Fingolimod Accord यूरोपीय संघ - जर्मन - EMA (European Medicines Agency)

fingolimod accord

accord healthcare s.l.u. - fingolimod hydrochloride - multiple sklerose, schubförmig-remittierender - immunsuppressiva, selektive immunsuppressiva - angegeben als einzige krankheitsmodifizierende therapie bei hochaktiver schubförmiger multipler sklerose bei folgenden gruppen erwachsener patienten und pädiatrischen patienten im alter von 10 jahren und älter:die patienten mit hoch aktiver erkrankung trotz einer vollständigen und adäquaten therapie mit mindestens einem krankheitsmodifizierenden therapyorpatients mit sich rasch entwickelnden schweren schubförmig remittierender multipler sklerose, definiert durch 2 oder mehr deaktivieren schübe in einem jahr, und mit 1 oder mehr gadolinium verbesserung läsionen auf gehirn-mrt oder eine signifikante zunahme der t2-läsionen laden als im vergleich zu einer früheren letzten mrt.

Sarclisa यूरोपीय संघ - जर्मन - EMA (European Medicines Agency)

sarclisa

sanofi winthrop industrie - isatuximab - multiples myelom - antineoplastische mittel - sarclisa is indicated: in combination with pomalidomide and dexamethasone, for the treatment of adult patients with relapsed and refractory multiple myeloma (mm) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor (pi) and have demonstrated disease progression on the last therapy. in combination with carfilzomib and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least one prior therapy (see section 5.

Blenrep यूरोपीय संघ - जर्मन - EMA (European Medicines Agency)

blenrep

glaxosmithkline (ireland) limited - belantamab mafodotin - multiples myelom - antineoplastische mittel - blenrep is indicated as monotherapy 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 one proteasome inhibitor, one immunomodulatory agent, and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

Fampridine Accord यूरोपीय संघ - जर्मन - EMA (European Medicines Agency)

fampridine accord

accord healthcare s.l.u. - fampridine - multiple sklerose - andere medikamente des nervensystems - fampridine accord is indicated for the improvement of walking in adult patients with multiple sclerosis with walking disability (edss 4-7).

Phelinun यूरोपीय संघ - जर्मन - EMA (European Medicines Agency)

phelinun

adienne s.r.l. s.u. - melphalan hydrochloride - multiple myeloma; hodgkin disease; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; leukemia, myeloid, acute; neuroblastoma; ovarian neoplasms; hematopoietic stem cell transplantation - antineoplastische mittel - high-dose of phelinun used alone or in combination with other cytotoxic medicinal products and/or total body irradiation is indicated in the treatment of:multiple myeloma,malignant lymphoma (hodgkin, non-hodgkin lymphoma),acute lymphoblastic and myeloblastic leukemia,childhood neuroblastoma,ovarian cancer,mammary adenocarcinoma. phelinun in combination with other cytotoxic medicinal products is indicated as reduced intensity conditioning (ric) treatment prior to allogeneic haematopoietic stem cell transplantation (allo-hsct) in malignant haematological diseases in adults. phelinun in combination with other cytotoxic medicinal products is indicated as conditioning regimen prior to allogeneic haematopoietic stem cell transplantation in haematological diseases in the paediatric population as:myeloablative conditioning (mac) treatment in case of malignant haematological diseasesric treatment in case of non-malignant haematological diseases.

Kesimpta यूरोपीय संघ - जर्मन - EMA (European Medicines Agency)

kesimpta

novartis ireland ltd - ofatumumab - multiple sklerose, schubförmig-remittierender - immunosuppressant - kesimpta is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features (see section 5.

Ponvory यूरोपीय संघ - जर्मन - EMA (European Medicines Agency)

ponvory

janssen-cilag international n.v.    - ponesimod - multiple sklerose, schubförmig-remittierender - immunsuppressiva - ponvory is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features.

Nexpovio यूरोपीय संघ - जर्मन - EMA (European Medicines Agency)

nexpovio

stemline therapeutics b.v. - selinexor - multiples myelom - antineoplastische mittel - 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.

Fingolimod Mylan यूरोपीय संघ - जर्मन - EMA (European Medicines Agency)

fingolimod mylan

mylan ireland limited - fingolimod hydrochloride - multiple sklerose, schubförmig-remittierender - immunsuppressiva - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older:patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 und 5. 1)orpatients mit sich rasch entwickelnden schweren schubförmig remittierender multipler sklerose, definiert durch 2 oder mehr deaktivieren schübe in einem jahr, und mit 1 oder mehr gadolinium verbesserung läsionen auf gehirn-mrt oder eine signifikante zunahme der t2-läsionen laden als im vergleich zu einer früheren letzten mrt.

Abecma यूरोपीय संघ - जर्मन - 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 - antineoplastische mittel - 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.