Unión Europea - español - EMA (European Medicines Agency)

astrazeneca ab - durvalumab - carcinoma, pulmón no microcítico - agentes antineoplásicos - 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).

Chile - español - ISPC (Instituto de Salud Pública de Chile)

astrazeneca s.a. - durvalumab - sin formulas

Chile - español - ISPC (Instituto de Salud Pública de Chile)

astrazeneca s.a. - durvalumab - sin formulas

Perú - español - DIGEMID (Dirección General de Medicamentos, Insumos y Drogas)

astrazeneca peru s.a. - droguerÍa - durvalumab - concentrado para solución para perfusión - 50 mg/ml - por mililitro 1.00 - - durvalumab

Ecuador - español - Agencia Nacional de Regulación, Control y Vigilancia Sanitaria

astrazeneca ab suecia - durvalumab 50mg/ml - concentrado para solucion para perfusion - durvalumab 50mg/ml

Estados Unidos - español - Ecolab

ecolab deutschland gmbh -

Perú - español - DIGEMID (Dirección General de Medicamentos, Insumos y Drogas)

durvalumab - concentrado para solución para perfusión - 50 mg/ml

Unión Europea - español - EMA (European Medicines Agency)

astrazeneca ab - tremelimumab - carcinoma, hepatocellular - agentes antineoplásicos - 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.

Unión Europea - español - EMA (European Medicines Agency)

astrazeneca ab - tremelimumab - carcinoma, pulmón no microcítico - agentes antineoplásicos - tremelimumab astrazeneca 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.

Unión Europea - español - EMA (European Medicines Agency)

tigenix n.v. - células cartilaginosas autólogas caracterizadas expandidas ex vivo que expresan proteínas marcadoras específicas - enfermedades del cartílago - otras drogas para trastornos del sistema musculoesquelético - reparación de defectos solo sintomático cartílago del cóndilo femoral de la rodilla (grado iii o iv de sociedad internacional de reparación cartílago [icrs]) en adultos. concomitante asintomáticos lesiones del cartílago (icr grado i o ii) puede estar presente. demostración de la eficacia se basa en un ensayo aleatorizado y controlado para evaluar la eficacia de chondrocelect en pacientes con lesiones entre 1 y 5 cm2.