CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 82 enrolled
Drug / intervention
brentuximab vedotin +3 moredrug
Likely dose
brentuximab vedotin 1.8 mg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04569032
NCT04569032Phase 2Completed

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

Seagen, a wholly owned subsidiary of Pfizer·interventional·Posted Sep 29, 2020·Updated Feb 18, 2026

In Brief

A Phase 2 clinical trial evaluating brentuximab vedotin, cyclophosphamide, and 2 other interventions for Peripheral T-cell Lymphoma. Completed, enrolled 82 participants across 63 sites in 5 countries.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance, Italy, Spain, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
202120222023202420252026
First PostedSep 29, 2020
Enrollment StartNov 12, 2020
Primary CompletionMay 9, 2024
Study CompletionJan 12, 2026
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 5.8 years ago

Interventions

brentuximab vedotindrug

1.8 mg/kg administered intravenously (IV; into the vein) on Day 1 of each 21 -day cycle

cyclophosphamidedrug

750 mg/m\^2 administered intravenously (IV; into the vein) on Day 1 of each 21 -day cycle

doxorubicindrug

50 mg/m\^2 administered intravenously (IV; into the vein) on Day 1 of each 21 -day cycle

prednisonedrug

100 mg daily administered orally on Days 1-5 of each cycle