A Study of Brentuximab Vedotin and CHP in Frontline Treatment of PTCL With Less Than 10% CD30 Expression
- Disease/Condition
- Peripheral T-cell Lymphoma
- Drug/Device/Intervention
- brentuximab vedotin
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Seagen Inc.
- Location
- Birmingham,Stanford,Aurora,Aurora,Washington,Niles,New Orleans,New Orleans,Ann Arbor,New York,Cleveland,Fairfield,Knoxville,Amarillo,Austin,Fort Worth,Houston,Longview,Richmond,Virginia Beach,Cedex 9,, France,Italy,Spain,United Kingdom,United States of America
- Phase
- Phase 2
- Start date
- Nov 12, 2020
- End date
- Dec 31, 2023
- Enrollment
- 80 participants
Objective response rate (ORR) per blinded independent central review (BICR) using Revised Response Criteria for Malignant Lymphoma criteria (Cheson 2007)
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.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT04569032
- Type
- Non-Device Trial
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.