A Study of Brentuximab Vedotin in Adults With Hodgkin's Lymphoma

Takeda70 enrolled

Overview

The main aim is to check how effective BV is for treating adults with HL. Study medication will be prescribed according to the clinic's standard practice. Participants will visit the study clinic 5 times, once every 12 weeks. When study treatment has completed, a follow-up visit will be scheduled every 3 months during the first year and every 4-6 months during the next year.

This is a prospective, observational study in participants with HL who underwent or are candidates for ASCT and receiving or will receive the standard treatment of BV. This study will assess the safety profile and effectiveness of BV in pre and post-ASCT in the real-world clinical practice. The study will enroll approximately 70 participants. The data will be collected and recorded in electronic case report forms (e-CRFs) in scope of National Drug Program (NDP). All the participants will be assigned to two observational cohorts: * HL Participants: BV Salvage Pre-ASCT * HL Participants: BV Consolidation Treatment Post-ASCT This multi-center trial will be conducted in Poland. All participants will be followed up for 24 months. The overall duration of the study will be approximately 4.5 years.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Hodgkin Lymphoma

Interventions

No InterventionOTHER

This is a non-interventional study.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1\. Adult participant (aged greater than or equal to \[\>=18\] years) that underwent or are candidates for ASCT and were enrolled in BV HL NDP receiving treatment according to the Summary of Product Characteristics for Adcetris and NDP. Exclusion Criteria: 1. Currently participates or plans to participate in any interventional clinical trial. 2. Any other reason that, in the Investigator's opinion, makes the participant unsuitable to participate in this study.

Locations (13)

Uniwersytecki Szpital Kliniczny im. Jana Mikulicza-Radeckiego we Wroclawiu

Wroclaw, Dolnoslskie, Poland

RECRUITING

Outcomes

Primary Outcomes

Progression Free Survival (PFS) as Assessed by Investigator

PFS will be assessed by investigator and defined as the time from the first dose of BV post ASCT until the first occurrence of disease progression or relapse, or death for any reason. Disease progression is at least a 50 percent (%) increase in the size of lesions, or the occurrence of new lesions. It will be analyzed using Kaplan-Meier method.

Time frame: From initiation of BV treatment post-ASCT until disease progression or relapse, or death (up to 36 months)

Secondary Outcomes

Overall Survival (OS)

OS is defined as the time from initiation of therapy to death from any cause. It will be analyzed using Kaplan-Meier method.

Time frame: From initiation of BV treatment until death from any cause (up to 36 months)

Central Contacts

Takeda Contact

CONTACT

+1-877-825-3327 medinfoUS@takeda.com

Data from ClinicalTrials.gov

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