Concepts and challenges of biosimilars to mitigate the oncology drug expenses

dc.contributor.advisorHaque , Md. Aminul
dc.contributor.authorTania, Umme
dc.date.accessioned2021-10-03T09:01:45Z
dc.date.available2021-10-03T09:01:45Z
dc.date.issued2021-02
dc.descriptionCataloged from PDF version of thesis report.
dc.descriptionIncludes bibliographical references (pages 38-48).
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2021.
dc.description.abstractBiosimilars is way more likely to genuine generic drugs of the innovator. Time to time expiry of generic drugs helps manufacturer to think about biosimilars which has wide cost effectiveness as well as expanded patient accessibility to medicines especially for malignancy patients. This article gives a refreshed audit of the biosimilar pharmaceutical products affirmed for disease treatment in the US and EU through strict pre-clinical, clinical as well as pharmacovigilance touchstones. Diverse oncological biosimilar drugs that are right now being utilized like epoetins (alpha and zeta), filgrastim, as well as mAb (rituximab, trastuzumab and bevacizumab) are being exhibited in this article.
dc.identifier.otherID: 16346032
dc.identifier.otherhttps://dspace.bracu.ac.bd/server/api/core/items/4143ec84-9cb8-4e5e-9009-b6f147755e67
dc.identifier.urihttp://hdl.handle.net/10361/15111
dc.language.isoen_US
dc.publisherBRAC University
dc.sourceBRAC University Institutional Repository
dc.subjectBiosimilars
dc.subjectInterchangeability
dc.subjectCancer therapy
dc.subjectMonoclonal antibodies
dc.subjectBiologic medicines
dc.subjectComparability exercise
dc.titleConcepts and challenges of biosimilars to mitigate the oncology drug expenses
dc.typeThesis

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