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Spots Global Cancer Trial Database for 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

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Trial Identification

Brief Title: 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

Official Title: An Open-Label, Multicenter, Phase I Trial of the Safety and Pharmacokinetics Of Escalating Doses of DCDS4501A in Patients With Relapsed or Refractory B-Cell Non-Hodgkins Lymphoma and Chronic Lymphocytic Leukemia and DCDS4501A in Combination With Rituximab in Patients With Relapsed or Refractory B-Cell Non-Hodgkins Lymphoma

Study ID: NCT01290549

Study Description

Brief Summary: This is a Phase I, multicenter, open-label, dose-escalation study of polatuzumab vedotin administered as a single agent by intravenous (IV) infusion to participants with relapsed or refractory hematologic malignancies. In Phase Ib, participants will receive polatuzumab vedotin in combination with rituximab.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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 Benite, , France

Centre Henri Becquerel; Hematologie, Rouen, , France

Academisch Medisch Centrum; Hematologie, Amsterdam, , Netherlands

Contact Details

Name: Yu-Waye Chu, M.D.

Affiliation: Genentech, Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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