Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Filgrastim-sndz"'
Autor:
Daniel J. Weisdorf, Molly M. Jeffery, Jessica Chang, Pinar Karaca-Mandic, Stephen W. Schondelmeyer, Ronald S. Go
Publikováno v:
Health affairs (Project Hope). 38(11)
In 2015 the Food and Drug Administration approved filgrastim-sndz (Zarxio), the first US biosimilar. Following rapid uptake, by March 2018 filgrastim-sndz accounted for 47 percent of filgrastim administrations among commercially insured and 42 percen
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Publikováno v:
Journal of Clinical Oncology. 38:73-73
73 Background: According to clinical practice guidelines, the threshold for routine myeloid growth factor (MGF) PP is a high risk (>20%) of developing FN. However, in response to the COVID-19 pandemic, a recent recommendation expands this threshold f
Publikováno v:
Journal of Clinical Oncology. 38:e19401-e19401
e19401 Background: Patients with nonmetastatic NSCLC receiving platinum-based chemotherapy are at an intermediate risk (10-20%) of developing FN; clinical practice guidelines recommend assessing whether these patients have FN risk factors before cons
Publikováno v:
Journal of medical economics. 21(6)
McBride et al.1 recently published what was referred to as “cost-efficiency analyses”. The analyses completed by the authors compared four alternative granulocyte colony-stimulating factor (G-CSF) ...
Publikováno v:
Expert Opinion on Biological Therapy. 16:137-142
On March 6(th) 2015, the Food and Drug Administration (FDA) approved filgrastim-sndz (Zarxio) as the first biosimilar in the United States (US) for all indications of the reference product. Filgrastim-sndz is a biosimilar of Amgen's Neupogen and is m
Publikováno v:
Journal of medical economics. 20(10)
Aims: Guidelines recommend prophylaxis with granulocyte colony-stimulating factor for chemotherapy-induced (febrile) neutropenia (CIN/FN) based on regimen myelotoxicity and patient-related risk factors. The aim was to conduct a cost-efficiency analys
Engraftment with Filgrastim-Sndz Versus Filgrastim in Adult Autologous Stem Cell Transplant Patients
Publikováno v:
Biology of Blood and Marrow Transplantation. 24:S333-S334
Autor:
Jane De Lartigue
Publikováno v:
The Journal of Community and Supportive Oncology. 13:420-422
Publikováno v:
Journal of Clinical Oncology. 36:140-140
140 Background: G-CSFs are utilized to lower the incidence of febrile neutropenia (FN) in patients with cancers treated with chemotherapy. In 2015 filgrastim-sndz was the first biosimilar to be approved and launched in the US. Limited data exists on