Phase 4 Study of Brentuximab Vedotin in Patients With Relapsed or Refractory Systemic Anaplastic Large Cell Lymphoma

Update Il y a 4 ans
Reference: EUCTR2012-004128-39

Woman and Man

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Extract

To assess the antitumor efficacy of single-agent brentuximab vedotin (1.8 mg/kg administered intravenously every 3 weeks) as measured by the overall objective response rate (ORR) in patients with relapsed or refractory sALCL following at least 1 multiagent chemotherapy (CHOP or equivalent multiagent chemotherapy regimens with curative intent)


Inclusion criteria

  • Relapsed or Refractory Systemic Anaplastic Large Cell Lymphoma