Biosimilar agents in oncology/haematology: from approval to practice
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The emergence of biosimilar insulin preparations--a cause for concern?Expert perspectives on biosimilar monoclonal antibodies in breast cancerReview article: biosimilars are the next generation of drugs for liver and gastrointestinal diseasesRegulatory considerations in oncologic biosimilar drug developmentClinical considerations for biosimilar antibodies.Biosimilars: Implications for health-system pharmacists.A randomized, non-inferiority study comparing efficacy and safety of a single dose of pegfilgrastim versus daily filgrastim in pediatric patients after autologous peripheral blood stem cell transplantRecombinant glucagon: a differential biological activity.Regulatory and clinical considerations for biosimilar oncology drugsHerpes murine model as a biological assay to test dialyzable leukocyte extracts activity.Switching Between Epoetins: A Practice in Support of Biosimilar Use.Safety and efficacy of granulocyte colony-stimulating factor biosimilars in engraftment after autologous stem cell transplantation for haematological malignancies: a 4-year, single institute experience with different conditioning regimensDoctors commitment and long-term effectiveness for cost containment policies: lesson learned from biosimilar drugs.Assessing gastroenterologist and patient acceptance of biosimilars in ulcerative colitis and Crohn's disease across GermanyMobilization of PBSC for allogeneic transplantation by the use of the G-CSF biosimilar XM02 in healthy donors.Comparison of originator and biosimilar therapeutic monoclonal antibodies using comprehensive two-dimensional liquid chromatography coupled with time-of-flight mass spectrometry.Erythropoietin biosimilars currently available in hematology-oncology.Optimized granulocyte colony-stimulating factor prophylaxis in adult cancer patients: from biological principles to clinical guidelines.Biosimilar recombinant human erythropoietins ("epoetins") and future erythropoiesis-stimulating treatments.The safety of switching between therapeutic proteins.Epoetin biosimilars in Europe: five years on.Pharmacovigilance and biosimilars: considerations, needs and challenges.Clinical experience with Zarzio® in Europe: what have we learned?Biosimilar G-CSF based mobilization of peripheral blood hematopoietic stem cells for autologous and allogeneic stem cell transplantationLong-active granulocyte colony-stimulating factor for peripheral blood hematopoietic progenitor cell mobilization.Biosimilars: Hope and concern.Current Status of Biosimilars in Oncology.Is there a reason for concern or is it just hype? - A systematic literature review of the clinical consequences of switching from originator biologics to biosimilars.Tbo-Filgrastim: A Review in Neutropenic Conditions.Interchangeability among reference insulin analogues and their biosimilars: regulatory framework, study design and clinical implications.Assessing physician and patient acceptance of infliximab biosimilars in rheumatoid arthritis, ankylosing spondyloarthritis and psoriatic arthritis across Germany.Evaluation of a biosimilar granulocyte colony-stimulating factor (filgrastim XM02) for peripheral blood stem cell mobilization and transplantation: a single center experience in Japan.Cost savings from anemia management with biosimilar epoetin alfa and increased access to targeted antineoplastic treatment: a simulation for the EU G5 countries.Key concepts and critical issues on epoetin and filgrastim biosimilars. A position paper from the Italian Society of Hematology, Italian Society of Experimental Hematology, and Italian Group for Bone Marrow Transplantation.Anti-neoplastic biosimilars--the same rules as for cytotoxic generics cannot be applied.Biosimilar rhG-CSFs: how similar are they?Improving Access to Cancer Treatments: The Role of Biosimilars.The Concept of Biosimilars: From Characterization to Evolution-A Narrative Review.A comparative analysis of biosimilar vs. originator filgrastim in combination with plerixafor for stem cell mobilization in lymphoma and multiple myeloma: a propensity-score weighted multicenter approach.A randomized, multi-center, open-label, phase II study of once-per-cycle DA-3031, a biosimilar pegylated G-CSF, compared with daily filgrastim in patients receiving TAC chemotherapy for early-stage breast cancer.
P2860
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P2860
Biosimilar agents in oncology/haematology: from approval to practice
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Biosimilar agents in oncology/haematology: from approval to practice
@ast
Biosimilar agents in oncology/haematology: from approval to practice
@en
Biosimilar agents in oncology/haematology: from approval to practice
@nl
type
label
Biosimilar agents in oncology/haematology: from approval to practice
@ast
Biosimilar agents in oncology/haematology: from approval to practice
@en
Biosimilar agents in oncology/haematology: from approval to practice
@nl
prefLabel
Biosimilar agents in oncology/haematology: from approval to practice
@ast
Biosimilar agents in oncology/haematology: from approval to practice
@en
Biosimilar agents in oncology/haematology: from approval to practice
@nl
P2860
P1476
Biosimilar agents in oncology/haematology: from approval to practice
@en
P2093
Dietger Niederwieser
Stephan Schmitz
P2860
P304
P356
10.1111/J.1600-0609.2010.01566.X
P577
2011-01-25T00:00:00Z
2011-04-01T00:00:00Z