Besponsa Evropská unie - bulharština - EMA (European Medicines Agency)

besponsa

pfizer europe ma eeig - inotuzumab ozogamicin - Прекурсорна клетъчна лимфобластна левкемия-лимфом - Антинеопластични средства - besponsa включен като монотерапии за лечение на възрастни пациенти с пристъпно или продължителна cd22-положителни клетки b предшественици остра лимфоцитна левкемия (всички). При възрастни пациенти с положителна Филадельфийской хромозомата в яйцеклетката (рН+) повтарящите се или продължителна клетки предшественици следва този на изкуството на боравене с минимум 1 инхибитор на тирозинкиназы (cti).

Verzenios Evropská unie - bulharština - EMA (European Medicines Agency)

verzenios

eli lilly nederland b.v. - abemaciclib - Неоплазми на гърдата - Антинеопластични средства - early breast cancerverzenios in combination with endocrine therapy is indicated for the adjuvant treatment of adult patients with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative, node positive early breast cancer at high risk of recurrence (see section 5. in pre or perimenopausal women, aromatase inhibitor endocrine therapy should be combined with a luteinising hormone-releasing hormone (lhrh) agonist. advanced or metastatic breast cancerverzenios is indicated for the treatment of women with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative locally advanced or metastatic breast cancer in combination with an aromatase inhibitor or fulvestrant as initial endocrine-based therapy, or in women who have received prior endocrine therapy. in pre- or perimenopausal women, the endocrine therapy should be combined with a lhrh agonist.

Lorviqua Evropská unie - bulharština - EMA (European Medicines Agency)

lorviqua

pfizer europe ma eeig - lorlatinib - Карцином, недребноклетъчен белодроб - antineoplastic agents, protein kinase inhibitors - lorviqua as monotherapy is indicated for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. lorviqua as monotherapy is indicated for the treatment of adult patients with alk‑positive advanced nsclc whose disease has progressed after:alectinib or ceritinib as the first alk tyrosine kinase inhibitor (tki) therapy; orcrizotinib and at least one other alk tki.

Calquence Evropská unie - bulharština - EMA (European Medicines Agency)

calquence

astrazeneca ab - acalabrutinib - Левкемия, лимфоцитна, хронична, В-клетка - antineoplastic agents, protein kinase inhibitors, - calquence as monotherapy or in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll). calquence as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (cll) who have received at least one prior therapy.

Lumoxiti Evropská unie - bulharština - EMA (European Medicines Agency)

lumoxiti

astrazeneca ab - moxetumomab pasudotox - Левкемия, космат килия - Антинеопластични средства - lumoxiti as monotherapy is indicated for the treatment of adult patients with relapsed or refractory hairy cell leukaemia (hcl) after receiving at least two prior systemic therapies, including treatment with a purine nucleoside analogue (pna).

Koselugo Evropská unie - bulharština - EMA (European Medicines Agency)

koselugo

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.

Lumykras Evropská unie - bulharština - EMA (European Medicines Agency)

lumykras

amgen europe bv - sotorasib - Карцином, недребноклетъчен белодроб - Антинеопластични средства - lumykras as monotherapy is indicated for the treatment of adults with advanced non-small cell lung cancer (nsclc) with kras g12c mutation and who have progressed after at least one prior line of systemic therapy.

Saphnelo Evropská unie - bulharština - EMA (European Medicines Agency)

saphnelo

astrazeneca ab - anifrolumab - Лупус еритематозус, системен - Имуносупресори - saphnelo is indicated as an add-on therapy for the treatment of adult patients with moderate to severe, active autoantibody-positive systemic lupus erythematosus (sle), despite standard therapy.

Padcev Evropská unie - bulharština - EMA (European Medicines Agency)

padcev

astellas pharma europe b.v. - enfortumab vedotin - carcinoma, transitional cell; urologic neoplasms - Антинеопластични средства - 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.

Opdualag Evropská unie - bulharština - EMA (European Medicines Agency)

opdualag

bristol-myers squibb pharma eeig - nivolumab, relatlimab - Меланомът - antineoplastic agents, monoclonal antibodies - opdualag is indicated for the first line treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older with tumour cell pd l1 expression < 1%.