Secured access to vemurafenib for patients with tumors harboring BRAF genomic alterations

Mise à jour : Il y a 4 ans
Référence : EUCTR2014-001225-33

Femme et Homme

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Extrait

To explore the efficacy of vemurafenib as a single agent across diverse type of tumors guided by the presence of identified activating molecular alterations in the vemurafenib target gene, per cohort.


Critère d'inclusion

  • Patient with BRAF V600 mutation determined on the primary and/or metastatic lesion in the following pathologies:
  • . NSCLC
  • . Ovarian cancer
  • . Cholangiocarcinoma
  • . Thyroid cancer
  • . Prostatic cancer
  • . Bladder cancer
  • . Sarcoma/GIST
  • . Multiple myeloma
  • . Chronic Lymphocytic Leukemia (CLL)
  • . Hairy cell leukaemia (HCL) (this excludes Hairy Cell Leukemia variant types, marginal zone splenic lymphoma (MZL), splenic red pulp lymphoma (SRPL) patients)

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