Unione Europea - italiano - EMA (European Medicines Agency)

janssen-cilag international n.v.    - amivantamab - carcinoma, polmone non a piccole cellule - agenti antineoplastici - rybrevant as monotherapy is indicated for treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with activating epidermal growth factor receptor (egfr) exon 20 insertion mutations, after failure of platinum-based chemotherapy.

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

janssen-cilag ag - amivantamabum - concentrato per soluzione per infusione - amivantamabum 350 mg, histidinum, histidini hydrochloridum monohydricum, saccharum, polysorbatum 80, dl-methioninum, dinatrii edetas, aqua ad iniectabile q.s. ad solutionem pro 7.0 ml corresp. natrium 17 µg. - non tumori polmonari a piccole carcinoma polmonare (nsclc) - biotechnologika

Unione Europea - italiano - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - belantamab mafodotin - mieloma multiplo - agenti antineoplastici - blenrep is indicated as monotherapy for the treatment of multiple myeloma in adult patients, who have received at least four prior therapies and whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

glaxosmithkline ag - belantamabum mafodotinum - polvere per concentrato per soluzione per infusione - praeparatio cryodesiccata: belantamabum mafodotinum 100 mg, natrii citras dihydricus, acidum citricum, trehalosum dihydricum, dinatrii edetas, polysorbatum 80, pro vitro corresp. natrium 3.15 mg. - multipli myelom - biotechnologika