Ninlaro Európai Unió - magyar - EMA (European Medicines Agency)

ninlaro

takeda pharma a/s - ixazomib citrátot - myeloma multiplex - daganatellenes szerek - a lenlidomiddal és a dexametazonnal kombinációban szenvedő ninlaro jelzett többszörös mielóma felnőtt betegek kezelésére, akik legalább egy korábbi terápiát kaptak.

Pepaxti Európai Unió - magyar - 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.

Imnovid (previously Pomalidomide Celgene) Európai Unió - magyar - EMA (European Medicines Agency)

imnovid (previously pomalidomide celgene)

bristol-myers squibb pharma eeig - pomalidomide - myeloma multiplex - immunszuppresszánsok - imnovid kombinálva bortezomib, valamint dexametazon jelzi a felnőtt betegek kezelésére myeloma multiplex, aki kapott már legalább egy előzetes kezelést-beleértve a lenalidomid. imnovid együtt dexametazon javallt kezelésére felnőtt kiújult és tűzálló myeloma multiplexes betegeknél, akik kaptak legalább két előzetes kezelési protokollok, beleértve a lenalidomid és bortezomib, és bebizonyították betegség progresszióját az utolsó terápia.

Nexpovio Európai Unió - magyar - EMA (European Medicines Agency)

nexpovio

stemline therapeutics b.v. - selinexor - myeloma multiplex - daganatellenes szerek - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

Abecma Európai Unió - magyar - EMA (European Medicines Agency)

abecma

bristol-myers squibb pharma eeig - idecabtagene vicleucel - multiple myeloma; neoplasms; cancer; neoplasms, plasma cell; hemostatic disorders; vascular diseases; cardiovascular diseases; paraproteinemias; blood protein disorders; hematologic diseases; hemic and lymphatic diseases; hemorrhagic disorders; infectious mononucleosis; lymphoproliferative disorders; immunoproliferative disorders; immune system diseases - daganatellenes szerek - abecma 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.