Literature DB >> 24589534

Stakeholders discuss biosimilar naming, substitution.

Kate Traynor.   

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Year:  2014        PMID: 24589534     DOI: 10.2146/news140023

Source DB:  PubMed          Journal:  Am J Health Syst Pharm        ISSN: 1079-2082            Impact factor:   2.637


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  4 in total

Review 1.  Regulatory and clinical considerations for biosimilar oncology drugs.

Authors:  Charles L Bennett; Brian Chen; Terhi Hermanson; Michael D Wyatt; Richard M Schulz; Peter Georgantopoulos; Samuel Kessler; Dennis W Raisch; Zaina P Qureshi; Z Kevin Lu; Bryan L Love; Virginia Noxon; Laura Bobolts; Melissa Armitage; John Bian; Paul Ray; Richard J Ablin; William J Hrushesky; Iain C Macdougall; Oliver Sartor; James O Armitage
Journal:  Lancet Oncol       Date:  2014-11-24       Impact factor: 41.316

Review 2.  A Framework for Integrating Biosimilars Into the Didactic Core Requirements of a Doctor of Pharmacy Curriculum.

Authors:  Edward Li; Jennifer Liu; Monica Ramchandani
Journal:  Am J Pharm Educ       Date:  2017-04       Impact factor: 2.047

Review 3.  Regulatory considerations in oncologic biosimilar drug development.

Authors:  Judith C Macdonald; Helen Hartman; Ira A Jacobs
Journal:  MAbs       Date:  2015       Impact factor: 5.857

Review 4.  Clinical and regulatory perspectives on biosimilar therapies and intended copies of biologics in rheumatology.

Authors:  Eduardo Mysler; Carlos Pineda; Takahiko Horiuchi; Ena Singh; Ehab Mahgoub; Javier Coindreau; Ira Jacobs
Journal:  Rheumatol Int       Date:  2016-02-27       Impact factor: 2.631

  4 in total

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