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NCT02139592 (CLINICAL TRIAL / BRENTUXIMAB VEDOTIN / SGN-035 / ADCETRIS®)

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:
  • Phase: 0
  • Estimated Enrollment: 140
  • Start: April 2014
  • Estimated Completion: June 2017
  • Last verified: May 2014

Study Schematic

NCT02139592 (CLINICAL TRIAL / BRENTUXIMAB VEDOTIN / SGN-035 / ADCETRIS®)

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Last Editorial review: July 15, 2016
Information based on ClinicalTrials.gov (NIH/NCI) and other sources.

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