Carvykti Unió Europea - hongarès - EMA (European Medicines Agency)

carvykti

janssen-cilag international nv - ciltacabtagene autoleucel - myeloma multiplex - 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.

Syncroprost, 0,250 mg/ml oldatos injekció szarvasmarhák, lovak, sertések és kecskék számára A.U.V. Hongria - hongarès - NÉBIH (Nemzeti Élelmiszerlánc-biztonsági Hivatal)

syncroprost, 0,250 mg/ml oldatos injekció szarvasmarhák, lovak, sertések és kecskék számára a.u.v.

ceva-phylaxia oltóanyagtermelo zrt. - kloprosztenol-nátrium - oldatos injekció - cloprostenol - szarvasmarha, kecske, sertés, ló

Pepaxti Unió Europea - hongarès - EMA (European Medicines Agency)

pepaxti

oncopeptides ab - melphalan flufenamide hydrochloride - myeloma multiplex - daganatellenes szerek - pepaxti is indicated, in combination with dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least three prior lines of therapies, whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and one anti-cd38 monoclonal antibody, and who have demonstrated disease progression on or after the last therapy. for patients with a prior autologous stem cell transplantation, the time to progression should be at least 3 years from transplantation (see section 4.

Tecvayli Unió Europea - hongarès - EMA (European Medicines Agency)

tecvayli

janssen-cilag international n.v. - teclistamab - myeloma multiplex - daganatellenes szerek - 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.

Columvi Unió Europea - hongarès - EMA (European Medicines Agency)

columvi

roche registration gmbh  - glofitamab - lymphoma, large b-cell, diffuse - daganatellenes szerek - columvi as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl), after two or more lines of systemic therapy.

Talvey Unió Europea - hongarès - EMA (European Medicines Agency)

talvey

janssen-cilag international n.v. - talquetamab - myeloma multiplex - daganatellenes szerek - 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.

Tepkinly Unió Europea - hongarès - EMA (European Medicines Agency)

tepkinly

abbvie deutschland gmbh & co. kg - epcoritamab - lymphoma, large b-cell, diffuse - daganatellenes szerek - tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b-cell lymphoma (dlbcl) after two or more lines of systemic therapy.