Literature DB >> 26105205

Biologics and biosimilars.

Palak K Patel1, Caleb R King, Steven R Feldman.   

Abstract

Biological drugs are large, complex glycoprotein molecules produced in living organisms. Revolutionary treatments for many conditions, biologics used in dermatology will face patent expiration, opening opportunities for competitive versions. Biologic drugs are so complex such that it is impossible to reproduce them exactly. Biosimilars are designed to be highly similar, though not identical, to the innovator product. Because biosimilars are not exact replicates of innovator biologics, guidelines have suggested that biosimilars should be considered as unique therapeutic interventions, requiring unique names and physician notification prior to substitution. However, because biologics can never be replicated exactly, even innovator biologics have inherent batch-to-batch variability; when the second batch of innovator products were released, physicians began prescribing non-identical variants of biologics to their patients, accepting the possibility of variation in clinical effects. Unlike the variants in innovator products, biosimilars will provide clinical trial data demonstrating similar clinical effects, though there will always be some degree of uncertainty in how much clinical impact will be result from the variation in both innovator and biosimilar products. How biosimilars are approved and how we use biosimilars will need to balance considerations of cost and development time with the possibility of variation in biological response.

Entities:  

Keywords:  Biologics; biosimilars; interchangeability; low-molecular weight drug; manufacturing; variability

Mesh:

Substances:

Year:  2015        PMID: 26105205     DOI: 10.3109/09546634.2015.1054782

Source DB:  PubMed          Journal:  J Dermatolog Treat        ISSN: 0954-6634            Impact factor:   3.359


  6 in total

1.  Comparing safety information of biosimilars with their originators: a cross-sectional analysis of European risk management plans.

Authors:  Leroy R A Lepelaars; Francesca Renda; Luca Pani; Giuseppe Pimpinella; Hubert G M Leufkens; Gianluca Trifirò; Giovanni Tafuri; Aukje K Mantel-Teeuwisse; Francesco Trotta
Journal:  Br J Clin Pharmacol       Date:  2018-01-18       Impact factor: 4.335

2.  Knowledge, Attitude, and Practice Towards Biosimilars and Interchangeable Products: A Prescriptive Insight by the Pharmacists.

Authors:  Sadia Shakeel; Mohamed Azmi Hassali; Hina Rehman; Anees Ur Rehman; Jaya Muneswarao
Journal:  Int J Gen Med       Date:  2020-11-11

3.  Utilizing graph machine learning within drug discovery and development.

Authors:  Thomas Gaudelet; Ben Day; Arian R Jamasb; Jyothish Soman; Cristian Regep; Gertrude Liu; Jeremy B R Hayter; Richard Vickers; Charles Roberts; Jian Tang; David Roblin; Tom L Blundell; Michael M Bronstein; Jake P Taylor-King
Journal:  Brief Bioinform       Date:  2021-11-05       Impact factor: 11.622

4.  Patient perspectives on the British Columbia Biosimilars Initiative: a qualitative descriptive study.

Authors:  Caitlin Chew; Magda Aguiar; Nick Bansback; Michael R Law; Mark Harrison
Journal:  Rheumatol Int       Date:  2021-05-07       Impact factor: 3.580

5.  Clozapine Induces an Acute Proinflammatory Response That Is Attenuated by Inhibition of Inflammasome Signaling: Implications for Idiosyncratic Drug-Induced Agranulocytosis.

Authors:  Samantha Christine Sernoskie; Alexandra R Lobach; Ryuji Kato; Alison Jee; Joseph Kyle Weston; Jack Uetrecht
Journal:  Toxicol Sci       Date:  2022-02-28       Impact factor: 4.849

Review 6.  mRNA Therapeutic Modalities Design, Formulation and Manufacturing under Pharma 4.0 Principles.

Authors:  Andreas Ouranidis; Theofanis Vavilis; Evdokia Mandala; Christina Davidopoulou; Eleni Stamoula; Catherine K Markopoulou; Anna Karagianni; Kyriakos Kachrimanis
Journal:  Biomedicines       Date:  2021-12-27
  6 in total

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