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2021 Year in Review - Biosimilars
2021 Year in Review - Biosimilars
Scaled Integration of FDA-Approved Biosimilars
Biosimilars
2021 Year in Review - Biosimilars
A biosimilar adoption integration process that included full staff education, physician consent, and systematic auto- conversion proved to be feasible and scalable, and resulted in rapid conversion from reference product to FDA-approved biosimilar.
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Biosimilar Uptake of Filgrastim and Impact on Spending in Medicare Part D from 2015 to 2019
Biosimilars
2021 Year in Review - Biosimilars
A retrospective, cross-sectional review reported significant uptake of biosimilar filgrastim products in Medicare Part D from 2015 to 2019 being associated with a small decrease in aggregate spending, essentially unchanged per-unit spending, and increased spending per beneficiary on filgrastim products, all attributed to the inability of Medicare Part D to directly negotiate prices with manufacturers.
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Evaluation of Real-World Cost-Savings and Utilization of Biosimilar Drugs in a Community-Based Oncology Practice
Biosimilars
2021 Year in Review - Biosimilars
Prospective evaluation of real-world biosimilar-related cost-savings and adoption indicates that biosimilar utilization in community oncology practices can result in significant cost-savings.
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Utilization and Clinical Characteristics for the Trastuzumab Originator, Biosimilars, and Other HER2 Inhibitors
Biosimilars
2021 Year in Review - Biosimilars
The preliminary findings of a retrospective study that analyzed healthcare claims from the Biologics and Biosimilars Collective Intelligence Consortium’s Distributed Research Network between 2016 and 2020 indicate that utilization of biosimilar trastuzumab-anns increased over time, whereas the use of trastuzumab reference decreased.
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Cost-Savings from Conversion to Biosimilar Pegfilgrastim-cbqv Allowed Budget-Neutral Expanded Access to Antineoplastic Therapy
Biosimilars
2021 Year in Review - Biosimilars
Simulation models demonstrate substantial cost-savings realized by conversion to biosimilar pegfilgrastim-cbqv for chemotherapy-induced (febrile) neutropenia prophylaxis in patients with metastatic pancreatic cancer, and that these cost-savings could be reallocated to provide access to antineoplastic treatment on a budget-neutral basis.
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2021 in Review
Biosimilars
2021 Year in Review - Biosimilars
This past year, the COVID-19 pandemic continued to impact the practice of medicine and the dissemination of treatment advances presented in scientific forums.
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Bioequivalence of Bevacizumab Reference and Its Biosimilar BCD-021 in Nonsquamous NSCLC
Biosimilars
2021 Year in Review - Biosimilars
The results of a phase 3, randomized, double-blind study established the equivalence of bevacizumab reference to its biosimilar BCD-021 in terms of clinical efficacy, safety, pharmacokinetics, and immunogenicity in patients with NSCLC.
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Five-Year Follow-Up of a Comparative Phase 3 Study of SB3 and Trastuzumab Reference in HER2-Positive Early or Locally Advanced Breast Cancer
Biosimilars
2021 Year in Review - Biosimilars
The 5-year follow-up results of a comparative phase 3 study further support the similarity of SB3 and trastuzumab reference with respect to cardiac safety profile and long-term efficacy.
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Comparative Analysis of Safety, Efficacy, and Immunogenicity of Trastuzumab Reference and Its Biosimilar TX05 in HER2-Positive Early Breast Cancer
Biosimilars
2021 Year in Review - Biosimilars
The results of the randomized phase 3 TX05-03 study confirmed the therapeutic equivalence of trastuzumab reference and its biosimilar TX05 in terms of pathologic complete response, objective response rate, safety, and immunogenicity.
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Oncologists’ Knowledge and Perspectives on the Use of Biosimilars
Biosimilars
2021 Year in Review - Biosimilars
The findings of a survey of US oncologists indicate that practicing oncologists have gaps in their knowledge about biosimilars.
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Issues
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2024
February 2024 - Vol 17 No 1
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December 2023 - Vol 16 No 6
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ESMO 2023 - Small Cell Lung Cancer
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Best Practices in Breast Cancer Therapy | OFS
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CE
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