Reversing Sickle Cell Disease: A Crisp Deal?

Matherne, G. (Paul) Herpfer, Christoph Dow, Ethan

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DARDEN

Carmen Jones, principal at a venture capital firm in the biotechnology industry, pondered the latest deal the firm was considering. It had recently closed a $700 million fund and was evaluating several early-stage drug development companies, among them Switch Infinity Therapeutics, which proved increasingly interesting the more she learned about it. Switch was utilizing cutting-edge CRISPR gene-editing technology for a gene therapy to permanently cure sickle cell disease, a major cause of death and disability. While this treatment had the potential to be both incredibly impactful and lucrative, it was a new therapy built on new technologies that carried a lot of risk, and investment in it would take a large portion of the capital in the new fund.

This public-sourced case introduces some key factors in decision-making around investing in new medical treatments. At the University of Virginia Darden School of Business, it is taught in the second-year “Healthcare Finance” course; due to its low technical requirements, it would also be suitable in an advanced undergraduate context or as a module on broader venture financing.

出版日
2025/11
業種
医療・医薬品
領域
生産・業務管理
財務
ボリューム
11ページ
コンテンツID
CCJB-UVA-OM-1795
オリジナルID
OM-1795
ケースの種類
Case
言語
英語
カラー
製本の場合、モノクロ印刷での納品となります。