Acceptability of CYLTEZO pen among biologics autoinjector patients, autoinjector Naïve patients, and healthcare professionals

Author:

Perez Raul1,Suman Julie D2,Reynolds Joe1

Affiliation:

1. Noble International LLC, Orlando, Florida, USA

2. AptarGroup Inc, Congers, New York, USA

Funder

Boehringer Ingelheim Pharmaceuticals, Inc

Publisher

Informa UK Limited

Reference48 articles.

1. Similar efficacy, safety and immunogenicity of adalimumab biosimilar BI 695501 and Humira reference product in patients with moderately to severely active rheumatoid arthritis: results from the phase III randomised VOLTAIRE-RA equivalence study

2. Adalimumab-Adbm: The First Interchangeable Biosimilar for the Treatment of Inflammatory Diseases

3. Center for Biologics Evaluation and Research. Considerations in Demonstrating Interchangeability With a Reference Product Guidance for Industry. Silver Spring (MD): Food & Drug Administration (US); [updated 2020 May 6; cited 2023 Aug 31]. Available from: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/considerations-demonstrating-interchangeability-reference-product-guidance-industry

4. Center for Drug Evaluation and Research. Supplement Approval: Fulfillment of Postmarketing Requirement. Silver Spring (MD): US Food and Drug Administration; [cited 2023 Sep 18]. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/761058Orig1s008ltr.pdf

5. S.1695 - 110th Congress (2007-2008): Biologics Price Competition and Innovation Act of 2007. 2008 Nov 19.) Available from: https://www.congress.gov/bill/110th-congress/senate-bill/1695

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