Global Tuberculosis Programme, World Health Organization (WHO), Geneva, Switzerland.
Unité Mixte Internationale TransVIHMI, Unité mixte internationale 233, Institut de recherche pour le développement, Unité 1175, Université de Montpellier, Institut de Recherche pour le Développement (INSERM), Montpellier, France, Epidemiology and Population Health, Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.
Int J Tuberc Lung Dis. 2022 Apr 1;26(4):302-309. doi: 10.5588/ijtld.21.0667.
The WHO has developed target product profiles (TPPs) describing the most appropriate qualities for future TPT regimens to assist developers in aligning the characteristics of new treatments with programmatic requirements. A technical consultation group was convened by the WHO to determine regimen attributes with greatest potential impact for patients (i.e., improved risk/benefit profile) and populations (i.e., reduction in transmission and TB prevalence). The group categorised regimen attributes as 'priority´ or 'desirable´; and defined for each attribute the minimum requirements and optimal targets. Nine priority attributes were defined, including efficacy, treatment duration, safety, drug-drug interactions, barrier to emergence of drug resistance, target population, formulation, dosage, frequency and route of administration, stability and shelf life. Regimens meeting optimal targets were characterised, for example, as having superior efficacy, treatment duration of ≤2 weeks, and improved tolerability and safety profile compared with current regimens. The four desirable attributes included regimen cost, safety in special populations, treatment adherence and need for drug susceptibility testing in the index patient. It may be difficult for a single regimen to satisfy all characteristics so regimen developers may have to consider trade-offs. Additional operational aspects may be relevant to the feasibility and public health impact of new TPT regimens.
世界卫生组织(WHO)制定了目标产品概况(TPP),描述了未来结核分枝杆菌潜伏感染预防性治疗方案(TPP)最适宜的特性,以帮助研发人员调整新治疗方法的特点,使之符合规划要求。WHO 召集了一个技术咨询小组,确定了对患者(即改善风险/收益状况)和人群(即减少传播和结核病流行率)最具潜在影响的方案属性。该小组将方案属性归类为“优先”或“理想”;并为每个属性定义了最低要求和最佳目标。确定了九个优先属性,包括疗效、治疗持续时间、安全性、药物相互作用、耐药性出现的障碍、目标人群、剂型、剂量、频率和给药途径、稳定性和保质期。符合最佳目标的方案具有以下特点,例如,疗效优于目前的方案,治疗持续时间≤2 周,并且耐受性和安全性得到改善。四个理想的属性包括方案成本、特殊人群的安全性、治疗依从性和索引患者药物敏感性测试的需求。单一方案可能难以满足所有特性,因此方案研发人员可能不得不考虑权衡取舍。其他运营方面可能与新的结核分枝杆菌潜伏感染预防性治疗方案的可行性和公共卫生影响有关。