CompletedPhase 1NCT01290549
A Study of Escalating Doses of Polatuzumab Vedotin in Participants With Relapsed or Refractory B-Cell Non-Hodgkins Lymphoma and Chronic Lymphocytic Leukemia and Polatuzumab Vedotin in Combination With Rituximab in Participants With Relapsed or Refractory B-Cell Non-Hodgkins Lymphoma
Studying B-cell chronic lymphocytic leukemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Genentech, Inc.
- Principal Investigator
- Yu-Waye Chu, M.D.Genentech, Inc.
- Intervention
- Polatuzumab Vedotin(drug)
- Enrollment
- 95 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2011 – 2014
Study locations (16)
- Stanford Cancer Center, Stanford, California, United States
- Stanford Cancer Institute Pharmacy, Stanford, California, United States
- Florida Cancer Specialists; Sarasota, Sarasota, Florida, United States
- Roswell Park Cancer Inst., Buffalo, New York, United States
- Sarah Cannon Cancer Center, Germantown, Tennessee, United States
- M.D Anderson Cancer Center; Oncology, Houston, Texas, United States
- Fred Hutchinson Cancer Research Center, Seattle, Washington, United States
- Cross Cancer Institute ; Dept of Medical Oncology, Edmonton, Alberta, Canada
- British Columbia Cancer Agency, Vancouver, British Columbia, Canada
- McGill University; Sir Mortimer B Davis Jewish General Hospital; Oncology, Montreal, Quebec, Canada
- CHU Dijon - SCE Hemato, Dijon, France
- Centre Hospitalier Regional Universitaire de Lille, Lille, France
- CHU Lapeyronie, Hematologie, Montpellier, France
- Centre Hospitalier Lyon Sud; Hematolgie, Pierre-Bénite, France
- Centre Henri Becquerel; Hematologie, Rouen, France
- +1 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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