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

sanofi-aventis (suisse) sa - dupilumabum - soluzione iniettabile in siringa pre-riempita con sistema di sicurezza - dupilumabum 300 mg, histidinum, histidini hydrochloridum monohydricum, arginini hydrochloridum, natrii acetas trihydricus, acidum aceticum glaciale, polysorbatum 80, saccharum, aqua ad iniectabile q.s. ad solutionem pro 2 ml corresp. natrium 0.45 mg. - dermatite atopique modérée à sévère, asthme, polypose naso-sinusienne, prurigo nodularis et œsophagite à éosinophiles - biotechnologika

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

sanofi-aventis (suisse) sa - dupilumabum - soluzione iniettabile en seringue préremplie - dupilumabum 300 mg, histidinum, histidini hydrochloridum monohydricum, arginini hydrochloridum, natrii acetas trihydricus, acidum aceticum glaciale, polysorbatum 80, saccharum, aqua ad iniectabile q.s. ad solutionem pro 2 ml. - dermatite atopique modérée à sévère chez l’adulte, l'asthme à partir de 12 ans et la polypose naso-sinusienne - biotechnologika

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

sanofi-aventis (suisse) sa - dupilumabum - soluzione iniettabile in siringa pre-riempita con sistema di sicurezza - dupilumabum 200 mg, histidinum, histidini hydrochloridum monohydricum, arginini hydrochloridum, natrii acetas trihydricus, acidum aceticum glaciale, saccharum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 1.14 ml corresp. natrium 0.25 mg. - dermatite atopique modérée à sévère, asthme, polypose naso-sinusienne, prurigo nodularis et œsophagite à éosinophiles - biotechnologika

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

sanofi-aventis (suisse) sa - dupilumabum - soluzione iniettabile in penna pre-riempita - dupilumabum 200 mg, histidinum, histidini hydrochloridum monohydricum, arginini hydrochloridum, natrii acetas trihydricus, acidum aceticum glaciale, saccharum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 1.14 ml corresp. natrium 0.25 mg. - dermatite atopique modérée à sévère, asthme, polypose naso-sinusienne, prurigo nodularis et œsophagite à éosinophiles. - biotechnologika

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

sanofi-aventis (suisse) sa - dupilumabum - soluzione iniettabile in penna pre-riempita - dupilumabum 300 mg, histidinum, histidini hydrochloridum monohydricum, arginini hydrochloridum, natrii acetas trihydricus, acidum aceticum glaciale, saccharum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 2 ml corresp. natrium 0.45 mg. - dermatite atopique modérée à sévère, asthme, polypose naso-sinusienne, prurigo nodularis et œsophagite à éosinophiles. - biotechnologika

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

sanofi-aventis (suisse) sa - dupilumabum - soluzione iniettabile in siringa pre-riempita con sistema di sicurezza - dupilumabum 100 mg, histidinum, histidini hydrochloridum monohydricum, natrii acetas trihydricus, acidum aceticum glaciale, arginini hydrochloridum, saccharum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 0.67 ml, natrium 0.15 mg. - dermatite atopique modérée à sévère, asthme, polypose naso-sinusienne, prurigo nodularis et œsophagite à éosinophiles - biotechnologika

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

abacus medicine a/s - nivolumab - nivolumab

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

gekofar s.r.l. - nivolumab - nivolumab

Unione Europea - italiano - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - ipilimumab - melanoma; carcinoma, renal cell; carcinoma, non-small-cell lung; mesothelioma, malignant; colorectal neoplasms - agenti antineoplastici - melanomayervoy as monotherapy or combination with nivolumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older (see section 4.  yervoy in combination with nivolumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults. relative to nivolumab monotherapy, an increase in progression-free survival (pfs) and overall survival (os) for the combination of nivolumab with ipilimumab is established only in patients with low tumour pd-l1 expression (see sections 4. 4 e 5. renal cell carcinoma (rcc)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with intermediate/poor-risk advanced renal cell carcinoma (see section 5. non-small cell lung cancer (nsclc)yervoy in combination with nivolumab and 2 cycles of platinum-based chemotherapy is indicated for the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising egfr mutation or alk translocation. malignant pleural mesothelioma (mpm)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. mismatch repair deficient (dmmr) or microsatellite instability-high (msi-h) colorectal cancer (crc)yervoy in combination with nivolumab is indicated for the treatment of adult patients with mismatch repair deficient or microsatellite instability-high metastatic colorectal cancer after prior fluoropyrimidine based combination chemotherapy (see section 5. oesophageal squamous cell carcinoma (oscc)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%.

Unione Europea - italiano - EMA (European Medicines Agency)

ipsen pharma - cabozantinib (s)-malate - carcinoma, renal cell; carcinomas, hepatocellular - agenti antineoplastici - renal cell carcinoma (rcc)cabometyx is indicated as monotherapy for the treatment of advanced renal cell carcinoma (rcc):in treatment-naïve adults with intermediate or poor risk,in adults following prior vascular endothelial growth factor (vegf)-targeted therapy. cabometyx, in combination with nivolumab, is indicated for the first-line treatment of advanced renal cell carcinoma in adults. hepatocellular carcinoma (hcc)cabometyx is indicated as monotherapy for the treatment of hepatocellular carcinoma (hcc) in adults who have previously been treated with sorafenib.