating doses of SNS-032, given in 3 weekly administrations per cycle and to identify a recommended Phase 2 dose.
Key facts
- Study ID
- NCT00446342
- Run by
- Sunesis Pharmaceuticals
- People needed
- 21
- Starts
- 2007-02-01
- Expected to finish
- 2009-03-01
- Last updated by the study team
- 2017-04-11
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Cytologically or histologically confirmed chronic lymphocytic leukemia (CLL), mantle cell lymphoma (MCL), or multiple myeloma (MM).
- Evidence of relapsed disease
- Measurable disease
- Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1
You may not qualify if…
- Prior treatment with SNS-032 injection (previously known as BMS-387032)
- Pregnant or breastfeeding
- Unwilling to use an approved, effective means of contraception according to the study site's standards
- Use of therapeutic anticoagulation agents
- Prior allogeneic bone marrow transplantation
- Prior chemotherapy, monoclonal antibodies, investigational agents, or radiation therapy within 21 days before the first dose; nitrosoureas and mitomycin are not permitted for at least 42 days before the first dose.
- Prior pelvic radiation therapy or radiation to > 25% of bone marrow reserve
- Any other medical, psychological, or social condition that would contraindicate the patient's participation in the clinical study due to safety concerns or compliance with clinical study procedures
- Please note: There are additional inclusion/exclusion criteria for this study. Please contact the study center for additional information and to determine if the patient meets all study criteria.
Where it is running
- City of Hope — Duarte, California, United States
- Stanford Cancer Center — Stanford, California, United States
- Winship Cancer Institute at Emory University — Atlanta, Georgia, United States
- Greenebaum Cancer Center, University of Maryland — Baltimore, Maryland, United States
- Hackensack University Medical Center at the Cancer Center — Hackensack, New Jersey, United States
- MD Anderson Cancer Center, University of Texas — Houston, Texas, United States
Full record on ClinicalTrials.gov
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