Bukini Daima, Makani Julie, McCune Joseph, Lee Dennis, Bansbach Cathy, De Vita Serena, Kemps Dominic, Amin Elianna, Spector Jonathan, Tisdale John
Sickle Cell Disease Program, Muhimbili University of Health and Allied Sciences, Dar es Salaam 65001, Tanzania.
SickleInAfrica, Clinical Coordinating Center, Muhimbili University of Health and Allied Sciences, Dar es Salaam 65001, Tanzania.
Mol Ther Methods Clin Dev. 2024 Jun 22;32(3):101287. doi: 10.1016/j.omtm.2024.101287. eCollection 2024 Sep 12.
Therapeutic innovation to address sickle cell disease (SCD) is at a historical apex, characterized by a drug discovery, development, and commercialization landscape that includes potentially curative gene therapies. Given the wide geographic distribution of SCD, with a major presence in Africa, it is imperative that new medicines are designed to meet the specific needs of persons with SCD everywhere. Target product profiles (TPPs) detail the desired attributes of new medicines and serve as a guide for drug developers. To support research efforts for curative treatments for SCD, we mobilized a large multi-disciplinary expert group to generate consensus-driven TPPs for and SCD gene therapies, utilizing a modified Delphi methodology supplemented with virtual workshops. The main findings are TPPs that describe 20 minimal and optimal criteria for novel gene therapy products in categories of scope (3 criteria), performance/safety (11 criteria), manufacturing (4 criteria), and administration (2 criteria). TPPs for and products differed in some performance/safety criteria and all criteria pertaining to manufacturing and administration. These outputs will ideally support development of durable treatments that are safe, efficacious, and practical for persons with SCD in global settings.
用于治疗镰状细胞病(SCD)的治疗创新正处于历史顶峰,其特点是药物发现、开发和商业化格局中包括了具有潜在治愈能力的基因疗法。鉴于SCD在全球广泛分布,在非洲尤为突出,设计新药以满足各地SCD患者的特定需求至关重要。目标产品概况(TPP)详细说明了新药所需的属性,并为药物开发者提供指导。为了支持SCD治愈性治疗的研究工作,我们动员了一个大型多学科专家组,采用改进的德尔菲方法并辅以虚拟研讨会,以达成关于SCD基因疗法的共识驱动型TPP。主要结果是TPP描述了新型基因治疗产品在范围(3项标准)、性能/安全性(11项标准)、生产(4项标准)和给药(2项标准)类别中的20项最低和最佳标准。用于 和 产品的TPP在一些性能/安全标准以及所有与生产和给药相关的标准方面存在差异。这些产出将理想地支持开发出对全球环境中的SCD患者安全、有效且实用的持久治疗方法。