Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

leo pharma a/s - brodalumab - Ψωρίαση - Ανοσοκατασταλτικά - Το kyntheum ενδείκνυται για τη θεραπεία της μέτριας έως σοβαρής ψωρίασης πλάκας σε ενήλικες ασθενείς που είναι υποψήφιοι για συστηματική θεραπεία.

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

kyowa kirin holdings b.v. - burosumab - hypophosphatemia, familial; hypophosphatemic rickets, x-linked dominant; osteomalacia - Φάρμακα για τη θεραπεία ασθενειών των οστών - crysvita is indicated for the treatment of x-linked hypophosphataemia, in children and adolescents aged 1 to 17 years with radiographic evidence of bone disease, and in adults. crysvita is indicated for the treatment of fgf23-related hypophosphataemia in tumour-induced osteomalacia associated with phosphaturic mesenchymal tumours that cannot be curatively resected or localised in children and adolescents aged 1 to 17 years and in adults.

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

kyowa kirin ltd, united kingdom galabank business park, td1 1qh galashiels +44(0) 1896 664000 - burosumab - inj.sol (ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ) - 20mg/vial - burosumab 20mg - burosumab

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

kyowa kirin ltd, united kingdom galabank business park, td1 1qh galashiels +44(0) 1896 664000 - burosumab - inj.sol (ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ) - 10mg/vial - burosumab 10mg - burosumab

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

kyowa kirin ltd, united kingdom galabank business park, td1 1qh galashiels +44(0) 1896 664000 - burosumab - inj.sol (ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ) - 30mg/vial - burosumab 30mg - burosumab

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

ΙΦΕΤ ΑΕ 18ο χλμ. Λεωφ. Μαραθώνος,, 153 51 153 51, Παλλήνη Αττικής 210.6603400-6603522 - durvalumab - c/s.sol.in (ΠΥΚΝΟ ΔΙΑΛΥΜΑ ΓΙΑ ΠΑΡΑΣΚΕΥΗ ΔΙΑΛΥΜΑΤΟΣ ΠΡΟΣ ΕΓΧΥΣΗ) - 500mg/10ml - durvalumab 500mg - durvalumab

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

ΙΦΕΤ ΑΕ 18ο χλμ. Λεωφ. Μαραθώνος,, 153 51 153 51, Παλλήνη Αττικής 210.6603400-6603522 - durvalumab - c/s.sol.in (ΠΥΚΝΟ ΔΙΑΛΥΜΑ ΓΙΑ ΠΑΡΑΣΚΕΥΗ ΔΙΑΛΥΜΑΤΟΣ ΠΡΟΣ ΕΓΧΥΣΗ) - 120mg/2,4ml - durvalumab 120mg - durvalumab

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - emapalumab - immune system diseases - gamifant is indicated for the treatment of paediatric patients aged under 18 years with primary haemophagocytic lymphohistiocytosis (hlh).

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

astrazeneca ab - durvalumab - Καρκίνωμα, μη μικροκυτταρικός πνεύμονας - Αντινεοπλασματικοί παράγοντες - non-small cell lung cancer (nsclc)imfinzi as monotherapy is indicated for the treatment of locally advanced, unresectable non small cell lung cancer (nsclc) in adults whose tumours express pd-l1 on ≥ 1% of tumour cells and whose disease has not progressed following platinum based chemoradiation therapy (see section 5. imfinzi in combination with tremelimumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic nsclc with no sensitising egfr mutations or alk positive mutations. small cell lung cancer (sclc)imfinzi in combination with etoposide and either carboplatin or cisplatin is indicated for the first-line treatment of adults with extensive-stage small cell lung cancer (es-sclc). biliary tract cancer (btc)imfinzi in combination with gemcitabine and cisplatin is indicated for the first line treatment of adults with unresectable or metastatic biliary tract cancer (btc). hepatocellular carcinoma (hcc)imfinzi in combination with tremelimumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc).

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

astrazeneca ab - tremelimumab - carcinoma, hepatocellular - Αντινεοπλασματικοί παράγοντες - imjudo in combination with durvalumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc). imjudo in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.