Vahle John L, Dybowski Joe, Graziano Michael, Hisada Shigeru, Lebron Jose, Nolte Thomas, Steigerwalt Ronald, Tsubota Kenjiro, Sistare Frank D
Lilly Research Laboratories, Indianapolis, IN, United States.
Alnylam Pharmaceuticals, Cambridge, MA, United States.
Front Toxicol. 2024 May 23;6:1377990. doi: 10.3389/ftox.2024.1377990. eCollection 2024.
Industry representatives on the ICH S1B(R1) Expert Working Group (EWG) worked closely with colleagues from the Drug Regulatory Authorities to develop an addendum to the ICH S1B guideline on carcinogenicity studies that allows for a weight-of-evidence (WoE) carcinogenicity assessment in some cases, rather than conducting a 2-year rat carcinogenicity study. A subgroup of the EWG composed of regulators have published in this issue a detailed analysis of the Prospective Evaluation Study (PES) conducted under the auspices of the ICH S1B(R1) EWG. Based on the experience gained through the Prospective Evaluation Study (PES) process, industry members of the EWG have prepared the following commentary to aid sponsors in assessing the standard WoE factors, considering how novel investigative approaches may be used to support a WoE assessment, and preparing appropriate documentation of the WoE assessment for presentation to regulatory authorities. The commentary also reviews some of the implementation challenges sponsors must consider in developing a carcinogenicity assessment strategy. Finally, case examples drawn from previously marketed products are provided as a supplement to this commentary to provide additional examples of how WoE criteria may be applied. The information and opinions expressed in this commentary are aimed at increasing the quality of WoE assessments to ensure the successful implementation of this approach.
国际人用药品注册技术协调会S1B(R1)专家工作组(EWG)的行业代表与药品监管机构的同事密切合作,制定了《国际人用药品注册技术协调会S1B致癌性研究指南》的增编,该增编允许在某些情况下进行证据权重(WoE)致癌性评估,而不是开展为期两年的大鼠致癌性研究。由监管机构组成的EWG子小组在本期发表了对在国际人用药品注册技术协调会S1B(R1)EWG主持下进行的前瞻性评估研究(PES)的详细分析。基于在前瞻性评估研究(PES)过程中获得的经验,EWG的行业成员编写了以下评论,以帮助申办者评估标准的证据权重因素,考虑如何使用新颖的研究方法来支持证据权重评估,并准备证据权重评估的适当文件以提交给监管机构。该评论还回顾了申办者在制定致癌性评估策略时必须考虑的一些实施挑战。最后,提供了一些来自先前上市产品的案例,作为本评论的补充,以提供更多关于如何应用证据权重标准的示例。本评论中表达的信息和观点旨在提高证据权重评估的质量,以确保该方法的成功实施。