Study of Brentuximab Vedotin (SGN-35) in Pediatric Participants With Relapsed or Refractory (r/r) Systemic Anaplastic Large-Cell Lymphoma or Hodgkin Lymphoma

Update Il y a 5 ans
Reference: NCT01492088

Woman and Man

Extract

The purpose of this study is to assess the safety and pharmacokinetics, and determine the pediatric maximum tolerated dose and/or or recommended phase 2 dose of brentuximab vedotin.


Inclusion criteria

  • relapsed or refractory Hodgkin Lymphoma ,Relapsed or Refractory Anaplastic Large-cell Lymphoma


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