How Much Are Biosimilars Used in Clinical Practice? A Retrospective Italian Population-Based Study of Erythropoiesis-Stimulating Agents in the Years 2009–2013

Author:

Ingrasciotta Ylenia,Giorgianni Francesco,Bolcato Jenny,Chinellato Alessandro,Pirolo Roberta,Tari Daniele Ugo,Troncone Chiara,Fontana Andrea,Ientile Valentina,Gini Rosa,Santoro Domenico,Santarpia Mariacarmela,Genazzani Armando,Uomo Ilaria,Pastorello Maurizio,Addario Walter Sebastiano Pollina,Scondotto Salvatore,Cananzi Pasquale,Caputi Achille Patrizio,Trifirò Gianluca

Funder

Italian Health Minister

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology,General Medicine,Biotechnology

Reference33 articles.

1. Blackstone EA, Fuhr JP. The economics of biosimilars. Am Health Drug Benefits. 2013;6(8):469–78.

2. Ventola CL. Biosimilars: part 1. Proposed regulatory criteria for FDA approval. Pharm Ther. 2013;38(5):270–87.

3. European Medicines Agency. Committee for Medicinal Products for Human Use (CHMP): guideline on similar biological medicinal products containing biotechnology-derived proteins as active substance: non-clinical and clinical issues. Available from: http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2013/06/WC500144124.pdf .

4. Agenzia Italiana del Farmaco (AIFA). Position paper sui farmaci biosimilari (28/05/2013). Available from: http://www.agenziafarmaco.gov.it/sites/default/files/AIFA_POSITION_PAPER_FARMACI_BIOSIMILARI.pdf .

5. Genazzani AA, Biggio G, Caputi AP, et al. Biosimilar drugs: concerns and opportunities. Biodrugs. 2007;21:351–6.

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