A Study of Brentuximab Vedotin and CHP in Frontline Treatment of PTCL With Less Than 10% CD30 Expression - Trial NCT04569032
Access comprehensive clinical trial information for NCT04569032 through Pure Global AI's free database. This Phase 2 trial is sponsored by Seagen Inc. and is currently Recruiting. The study focuses on Peripheral T-cell Lymphoma. Target enrollment is 80 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
Sponsor & Location
Seagen Inc.
Timeline & Enrollment
Phase 2
Nov 12, 2020
Dec 31, 2023
Primary Outcome
Objective response rate (ORR) per blinded independent central review (BICR) using Revised Response Criteria for Malignant Lymphoma criteria (Cheson 2007)
Summary
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.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT04569032
Non-Device Trial

