Европейски съюз - български - EMA (European Medicines Agency)

merck europe b.v. - tepotinib hydrochloride monohydrate - Карцином, недребноклетъчен белодроб - Антинеопластични средства - 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.

Европейски съюз - български - EMA (European Medicines Agency)

astellas pharma europe b.v. - gilteritinib фумарат - Левкемия, миелоиден, остър - Антинеопластични средства - xospata включен като монотерапии за лечение на възрастни пациенти с рецидив или продължителна остра миелоидна левкемия (ОМЛ) с перегласовкой flt3 по .

Европейски съюз - български - EMA (European Medicines Agency)

takeda pharma a/s - иксазомиб цитрат - Множествена миелома - Антинеопластични средства - ninlaro в комбинация с Леналидомид и дексаметазон е показан за лечение на възрастни пациенти с мултиплен миелом, които са получили поне една предварителна терапия.

Европейски съюз - български - EMA (European Medicines Agency)

astellas pharma europe b.v. - roxadustat - anemia; kidney failure, chronic - Антианемични препарати - evrenzo is indicated for treatment of adult patients with symptomatic anaemia associated with chronic kidney disease (ckd).

Европейски съюз - български - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - амбрисентан - Хипертония, белодробна - Гипотензивные, - volibris is indicated for treatment of pulmonary arterial hypertension (pah) in adult patients of who functional class (fc) ii to iii, including use in combination treatment (see section 5.  efficacy has been shown in idiopathic pah (ipah) and in pah associated with connective tissue disease. volibris is indicated for treatment of pah in adolescents and children (aged 8 to less than 18 years) of who functional class (fc) ii to iii including use in combination treatment. efficacy has been shown in ipah, familial, corrected congenital and in pah associated with connective tissue disease (see section 5.

Европейски съюз - български - EMA (European Medicines Agency)

novartis europharm limited  - capmatinib dihydrochloride monohydrate - Карцином, недребноклетъчен белодроб - Антинеопластични средства - tabrecta 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.

Европейски съюз - български - EMA (European Medicines Agency)

novo nordisk a/s - somapacitan - Растеж - Хипофизни и хипоталамични хормони и аналози - sogroya is indicated for the replacement of endogenous growth hormone (gh) in children  aged 3  years and above, and adolescents with growth failure due to growth hormone deficiency (paediatric ghd), and in adults with growth hormone deficiency (adult ghd).

Европейски съюз - български - EMA (European Medicines Agency)

alnylam netherlands b.v. - patisiran натрий - Амилоидоза, Фамилна - Други лекарства в нервната система - onpattro е показан за лечение на наследствени транстиретина-посредничанного амилоидоза (hattr амилоидоза) при възрастни пациенти с 1 етап 2 етап полиневропатия.

Европейски съюз - български - EMA (European Medicines Agency)

deciphera pharmaceuticals (netherlands) b.v. - ripretinib - Стомашно-чревни стромални тумори - Антинеопластични средства - qinlock is indicated for the treatment of adult patients with advanced gastrointestinal stromal tumour (gist) who have received prior treatment with three or more kinase inhibitors, including imatinib.

Европейски съюз - български - EMA (European Medicines Agency)

astrazeneca ab - selumetinib sulfate - neurofibromatosis 1 - Антинеопластични средства - koselugo as monotherapy is indicated for the treatment of symptomatic, inoperable plexiform neurofibromas (pn) in paediatric patients with neurofibromatosis type 1 (nf1) aged 3 years and above.