CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 131 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/NCT01716806
NCT01716806Phase 2Completed

A Phase 2 Open-label Study of Brentuximab Vedotin in Front-line Therapy of Hodgkin Lymphoma (HL) an dCD30-expressing Peripheral T-cell Lymphoma (PTCL) in Older Patients or Patients With Significant Comorbidities Ineligible for Standard Chemotherapy

Seagen Inc.·interventional·Posted Oct 30, 2012·Updated Jun 11, 2024

In Brief

A Phase 2 clinical trial evaluating brentuximab vedotin, bendamustine, and 2 other interventions for Hodgkin Disease and Peripheral T Cell Lymphoma. Completed, enrolled 131 participants across 54 sites in 2 countries.

Detailed Summary

This trial will study brentuximab vedotin to find out whether it is an effective treatment for Hodgkin lymphoma (HL) and peripheral T-cell lymphoma (PTCL). Participants in this study will be older or will have other conditions that make them unable to have standard chemotherapy treatment. The study will look at brentuximab vedotin alone and combined with other drugs.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, United States

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedOct 30, 2012
Enrollment StartOct 31, 2012
Primary CompletionApr 7, 2023
Study CompletionSep 12, 2023
TodayJul 2, 2026
Enrollment to primary: 10.4 yearsPosted 13.7 years ago

Interventions

brentuximab vedotindrug

1.8 mg/kg every 3 weeks by IV infusion

bendamustinedrug

70 mg/m\^2 by IV infusion on Days 1 and 2 of 3-week cycle

dacarbazinedrug

375 mg/m\^2 every 3 weeks by IV infusion

nivolumabdrug

3 mg/kg every 3 weeks by IV infusion