Zalmoxis Den Europæiske Union - dansk - EMA (European Medicines Agency)

zalmoxis

molmed spa - allogen t celler genetisk modificeret med en retroviral vektor kodning for en afkortet form af menneskelige lav affinitet nerve vækstfaktor receptor (Δlngfr) og herpes simplex virus thymidine kinase (hsv-tk mut2) - hematopoietic stem cell transplantation; graft vs host disease - antineoplastiske midler - zalmoxis er indiceret som supplerende behandling ved haploidentisk hæmatopoietisk stamcelle-transplantation (hsct) hos voksne patienter med højrisiko hæmatologiske maligniteter.

Horse Allo 20 Den Europæiske Union - dansk - EMA (European Medicines Agency)

horse allo 20

centauri biotech sl - allogen enhovede fedtvæv udvundet af mesenchymal stem cells - heste - til behandling af slidgigt hos voksne ikke-fødevareproducerende heste.

Phelinun Den Europæiske Union - dansk - 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 - antineoplastiske midler - 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.

Thiotepa Riemser Den Europæiske Union - dansk - EMA (European Medicines Agency)

thiotepa riemser

esteve pharmaceuticals gmbh - thiotepa - hematopoietic stem cell transplantation; neoplasms - antineoplastiske midler - thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients. thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients.

Blincyto Den Europæiske Union - dansk - EMA (European Medicines Agency)

blincyto

amgen europe b.v. - blinatumomab - forløbercellelimfoblastisk leukæmi-lymfom - antineoplastiske midler - blincyto is indicated as monotherapy for the treatment of adults with cd19 positive relapsed or refractory b precursor acute lymphoblastic leukaemia (all). patients with philadelphia chromosome positive b-precursor all should have failed treatment with at least 2 tyrosine kinase inhibitors (tkis) and have no alternative treatment options. blincyto is indicated as monotherapy for the treatment of adults with philadelphia chromosome negative cd19 positive b-precursor all in first or second complete remission with minimal residual disease (mrd) greater than or equal to 0. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with philadelphia chromosome negative cd19 positive b precursor all which is refractory or in relapse after receiving at least two prior therapies or in relapse after receiving prior allogeneic haematopoietic stem cell transplantation. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with high-risk first relapsed philadelphia chromosome negative cd19 positive b-precursor all as part of the consolidation therapy (see section 4.

Busilvex Den Europæiske Union - dansk - EMA (European Medicines Agency)

busilvex

pierre fabre medicament - busulfan - hematopoietisk stamcelletransplantation - antineoplastiske midler - busilvex efterfulgt af cyclophosphamid (bucy2) er indiceret som konditionerende behandling før konventionelle hæmatopoietiske stamceller celle transplantation (hpct) hos voksne patienter, når kombinationen er betragtes som den bedste tilgængelige mulighed. busilvex følgende fludarabine (fb) er angivet som condition behandling forud for hæmatopoietisk stamcelletransplantation (hpct) hos voksne patienter, der er kandidater til en reduceret intensitet conditioning (ric) opskrift. busilvex efterfulgt af cyclophosphamid (bucy4) eller melphalan (bumel) er angivet som condition behandling forud for konventionelle hæmatopoietisk stamcelletransplantation i pædiatriske patienter.

Busulfan Fresenius Kabi Den Europæiske Union - dansk - EMA (European Medicines Agency)

busulfan fresenius kabi

fresenius kabi deutschland gmbh - busulfan - hematopoietisk stamcelletransplantation - alkylsulfonater - busulfan fresenius kabi efterfulgt af cyclophosphamid (bucy2) er indiceret som konditionerende behandling før konventionelle hæmatopoietiske stamceller celle transplantation (hpct) hos voksne patienter, når kombinationen er betragtes som den bedste tilgængelige mulighed. busulfan fresenius kabi efterfulgt af cyclophosphamid (bucy4) eller melphalan (bumel) er angivet som condition behandling forud for konventionelle hæmatopoietisk stamcelletransplantation i pædiatriske patienter.

Arti-Cell Forte Den Europæiske Union - dansk - EMA (European Medicines Agency)

arti-cell forte

boehringer ingelheim vetmedica gmbh - chondrogenic induceret enhovede allogen perifert blod-afledte mesenchymal stem cells - andre midler mod forstyrrelser i muskel-skeletsystemet - heste - reduktion af mild til moderat periodisk halthed, der er forbundet med ikke-septisk ledbetændelse i heste.

Trecondi Den Europæiske Union - dansk - EMA (European Medicines Agency)

trecondi

medac gesellschaft für klinische spezialpräparate mbh - treosulfan - hematopoietisk stamcelletransplantation - antineoplastiske midler - treosulfan in combination with fludarabine is indicated as part of conditioning treatment prior to allogeneic haematopoietic stem cell transplantation (allohsct) in adult patients and in paediatric patients older than one month with malignant and non-malignant diseases.