Opsumit Unjoni Ewropea - Malti - EMA (European Medicines Agency)

opsumit

janssen-cilag international n.v.   - macitentan - pressjoni għolja, pulmonari - għal pressjoni għolja, - opsumit, bħala monoterapija jew flimkien, huwa indikat għat-trattament fit-tul ta 'pressjoni għolja arterjali pulmonari (pah) f'pazjenti adulti tal-klassi funzjonali tal-who (fc) ii sa iii. l-effikaċja ġiet murija fil-pah popolazzjoni inkluż idjopatika u li tintiret mill-pah, li l-pah assoċjata mal-connective tissue, u pah assoċjata ma kkoreġuti sempliċi mard tal-qalb konġenitali.

Alecensa Unjoni Ewropea - Malti - EMA (European Medicines Agency)

alecensa

roche registration gmbh - alectinib hydrochloride - karċinoma, pulmun mhux taċ-Ċellula Żgħira - aġenti antineoplastiċi - alecensa bħala monoterapija hija indikata għat-trattament tal-ewwel linja ta 'pazjenti adulti b'kanċer tal-pulmun taċ-ċelluli mhux żgħar żgħar (nsclc) b'posfoma kinase anaplastika (alk). alecensa bħala monoterapija hija indikata għat-trattament ta ' pazjenti adulti bil-alk‑pożittivi nsclc avvanzat li qabel kienu kkurati bil-krizotinib.

Zinbryta Unjoni Ewropea - Malti - EMA (European Medicines Agency)

zinbryta

biogen idec ltd - daclizumab - sklerosi multipla - immunosoppressanti - zinbryta huwa indikat f'pazjenti adulti għat-trattament ta 'forom ta' sklerożi multipla li tirkadi (rms).

Kevzara Unjoni Ewropea - Malti - EMA (European Medicines Agency)

kevzara

sanofi winthrop industrie - sarilumab - artrite, rewmatika - immunosoppressanti - kevzara flimkien ma ' methotrexate (mtx) huwa indikat għall-kura tal-moderat biex severament attiva rewmatojde artrite (ra) fil-pazjenti adulti li jkollhom irrispondiet jirriżultax, jew li huma intolerant għall-marda waħda jew aktar li jimmodifika anti-rheumatic id-drogi (dmards). kevzara jista 'jingħata bħala monoterapija f'każ ta' intolleranza għal mtx jew meta t-trattament b'mtx mhuwiex xieraq.

Tremfya Unjoni Ewropea - Malti - EMA (European Medicines Agency)

tremfya

janssen-cilag international nv - guselkumab - psorajiżi - immunosoppressanti - plaque psoriasis tremfya is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritis tremfya, alone or in combination with methotrexate (mtx), is indicated for the treatment of active psoriatic arthritis in adult patients who have had an inadequate response or who have been intolerant to a prior disease-modifying antirheumatic drug (dmard) therapy (see section 5.

Steglatro Unjoni Ewropea - Malti - EMA (European Medicines Agency)

steglatro

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic acid - diabetes mellitus, tip 2 - drugs used in diabetes, sodium-glucose co-transporter 2 (sglt2) inhibitors - steglatro huwa indikat f'adulti ta '18-il sena u akbar b'dijabete mellitus tip 2 bħala żieda mad-dieta u l-eżerċizzju biex itejjeb il-kontroll gliċemiku:bħala monoterapija f'pazjenti li għalihom l-użu ta' metformin huwa kkunsidrat xieraq minħabba 'intolleranza jew ta' kontra-indikazzjonijiet. barra minn hekk oħra prodotti mediċinali għall-kura tad-dijabete.

Nubeqa Unjoni Ewropea - Malti - EMA (European Medicines Agency)

nubeqa

bayer ag - darolutamide - prostatika neoplażmi, il-kastrazzjoni-reżistenti - terapija endokrinali - nubeqa is indicated for the treatment of adult men with- non metastatic castration resistant prostate cancer (nmcrpc) who are at high risk of developing metastatic disease (see section 5. - metastatic hormone sensitive prostate cancer (mhspc) in combination with docetaxel and androgen deprivation therapy (see section 5.

Ayvakyt Unjoni Ewropea - Malti - EMA (European Medicines Agency)

ayvakyt

blueprint medicines (netherlands) b.v. - avapritinib - tumur stromali gastrointestinali - aġenti antineoplastiċi oħra, inibituri tal-proteina kinase - ayvakyt is indicated as monotherapy for the treatment of adult patients with unresectable or metastatic gastrointestinal stromal tumours (gist) harbouring the platelet-derived growth factor receptor alpha (pdgfra) d842v mutation.

Trodelvy Unjoni Ewropea - Malti - EMA (European Medicines Agency)

trodelvy

gilead sciences ireland uc - sacituzumab govitecan - breast neoplasms; triple negative breast neoplasms - aġenti antineoplastiċi - trodelvy as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic triple-negative breast cancer (mtnbc) who have received two or more prior systemic therapies, including at least one of them for advanced disease.

Padcev Unjoni Ewropea - Malti - EMA (European Medicines Agency)

padcev

astellas pharma europe b.v. - enfortumab vedotin - carcinoma, transitional cell; urologic neoplasms - aġenti antineoplastiċi - padcev as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial cancer who have previously received a platinum-containing chemotherapy and a programmed death receptor 1 or programmed death ligand 1 inhibitor.