Evropska unija - slovenščina - EMA (European Medicines Agency)

astrazeneca ab - durvalumab - karcinom, pljučni pljuč - antineoplastična sredstva - 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).

Evropska unija - slovenščina - EMA (European Medicines Agency)

akcea therapeutics ireland limited - inotersen natrijev - amiloidoza - druga zdravila na živčnem sistemu - zdravljenje faza 1 in faza 2 polyneuropathy pri odraslih bolnikih z dedno transthyretin amyloidosis (hattr).

Evropska unija - slovenščina - EMA (European Medicines Agency)

orion corporation - ropinirole hidroklorid - dopaminergičnih agenti, agonisti dopamina - psi - indukcijsko bruhanja pri psih.

Evropska unija - slovenščina - EMA (European Medicines Agency)

novartis europharm limited  - voretigene neparvovec - leber congenital amaurosis; retinitis pigmentosa - other ophthalmologicals - luxturna je indiciran za zdravljenje odraslih in pediatričnih bolnikih z izgubo vida zaradi dedne očesne mrežnice distrofija, ki jih povzročajo potrdili biallelic rpe65 mutacije in ki imajo dovolj preživetja celic mrežnice.

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

virbac -

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

intervet international -

Evropska unija - slovenščina - EMA (European Medicines Agency)

akcea therapeutics ireland limited - volanesorsen natrijev - hiperlipoproteinemija tipa i - drugih lipidov spreminjanje agenti - waylivra je indicirano kot dodatek k dieti pri odraslih bolnikih z gensko potrdili družinsko chylomicronemia sindrom (fcs) in na visoko tveganje za pankreatitisa, v kateri je odziv na dieto in trigliceridov znižanje terapija je bila neustrezna.

Evropska unija - slovenščina - EMA (European Medicines Agency)

celgene europe bv - azacitidin - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - antineoplastična sredstva - azacitidine celgene is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (hsct) with:intermediate 2 and high-risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss),chronic myelomonocytic leukaemia (cmml) with 10 29 % marrow blasts without myeloproliferative disorder,acute myeloid leukaemia (aml) with 20 30 % blasts and multi-lineage dysplasia, according to world health organisation (who) classification,aml with >30% marrow blasts according to the who classification.

Evropska unija - slovenščina - EMA (European Medicines Agency)

novartis europharm limited  - onasemnogene abeparvovec - mišična atrofija, hrbtenica - druga zdravila za motnje mišično-skeletnega sistema - zolgensma je primerna za zdravljenje:pri bolnikih z 5q hrbtenice mišična atrofija (sma) z dvo-allelic mutacije v smn1 gena in klinično diagnozo sma tipa 1, orpatients z 5q sma z dvo-allelic mutacije v smn1 gena in do 3 kopije gena smn2.

Evropska unija - slovenščina - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - belantamab mafodotin - multiple myeloma - antineoplastična sredstva - 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.