ClinicalTrials.gov record
Completed Phase 1Phase 2 Interventional Results available

A Phase Ib/II Study Investigating the Safety, Tolerability, Pharmacokinetics, and Efficacy of Mosunetuzumab (BTCT4465A) in Combination With CHOP or CHP-Polatuzumab Vedotin in Participants With B-Cell Non-Hodgkin Lymphoma

ClinicalTrials.gov ID: NCT03677141

Public ClinicalTrials.gov record NCT03677141. 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 May 3, 2026, 5:23 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 Phase Ib/II, Open-Label, Multicenter, Randomized, Controlled Study Investigating the Safety, Tolerability, Pharmacokinetics, and Efficacy of Mosunetuzumab (BTCT4465A) in Combination With CHOP or CHP-Polatuzumab Vedotin in Patients With B-Cell Non-Hodgkin Lymphoma

Study identification

NCT ID
NCT03677141
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
117 participants

Conditions and interventions

Interventions

  • Cyclophosphamide Drug
  • Doxorubicin Drug
  • Mosunetuzumab Drug
  • Polatuzumab Vedotin Drug
  • Prednisone Drug
  • Rituxumab Drug
  • Tocilizumab Drug
  • Vincristine Drug

Drug

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
Mar 7, 2019
Primary completion
Oct 11, 2023
Completion
Oct 11, 2023
Last update posted
Dec 17, 2024

2019 – 2023

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
University of Alabama Birmingham Birmingham Alabama 35233
Banner MD Anderson Cancer Center Gilbert Arizona 85234
University of California; Moores Cancer Center La Jolla California 92093
University of California, Los Angeles (UCLA) - Hematology/Oncology Santa Monica Santa Monica California 90404-2023
Georgetown University Medical Center Washington D.C. District of Columbia 20007
University of Miami Miller School of Medicine Miami Florida 33136
University of Kansas Cancer Center Westwood Kansas 66205
Dana-Farber Cancer Institute Boston Massachusetts 02215
University of Michigan Ann Arbor Michigan 48109
Mayo Clinic Cancer Center Rochester Minnesota 55905
Rhode Island Hospital Providence Rhode Island 02903-4923
Vanderbilt University Medical Center Nashville Tennessee 37232
The University of Texas MD Anderson Cancer Center Houston Texas 77030-4009
Scott and White Hospital; Cancer Center Temple Texas 76508
Medical College of Wisconsin, Inc. Milwaukee Wisconsin 53226-3596

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 26 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03677141, 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 Dec 17, 2024 · Synced May 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03677141 live on ClinicalTrials.gov.

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