Study Title
Brentuximab Vedotin (Recombinant) for IV Infusion – Special Drug Use Surveillance (All-case Surveillance) “Relapsed or Refractory CD30+ Hodgkin’s Lymphoma or Anaplastic Large Cell Lymphoma” (NCT02139592)
Trial Description
The purpose of this study is to evaluate the safety of the antibody-drug conjugate or ADC brentuximab vedotin (recombinant) for IV infusion (Adcetris® IV Infusion 50 mg) in patients with relapsed/refractory CD30+ Hodgkin lymphoma or anaplastic large cell lymphoma (ALCL) in the routine clinical setting, as well as to collect efficacy information for reference.
This trial is sponsored by Takeda Pharmaceuticals. [1]
Study Data
- Condition:
- Relapsed or Refractory CD30+ Hodgkin Lymphoma
- Anaplastic Large Cell Lymphoma (ALCL)
- Interventions:
- Drugs used in this trial
- Brentuximab vedotin (Adcetris®; Seattle Genetics, Inc.)
- Drugs used in this trial
- Phase: 0
- Estimated Enrollment: 140
- Start: April 2014
- Estimated Completion: June 2017
- Last verified: May 2014
Study Schematic
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Last Editorial review: July 15, 2016
Information based on ClinicalTrials.gov (NIH/NCI) and other sources.
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