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Completed Phase 1Phase 2 Interventional Results available

A Study of Pinatuzumab Vedotin (DCDT2980S) Combined With Rituximab or Polatuzumab Vedotin (DCDS4501A) Combined With Rituximab or Obinutuzumab in Participants With Relapsed or Refractory B-Cell Non-Hodgkin's Lymphoma (NHL)

ClinicalTrials.gov ID: NCT01691898

Public ClinicalTrials.gov record NCT01691898. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 1, 2026, 9:33 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Open-Label, Multicenter, Phase II Trial Evaluating the Safety and Activity of Pinatuzumab Vedotin (DCDT2980S) in Combination With Rituximab or Polatuzumab Vedotin (DCDS4501A) in Combination With Rituximab and a Non-Randomized Phase Ib/II Evaluation of Polatuzumab Vedotin in Combination With Obinutuzumab in Patients With Relapsed or Refractory B-Cell Non-Hodgkin's Lymphoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This multicenter, open-label study will evaluate the safety and efficacy of pinatuzumab vedotin (DCDT2980S) or polatuzumab vedotin (DCDS4501A) in combination with rituximab (RTX), as well as of polatuzumab vedotin in combination with obinutuzumab in participants with relapsed or refractory (r/r) follicular lymphoma (FL) and r/r diffuse large B-cell lymphoma (DLBCL).

Study identification

NCT ID
NCT01691898
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Genentech, Inc.
Industry
Enrollment
231 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 26, 2012
Primary completion
Mar 7, 2017
Completion
Feb 6, 2019
Last update posted
Feb 20, 2020

2012 – 2019

United States locations

U.S. sites
26
U.S. states
15
U.S. cities
24
Facility City State ZIP Site status
Cedars-Sinai Medical Center Los Angeles California 90048
Stanford Cancer Center Stanford California 94305-5820
Colorado Blood Cancer Institute (CBCI) at Presbyterian/ St. Luke's Medical Center Denver Colorado 80218
Georgetown University Medical Center Lombardi Cancer Center Washington D.C. District of Columbia 20007
Florida Cancer Specialists - Fort Myers (Colonial Center Dr) Fort Myers Florida 33905
Florida Cancer Specialists; Sarasota Sarasota Florida 34232
Univ of Michigan Med School; Hematology Oncology Ann Arbor Michigan 48109
Comprehensive Cancer Centers of Nevada - Eastern Avenue Las Vegas Nevada 89169
Hematology Oncology Associates; Carol G. Simon Ctr Morristown New Jersey 07960
Regional Cancer Care Associates LLC - Morristown Morristown New Jersey 07962
Roswell Park Cancer Inst. Buffalo New York 14263
New York University Cancer Cen New York New York 10016
Oncology Hematology Care Inc Cincinnati Ohio 45242
Willamette Valley Cancer Ctr - 520 Country Club Eugene Oregon 97401-8122
Oregon Health Sciences Uni Portland Oregon 97239
Sarah Cannon Cancer Center - Tennessee Oncology, Pllc Nashville Tennessee 37203
Texas Oncology-Baylor Sammons Cancer Center Dallas Texas 75246
Cancer Care Centers of South Texas San Antonio Texas 78217
Texas Transplant Inst. San Antonio Texas 78229
Texas Oncology, P.A. - Tyler; Tyler Cancer Center Tyler Texas 75702
Fairfax N Virginia Hem/Onc PC Fairfax Virginia 22031
Oncology & Hematolgy Associates of SW Va Inc. - Roanoke Roanoke Virginia 24014
Fred Hutchinson Cancer Research Center Seattle Washington 98109
Northwest Cancer Specialists - Vancouver Vancouver Washington 98684
Yakima Valley Memorial Hospital/North Star Lodge Yakima Washington 98902
Univ of Wisconsin-Madison Madison Wisconsin 53705

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01691898, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 20, 2020 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01691898 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →