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Recruiting Observational

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

NCT05100056 · tracked via the Priya Life Science Poland tracker
Sponsor
Phase
Observational
Started
2022-03-08
Last updated
2026-05-27

Condition(s) studied

Hodgkin Lymphoma

Investigational drug(s) / intervention(s)

No Intervention

No Intervention: This is a non-interventional study.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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.

Primary outcome measure(s)

  • Progression Free Survival (PFS) as Assessed by Investigator — From initiation of BV treatment post-ASCT until disease progression or relapse, or death (up to 36 months)
    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.

Trial sites (13)

FacilityCityRegionStatus
Uniwersytecki Szpital Kliniczny im. Jana Mikulicza-Radeckiego we Wroclawiu Wroclaw Dolnoslskie Recruiting
Szpital Kliniczny Przemienienia Panskiego Uniwersytetu Medycznego im. Karola Marcinkowskiego w Poznaniu Poznan Greater Poland Voivodeship Recruiting
Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie Panstwowy Instytut Badawczy Oddzial w Krakowie Krakow Lesser Poland Voivodeship Recruiting
Samodzielny Publiczny Zaklad Opieki Zdrowotnej Szpital Uniwersytecki w Krakowie Krakow Lesser Poland Voivodeship Recruiting
Centrum Onkologii Ziemi Lubelskiej im. sw. Jana z Dukli Lublin Lublin Voivodeship Recruiting
NU-MED Specjalistyczny Szpital Onkologiczny Tomaszow Mazowiecki Tomaszow Mazowiecki Masovian Voivodeship Recruiting
Uniwersyteckie Centrum Kliniczne WUM Warsaw Masovian Voivodeship Recruiting
Instytut Hematologii i Transfuzjologii Warsaw Masovian Voivodeship Recruiting
Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie Panstwowy Instytut Badawczy Warsaw Masovian Voivodeship Recruiting
Uniwersyteckie Centrum Kliniczne, Gdansk Gdansk Pomeranian Voivodeship Recruiting
Samodzielny Publiczny Szpital Kliniczny im. Andrzeja Mieleckiego Slskiego Uniwersytetu Medycznego w Katowicach Katowice Slskie Recruiting
Samodzielny Publiczny Zaklad Opieki Zdrowotnej MSWiA z Warminsko - Mazurskim Centrum Onkologii w Olsztynie Olsztyn Warmian-Masurian Voivodeship Recruiting
Wojewodzkie Wielospecjalistyczne Centrum Onkologii i Traumatologii, im. M. Kopernika w Lodzi Lodz Łódź Voivodeship Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05100056 on ClinicalTrials.gov ↗ ← All trials in Poland