Reversing Sickle Cell Disease: A Crisp Deal?
- ケース
- 新着ケース
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。