A national phase IV study with Ipilimumab for patients with advanced malignant melanoma

Mise à jour : Il y a 4 ans
Référence : EUCTR2013-002408-15

Femme et Homme

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Extrait

•To estimate the incidence and severity of adverse reactions in adult patients treated with ipilimumab in the post-approval setting. •To describe the management of adverse reactions (eg, diarrhea, colitis, hepatitis, elevated liver enzymes, hypopituitarism, hypothyroidism, rash, neurologic syndromes) and their outcomes in ipilimumab-treated patients in the post-approval setting


Critère d'inclusion

  • Patients diagnosed with unresectable or metastatic melanoma, cutaneous, ocular, mucosal and unknown primary tumor

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