Den europeiske union - norsk - EMA (European Medicines Agency)

novartis europharm limited - ceritinib - karsinom, ikke-småcellet lunge - antineoplastiske midler - zykadia er indisert for behandling av voksne pasienter med anaplastisk lymfomkinase (alk) positiv avansert ikke-småcellet lungekreft (nsclc) som tidligere ble behandlet med crizotinib.

Den europeiske union - norsk - EMA (European Medicines Agency)

roche registration gmbh - alectinibhydroklorid - karsinom, ikke-småcellet lunge - antineoplastiske midler - alecensa som monoterapi er indisert for førstegangsbehandling av voksne pasienter med anaplastisk lymfomkinase (alk) -positive avansert ikke-småcellet lungekreft (nsclc). alecensa som monoterapi er indisert for behandling av voksne pasienter med alk‑positive avansert nsclc som tidligere er behandlet med crizotinib.

Den europeiske union - norsk - EMA (European Medicines Agency)

takeda pharma a/s - brigatinib - karsinom, ikke-småcellet lunge - antineoplastiske midler - alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase alkpositive advanced nsclc previously treated with crizotinib.

Den europeiske union - norsk - EMA (European Medicines Agency)

astrazeneca ab - durvalumab - karsinom, ikke-småcellet lunge - antineoplastiske midler - 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).

Den europeiske union - norsk - EMA (European Medicines Agency)

pfizer europe ma eeig - lorlatinib - karsinom, ikke-småcellet lunge - antineoplastic agents, protein kinase inhibitors - lorviqua as monotherapy is indicated for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. lorviqua as monotherapy is indicated for the treatment of adult patients with alk‑positive advanced nsclc whose disease has progressed after:alectinib or ceritinib as the first alk tyrosine kinase inhibitor (tki) therapy; orcrizotinib and at least one other alk tki.

Den europeiske union - norsk - EMA (European Medicines Agency)

laboratorios lesvi s.l. - dimetylfumarat - multippel sklerose, relapsing-remitting - immunsuppressive - dimethyl fumarate neuraxpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Norge - norsk - Statens legemiddelverk

abacus medicine a/s - ponatinibhydroklorid - tablett, filmdrasjert - 15 mg

Den europeiske union - norsk - EMA (European Medicines Agency)

incyte biosciences distribution b.v. - ponatinib - leukemia, myeloid; leukemia, lymphoid - antineoplastic agents, protein kinase inhibitors - iclusig is indicated in adult patients withchronic phase, accelerated phase, or blast phase chronic myeloid leukaemia (cml) who are resistant to dasatinib or nilotinib; who are intolerant to dasatinib or nilotinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the t315i mutationphiladelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) who are resistant to dasatinib; who are intolerant to dasatinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the t315i mutation. se avsnitt 4. 2 assessment of cardiovascular status prior to start of therapy and 4. 4 situations where an alternative treatment may be considered.

Norge - norsk - Statens legemiddelverk

actavis group ptc ehf (1) - imatinib - tablett, filmdrasjert - 100 mg

Norge - norsk - Statens legemiddelverk

actavis group ptc ehf (1) - imatinib - tablett, filmdrasjert - 400 mg