9780367483845-036748384X-Gene and Cell Therapies: Market Access and Funding (Pharmaceuticals, Health Economics and Market Access)

Gene and Cell Therapies: Market Access and Funding (Pharmaceuticals, Health Economics and Market Access)

ISBN-13: 9780367483845
ISBN-10: 036748384X
Edition: 1
Author: Eve Hanna, Mondher Toumi
Publication date: 2020
Publisher: CRC Press
Format: Hardcover 146 pages
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Book details

ISBN-13: 9780367483845
ISBN-10: 036748384X
Edition: 1
Author: Eve Hanna, Mondher Toumi
Publication date: 2020
Publisher: CRC Press
Format: Hardcover 146 pages

Summary

Gene and Cell Therapies: Market Access and Funding (Pharmaceuticals, Health Economics and Market Access) (ISBN-13: 9780367483845 and ISBN-10: 036748384X), written by authors Eve Hanna, Mondher Toumi, was published by CRC Press in 2020. With an overall rating of 3.8 stars, it's a notable title among other Pharmaceutical & Biotechnology (Industries, General & Reference, Chemistry, Medical Technology, Allied Health Professions, Chemistry, Pharmacology, Pharmacy) books. You can easily purchase or rent Gene and Cell Therapies: Market Access and Funding (Pharmaceuticals, Health Economics and Market Access) (Hardcover) from BooksRun, along with many other new and used Pharmaceutical & Biotechnology books and textbooks. And, if you're looking to sell your copy, our current buyback offer is $0.3.

Description

The major advances in the field of biotechnology and molecular biology in the twenty-first century have led to a better understanding of the pathophysiology of diseases. A new generation of biopharmaceuticals has emerged, including a wide and heterogeneous range of innovative cell and gene therapies. These therapies aim to prevent or treat chronic and serious life-threatening diseases, previously considered incurable. This book describes the evolution and adaptation of the regulatory environment to assess these therapies in contrast with the resistance of health technology assessment (HTA) agencies and payers to acknowledge the specificity of cell and gene therapies and the need to adapt existing decision-making frameworks. This book provides insights on the learnings from the experience of current cell and gene therapies (regulatory approval, HTA, and market access), in addition to future trends to enhance patient access to these therapies.

Key Features:

  • Describes the potential change of treatment paradigm and the specificity of cell and gene therapies, including the gradual move from repeated treatment administration to one-time single administration with the potential to be definite cure
  • Highlights the challenges at the HTA level
  • Discusses the affordability of future cell and gene therapies and the possible challenges for health insurance systems
  • Provides potential solutions to address these challenges and ensure patient access to innovation while maintaining the sustainability of healthcare systems

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