Consolidation Therapy With Brentuximab Vedotin After Allogeneic Stem Cell Transplantation for Relapsed or Refractory Hodgkin Lymphoma

  • End date
    Aug 26, 2023
  • participants needed
  • sponsor
    University of Cologne
Updated on 26 January 2021


The aim of the trial is to improve disease control after an allogeneic stem cell transplantation (alloSCT) for relapsed or refractory classical Hodgkin lymphoma (rrHL, cHL) with consolidation therapy by Brentuximab Vedotin (BV) for up to one year.

The primary objective of the trial is to show efficacy of the experimental consolidative treatment strategy. Secondary objectives are to further evaluate efficacy, show safety and feasibility and perform correlative studies.

Condition Classical Hodgkin Lymphoma
Treatment brentuximab vedotin
Clinical Study IdentifierNCT03652441
SponsorUniversity of Cologne
Last Modified on26 January 2021


Yes No Not Sure

Inclusion Criteria

Patients with relapsed/refractory cHL who receive an allogeneic stem cell transplantation
Histologically proven cHL in the most recent tumor biopsy
Absolute neutrophil count 500/mm
Age 18 years

Exclusion Criteria

Presence of nodular lymphocyte-predominant HL (NLPHL) or grey-zone lymphoma
Progressive disease as last documented response prior to alloSCT
Any peripheral neuropathy grade 2
Any other serious disease or organ dysfunction which might impair protocol treatment
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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