MK-3475 (pembrolizumab) in subjects with Classical Hodgkin Lymphoma

Mise à jour : Il y a 4 ans
Référence : EUCTR2014-004482-24

Femme et Homme

  • | Pays :
  • -
  • | Organes :
  • -
  • | Spécialités :
  • -

Extrait

To determine the safety, tolerability and Overall Response Rate (ORR) of pembrolizumab in each of the three cohorts listed below. Cohort 1: Subjects with relapsed/refractory classical Hodgkin Lymphoma who have failed to achieve a response, or progressed after auto stem cell transplant (auto-SCT) and have relapsed after treatment with or failed to respond to brentuximab vedotin. Cohort 2: Subjects with relapsed/refractory classical Hodgkin Lymphoma who were unable to achieve a complete or partial response to salvage chemotherapy and did not receive auto-SCT but have relapsed after treatment with or failed to respond to brentuximab vedotin. Cohort 3: Subjects with relapsed/refractory classical Hodgkin Lymphoma who have failed to achieve a response to or progressed after auto-SCT and have not received brentuximab vedotin. These subjects may or may not have received brentuximab vedotin as part of primary treatment or salvage therapy.


Critère d'inclusion

  • Hodgkin lymphoma