Europäische Union - Bulgarisch - EMA (European Medicines Agency)

janssen-cilag international nv - ciltacabtagene autoleucel - Множествена миелома - carvykti is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Europäische Union - Bulgarisch - EMA (European Medicines Agency)

theramex ireland limited - linzagolix choline - Лейомиома - Хипофизни и хипоталамични хормони и аналози - yselty is indicated for the treatment of moderate to severe symptoms of uterine fibroids in adult women of reproductive age.

Europäische Union - Bulgarisch - EMA (European Medicines Agency)

janssen-cilag international n.v. - teclistamab - Множествена миелома - Антинеопластични средства - tecvayli is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Europäische Union - Bulgarisch - EMA (European Medicines Agency)

janssen-cilag international n.v. - abiraterone acetate, niraparib tosilate monohydrate - Новообразувания На Простатата, Кастраци-Упорит - Антинеопластични средства - treatment of adult patients with prostate cancer.

Europäische Union - Bulgarisch - EMA (European Medicines Agency)

merck sharp & dohme b.v. - gefapixant - cough - Кашлица и студени препарати - lyfnua is indicated in adults for the treatment of refractory or unexplained chronic cough.

Europäische Union - Bulgarisch - EMA (European Medicines Agency)

janssen-cilag international n.v. - talquetamab - Множествена миелома - Антинеопластични средства - talvey is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least 3 prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti cd38 antibody and have demonstrated disease progression on the last therapy.