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Completed Phase 2 Interventional Results available

A Study of Brentuximab Vedotin and CHP in Frontline Treatment of PTCL With Less Than 10% CD30 Expression

ClinicalTrials.gov ID: NCT04569032

Public ClinicalTrials.gov record NCT04569032. 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 25, 2026, 10:11 AM 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 Dual-cohort, Open-label, Phase 2 Study of Brentuximab Vedotin and CHP (A+CHP) in the Frontline Treatment of Subjects With Peripheral T-cell Lymphoma (PTCL) With Less Than 10% CD30 Expression

Brief summary

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

This clinical trial will study brentuximab vedotin with CHP to find out if the drugs work for people who have certain types of peripheral T-cell lymphoma (PTCL). It will also find out what side effects occur when brentuximab vedotin and CHP are used together. A side effect is anything the drugs do besides treating cancer. CHP is a type of chemotherapy that uses three drugs (cyclophosphamide, doxorubicin, and prednisone). CHP is approved by the FDA to treat certain types of PTCL.

Study identification

NCT ID
NCT04569032
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
82 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
Nov 12, 2020 (Actual)
Primary completion
May 9, 2024 (Actual)
Completion
Jan 12, 2026 (Actual)
Last update posted
Aug 13, 2026

2020 – 2026

United States locations

U.S. sites
43
U.S. states
8
U.S. cities
28
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35233 —
University of Alabama at Birmingham Birmingham Alabama 35249 —
Stanford Cancer Center Stanford California 94305 —
Stanford Hospital and Clinics, Investigational Drug Services Stanford California 94305 —
Rocky Mountain Cancer centers, LLP Aurora Colorado 80012 —
Rocky Mountain Cancer centers, LLP Boulder Colorado 80303 —
Rocky Mountain Cancer centers, LLP Colorado Springs Colorado 80907 —
Rocky Mountain Cancer centers, LLP Denver Colorado 80218 —
Rocky Mountain Cancer centers, LLP Denver Colorado 80220 —
Rocky Mountain Cancer centers, LLP Lakewood Colorado 80228 —
Rocky Mountain Cancer centers, LLP Littleton Colorado 80120 —
Rocky Mountain Cancer centers, LLP Lone Tree Colorado 80124 —
Rocky Mountain Cancer centers, LLP Longmont Colorado 80504 —
Rocky Mountain Cancer centers, LLP Pueblo Colorado 81003 —
Rocky Mountain Cancer centers, LLP Thornton Colorado 80260 —
Tulane Cancer Center New Orleans Louisiana 70112 —
Tulane Medical Center New Orleans Louisiana 70112 —
Memorial Sloan Kettering Cancer Center David H. Koch Center for Cancer Care New York New York 10021 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Cleveland Clinic taussig Cancer Center Investigational Pharmacy Cleveland Ohio 44106 —
Cleveland Clinic, The Cleveland Ohio 44195 —
Texas Oncology - Central/South Texas Austin Texas 78705 —
Texas Oncology - Central South (Balcones Dr) Austin Texas 78731 —
Texas Oncology - Central South (James Casey) Austin Texas 78745 —
The University of Texas MD Anderson Cancer Center Houston Texas 77030 —
US Oncology Investigational Products Center (IPC) Irving Texas 75063 —
US Oncology Investigational Products Center(IPC) Irving Texas 75063 —
US Oncology lnvestigational Products Center (IPC) Irving Texas 75063 —
Texas Oncology-Northeast Texas Longview Texas 75601 —
Texas Oncology-Northeast Texas Palestine Texas 75801 —
Texas Oncology-Northeast Texas Paris Texas 75460 —
Texas Oncology-Northeast Texas Tyler Texas 75702 —
Virginia Oncology Associates Chesapeake Virginia 23320 —
Virginia Oncology Associates Hampton Virginia 23666 —
Virginia Oncology Associates Newport News Virginia 23606 —
Virginia Oncology Associates Norfolk Virginia 23502 —
VCU Massey Cancer Center-Radiation Oncology Richmond Virginia 23219 —
VCU Medical Center -InPatient Richmond Virginia 23219 —
VCU Medical Center Critical Care Hospital Richmond Virginia 23219 —
Virginia Commonwealth University Richmond Virginia 23219 —
VCU at Stony Point Richmond Virginia 23235 —
Massey Cancer Center Clinical & Translational Research Lab Richmond Virginia 23298 —
Virginia Oncology Associates Virginia Beach Virginia 23456 —

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04569032, 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 13, 2026 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04569032 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →