Imfinzi Unia Europejska - polski - EMA (European Medicines Agency)

imfinzi

astrazeneca ab - durvalumab - rak, niedrobnokomórkowe płuca - Środki przeciwnowotworowe - 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).

Poteligeo Unia Europejska - polski - EMA (European Medicines Agency)

poteligeo

kyowa kirin holdings b.v. - mogamulizumab - sezary syndrome; mycosis fungoides - Środki przeciwnowotworowe - poteligeo jest wskazany do leczenia dorosłych pacjentów z kandydoza jamy ustnej (mf) lub zespół sézary (ss), które uzyskały co najmniej jeden przed systemowej terapii.

Libtayo Unia Europejska - polski - EMA (European Medicines Agency)

libtayo

regeneron ireland designated activity company (dac) - cemiplimab - rak, płaskonabłonkowy - Środki przeciwnowotworowe - cutaneous squamous cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with metastatic or locally advanced cutaneous squamous cell carcinoma (mcscc or lacscc) who are not candidates for curative surgery or curative radiation. basal cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic basal cell carcinoma (labcc or mbcc) who have progressed on or are intolerant to a hedgehog pathway inhibitor (hhi). non-small cell lung cancerlibtayo as monotherapy is indicated for the first-line treatment of adult patients with non-small cell lung cancer (nsclc) expressing pd-l1 (in ≥ 50% tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. libtayo in combination with platinum‐based chemotherapy is indicated for the first‐line treatment of adult patients with nsclc expressing pd-l1 (in ≥ 1% of tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. cervical cancerlibtayo as monotherapy is indicated for the treatment of adult patients with recurrent or metastatic cervical cancer and disease progression on or after platinum-based chemotherapy.

Masiviera Unia Europejska - polski - EMA (European Medicines Agency)

masiviera

ab science - masitinib - nowotwory trzustki - inhibitory białka kinazy - leczenie działać lokalnie-postępowym lub przerzutowym rakiem trzustki .

Masican Unia Europejska - polski - EMA (European Medicines Agency)

masican

masitinib - guzy stromal żołądkowo-jelitowe - inhibitory białka kinazy - leczenie działać i/lub rozsiana złym стромальной nowotworów przewodu pokarmowego (gist).

Vanflyta Unia Europejska - polski - EMA (European Medicines Agency)

vanflyta

daiichi sankyo europe gmbh - quizartinib дигидрохлорид - białaczka, szpikowe, ostre - Środki przeciwnowotworowe - leczenie ostrej białaczki szpikowej.

Piqray Unia Europejska - polski - EMA (European Medicines Agency)

piqray

novartis europharm limited  - alpelisib - nowotwory piersi - Środki przeciwnowotworowe - piqray podaje się w połączeniu z fulwestrant do leczenia kobiet po menopauzie i mężczyzn, z hormonem receptorów (or)-pozytywny, ludzki эпидермическое 2 receptor czynnika wzrostu (her2)-ujemny, lokalnie-postępowym lub przerzutowym rakiem piersi z mutacją pik3ca po progresji choroby po terapii hormonalnej w monoterapii (patrz punkt 5.

Sarclisa Unia Europejska - polski - EMA (European Medicines Agency)

sarclisa

sanofi winthrop industrie - isatuximab - szpiczak mnogi - Środki przeciwnowotworowe - sarclisa is indicated: in combination with pomalidomide and dexamethasone, for the treatment of adult patients with relapsed and refractory multiple myeloma (mm) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor (pi) and have demonstrated disease progression on the last therapy. in combination with carfilzomib and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least one prior therapy (see section 5.

Blenrep Unia Europejska - polski - EMA (European Medicines Agency)

blenrep

glaxosmithkline (ireland) limited - belantamab mafodotin - szpiczak mnogi - Środki przeciwnowotworowe - 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.

Turalio Unia Europejska - polski - EMA (European Medicines Agency)

turalio

daiichi sankyo europe gmbh - pexidartinib - giant cell tumor of tendon sheath; synovitis, pigmented villonodular - Środki przeciwnowotworowe - treatment of tenosynovial giant cell tumour.