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Terminated Phase 2 Interventional Results available

Clinical Trial of Brentuximab Vedotin in Classical Hodgkin Lymphoma

ClinicalTrials.gov ID: NCT03646123

Public ClinicalTrials.gov record NCT03646123. 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 Oct 23, 2026, 8:32 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

Multiple Part Clinical Trial of Brentuximab Vedotin in Classical Hodgkin Lymphoma Subjects

Brief summary

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

This trial will study two treatment combinations for classical Hodgkin lymphoma (cHL). This trial will find out if these two treatment combinations work to treat cHL. It will also find out what side effects occur. A side effect is anything the drug does besides treating cancer. This study will have three parts (Parts A, B, and C). The drugs used in Part A are a combination of targeted anticancer drug (brentuximab vedotin) and three chemotherapy drugs (doxorubicin, vinblastine, and dacarbazine). These four drugs are called "A+AVD." Participants will be treated with granulocyte colony stimulating factor (G-CSF) following every dose of A+AVD for 6 cycles of treatment (12 doses). Part A will look at whether the A+AVD drug combination reduces the number of participants who experience the side effect of febrile neutropenia. Febrile neutropenia is a very low white blood cell count and a fever, which can be life threatening. Parts B and C will use drug combination of brentuximab vedotin, plus nivolumab, doxorubicin, and dacarbazine. These four drugs are called "AN+AD." Parts B and C will study how well the drugs work to treat cHL and what side effects they cause.

Study identification

NCT ID
NCT03646123
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Seagen Inc.
Industry
Enrollment
255 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 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
Jan 28, 2019 (Actual)
Primary completion
Nov 7, 2022 (Actual)
Completion
Aug 23, 2024 (Actual)
Last update posted
Aug 28, 2025

2019 – 2024

United States locations

U.S. sites
55
U.S. states
19
U.S. cities
51
Facility City State ZIP Site status
Los Angeles Cancer Network / Compassionate Care Research Group Fountain Valley California 92708 —
Rocky Mountain Cancer Centers - Aurora Aurora Colorado 80012 —
University of Colorado Health Memorial Hospital Colorado Springs Colorado 80909 —
Cancer Centers of Colorado - Denver Denver Colorado 80218 —
Poudre Valley Health System (PVHS) Fort Collins Colorado 80528 —
SCL Health - St. Mary's Hospital & Medical Center Grand Junction Colorado 81501 —
Miami Cancer Institute at Baptist Health, Inc. Miami Florida 33176 —
Florida Cancer Specialists - North Region St. Petersburg Florida 33705 —
Cardinal Bernardin Cancer Center / Loyola University Medical Center Maywood Illinois 60153 —
Illinois Cancer Specialists Niles Illinois 60714 —
Illinois Cancer Care Peoria Illinois 61615 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Karmanos Cancer Institute / Wayne State University Detroit Michigan 48201 —
Henry Ford Health System Detroit Michigan 48202 —
Minnesota Oncology Hematology P.A. Edina Minnesota 55435 —
Washington University in St Louis St Louis Missouri 63110 —
New Jersey Hematology Oncology Associates, LLC Brick New Jersey 08724 —
Regional Cancer Care Associates - Freehold Freehold New Jersey 07728 —
Hackensack University Medical Center Hackensack New Jersey 07601 —
Regional Cancer Care Associates - Howell Howell Township New Jersey 07731 —
Morristown Medical Center/ Carol G. Simon Cancer Center Morristown New Jersey 07960 —
Regional Cancer Care Associates - Mount Holly Mount Holly New Jersey 08060 —
Regional Cancer Care Associates - Central Jersey Somerville New Jersey 08876 —
Regional Cancer Care Associates - Sparta Sparta New Jersey 07871 —
New York Oncology Hematology, P.C. Albany New York 12208 —
CareMount Medical Group Mount Kisco New York 10549-3412 —
Mount Sinai Medical Center New York New York 10029 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Clinical Research Alliance - Abraham Mittelman, MD, LLC Purchase New York 10577 —
Clinical Research Alliance - Morton Coleman, MD Westbury New York 11590 —
Wake Forest Baptist Medical Center / Wake Forest University Winston-Salem North Carolina 27157 —
Oncology Hematology Care Cincinnati Ohio 45242 —
University Hospitals Cleveland Medical Center Cleveland Ohio 44106 —
Cleveland Clinic, The Cleveland Ohio 44195 —
Toledo Clinic Cancer Center Toledo Ohio 43623 —
Willamette Valley Cancer Institute and Research Center Eugene Oregon 97401 —
Providence Portland Medical Center Portland Oregon 97213 —
Medical University of South Carolina/Hollings Cancer Center Charleston South Carolina 29425 —
University of Tennessee Knoxville Tennessee 37920 —
Tennessee Oncology-Nashville/Sarah Cannon Research Institute Nashville Tennessee 37203 —
Texas Oncology - Austin Midtown Austin Texas 78705 —
Texas Oncology - Medical City Dallas Dallas Texas 75230 —
Texas Oncology - Flower Mound Flower Mound Texas 75028 —
Brooke Army Medical Center Fort Sam Houston Texas 78234 —
Texas Oncology - Fort Worth 12th Avenue Fort Worth Texas 76104 —
MD Anderson Cancer Center / University of Texas Houston Texas 77030-4095 —
Texas Oncology - San Antonio Medical Center San Antonio Texas 78240 —
Texas Oncology - Northeast Texas Tyler Texas 75702 —
Huntsman Cancer Institute/University of Utah Salt Lake City Utah 84112 —
Virginia Cancer Specialists, PC Fairfax Virginia 22031 —
Oncology and Hematology Assoc of SW VA DBA Blue Ridge Cancer Care Salem Virginia 24153 —
Kadlec Clinic Hematology and Oncology Kennewick Washington 99336 —
Vista Oncology Inc PS Olympia Washington 98506 —
Seattle Cancer Care Alliance / University of Washington Seattle Washington 98109-1023 —

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 21 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03646123, 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 Aug 28, 2025 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03646123 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →