Unjoni Ewropea - Malti - EMA (European Medicines Agency)

ipsen pharma - cabozantinib (s)-malate - carcinoma, renal cell; carcinomas, hepatocellular - aġenti antineoplastiċi - renal cell carcinoma (rcc)cabometyx is indicated as monotherapy for the treatment of advanced renal cell carcinoma (rcc):in treatment-naïve adults with intermediate or poor risk,in adults following prior vascular endothelial growth factor (vegf)-targeted therapy. cabometyx, in combination with nivolumab, is indicated for the first-line treatment of advanced renal cell carcinoma in adults. hepatocellular carcinoma (hcc)cabometyx is indicated as monotherapy for the treatment of hepatocellular carcinoma (hcc) in adults who have previously been treated with sorafenib.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

merck europe b.v. - tepotinib hydrochloride monohydrate - karċinoma, pulmun mhux taċ-Ċellula Żgħira - aġenti antineoplastiċi - tepmetko as monotherapy is indicated for the treatment of adult patients with advanced non-small cell lung cancer (nsclc) harbouring alterations leading to mesenchymal-epithelial transition factor gene exon 14 (metex14) skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum-based chemotherapy.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

laboratoire francais du fractionnement et des biotechnologies - eptacog beta (activated) - hemophilia a; hemophilia b - sustanzi kontra l-emorraġija - cevenfacta is indicated in adults and adolescents (12 years of age and older) for the treatment of bleeding episodes and for the prevention of bleeding in those undergoing surgery or invasive procedures in the following patient groups:in patients with congenital haemophilia with high-responding inhibitors to coagulation factors viii or ix (i. ≥5 bethesda units (bu)); in patients with congenital haemophilia with low titre inhibitors (bu.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

orion corporation - pregabalin - antiepileptics - qtates - alleviation of acute anxiety and fear associated with transportation and veterinary visits.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

astrazeneca ab - fulvestrant - neoplażmi tas-sider - endokrinali it-terapija, anti-estroġeni - faslodex is indicated , as monotherapy for the treatment of estrogen receptor positive, locally advanced or metastatic breast cancer in postmenopausal women:, , not previously treated with endocrine therapy, or, with disease relapse on or after adjuvant antiestrogen therapy, or disease progression on antiestrogen therapy. , , , in combination with palbociclib for the treatment of hormone receptor (hr)-positive, human epidermal growth factor receptor 2 (her2)-negative locally advanced or metastatic breast cancer in women who have received prior endocrine therapy. , fil - pre- jew perimenopausal-nisa, il-kombinazzjoni tat-trattament bil-palbociclib għandu jkun ikkombinat ma ' ormon luteinizing releasing hormone (lhrh) agonist.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

roche registration gmbh - bevacizumab - carcinoma, non-small-cell lung; breast neoplasms; ovarian neoplasms; colorectal neoplasms; carcinoma, renal cell - aġenti antineoplastiċi - bevacizumab flimkien ma 'kimoterapija bbażata fuq fluoropyrimidine huwa indikat għall-kura ta' pazjenti adulti b'karċinoma metastatika tal-kolon jew tar-rektum. bevacizumab f'kombinazzjoni ma 'paclitaxel, huwa indikat għall-kura preferita ta' pazjenti adulti b'kanċer metastatiku tas-sider. għal aktar informazzjoni kif tal-bniedem tar-riċettur tal-fattur tat-tkabbir epidermali 2 (her2) status. bevacizumab f'kombinazzjoni ma 'capecitabine huwa indikat għall-kura preferita ta' pazjenti adulti b'kanċer metastatiku tas-sider li fihom it-trattament bil-kimoterapija oħra għażliet inklużi l-tassani jew antraċiklini ma jkunx ikkunsidrat xieraq. pazjenti li rċivew korsijiet li fihom taxxaane u anthracycline fl-istabbiliment awżiljarju fl-aħħar 12-il xahar għandhom jiġu esklużi mit-trattament b'avastin flimkien ma 'capecitabine. għal aktar informazzjoni dwar her2-istatus. bevacizumab, barra minn hekk 'kimoterapija bbażata fuq platinum, huwa ndikat għall-kura preferita ta' pazjenti adulti li ma jistax jitneħħa, avvanzat, li mmetastatizza jew rikorrenti taċ-ċelluli mhux żgħar tal-pulmun il-kanċer l-oħra mill-aktar istoloġija ta ' ċelluli skwamużi. bevacizumab, f'kombinazzjoni ma 'erlotinib, huwa indikat għall-kura preferita ta' pazjenti adulti li ma jistax jitneħħa, avvanzat, li mmetastatizza jew rikorrenti mhux squamous taċ-ċelluli mhux żgħar tal-pulmun il-kanċer mar-riċettur tal-fattur tat-tkabbir epidermali (egfr) mutazzjonijiet li jattivaw. bevacizumab f'kombinazzjoni ma 'interferon alfa-2a huwa indikat għall-ewwel linja tal-kura ta' pazjenti adulti b'avvanzat u/jew metastatiku taċ-ċelluli renali kanċer. bevacizumab, f'kombinazzjoni ma 'carboplatin u paclitaxel huwa ndikat għall-quddiem il-linja ta 'trattament ta' pazjenti adulti b'avvanzati (il-federazzjoni internazzjonali tal-mard tal-ġilda u l-ostetriċja (medjevali) stadji iii b, iii u iv) ta 'l-epitilju ta' l-ovarji, l-tubu fallopjan, jew primarja peritoneali-kanċer. bevacizumab, f'kombinazzjoni ma 'carboplatin u gemcitabine, huwa indikat għall-kura ta' pazjenti adulti bil-ewwel rikorrenza tal-sensittiva għall-platinum ta 'l-epitilju ta' l-ovarji, l-tubu fallopjan jew primarja peritoneali-kanċer li ma rċevew terapija minn qabel ma 'bevacizumab, jew l-oħra' impedituri vegf jew vegf–riċetturi fil-mira l-aġenti. bevacizumab f'kombinazzjoni ma 'paclitaxel, topotecan, jew pegylated liposomal doxorubicin huwa indikat għat-trattament ta' pazjenti adulti bil-platinu-reżistenti rikorrenti ta 'l-epitilju ta' l-ovarji, l-tubu fallopjan, jew primarja peritoneali-kanċer li ma rċeviet l-ebda aktar minn żewġ qabel ma 'korsijiet ta' kimoterapija u li qatt ma kienu rċevew terapija minn qabel ma 'bevacizumab, jew l-oħra' impedituri vegf jew vegf–riċetturi fil-mira l-aġenti. bevacizumab, flimkien ma 'paclitaxel u cisplatin jew, alternattivament, paclitaxel u topotecan f'pazjenti li ma jistgħux jirċievu l-platinum-terapija, huwa indikat għall-kura ta' pazjenti adulti b'persistenti, rikorrenti, jew karċinoma metastatika taċ-ċerviċi.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - afatinib - karċinoma, pulmun mhux taċ-Ċellula Żgħira - aġenti antineoplastiċi - giotrif bħala monoterapija hija indikata għat-trattament ofepidermal growth factor receptor (egfr) tki pazjenti adulti naΐve għal kura bil-lokalment avvanzat jew dak metastatiku li mhux ta 'ċelluli żgħar kanċer tal-pulmun (nsclc) ma' l-attivazzjoni tal-egfr-mutazzjoni tal - (s);lokalment avvanzat jew metastatiku nsclc tal-kanser skwamuż tar-istoloġija tal-progress fuq jew wara ibbażat fuq il-platinu ' kimoterapija.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

zoetis belgium sa - synthetic peptide analogue of gnrf conjugated to diptheria toxoid - immunoloġiċi għal suidae - male pigs (from 8 weeks of age); female pigs (from 14 weeks of age) - male pigs:induction of antibodies against gnrf to produce a temporary immunological suppression of testicular function. for use as an alternative to physical castration for the reduction of boar taint caused by the key boar taint compound androstenone, in entire male pigs following the onset of puberty. kontributur ewlieni ieħor għall-tifqigħa tal-ħanżir, skatole, jista 'jitnaqqas ukoll bħala effett indirett. mġieba aggressiva u sesswali (immuntar) huma wkoll imnaqqsa. female pigs:induction of antibodies against gnrf to produce a temporary immunological suppression of ovarian function (suppression of oestrus) in order to reduce the incidence of unwanted pregnancies in gilts intended for slaughter, and to reduce the associated sexual behaviour (standing oestrus).

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

eli lilly nederland b.v. - olaratumab - sarcoma - aġenti antineoplastiċi - lartruvo hija indikata fil kombinazzjoni ma ' doxorubicin għat-trattament tal-pazjenti adulti b ' sarcoma artab avvanzati tat-tessuti li m'humiex soġġetti għal trattament kurattivi bil-kirurġija jew radjoterapija u li ma ġewx qabel trattati b ' doxorubicin (ara taqsima 5.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

molmed spa - Ċelloli alloġeniċi t ġenetikament modifikati ma vettoru retroviral kodifikar għall-formola maqtugħ ta ' l-affinità bniedem baxx ir-riċevitur fattur tat-tkabbir tal-ħsara (Δlngfr) u l-simplex herpes virus thymidine kinase (tk tat-hsv mut2) - hematopoietic stem cell transplantation; graft vs host disease - aġenti antineoplastiċi - zalmoxis huwa indikat bħala trattament adjunctive fl-trapjant ta ' ċelluli staminali ematopojetika haploidentical (hsct) ta ' l-pazjenti adulti ma malignancies ħematoloġiċi b'riskju għoli.