Related Experiment Video
Updated: Nov 2, 2025

Assessing Specificity of Anticancer Drugs In Vitro
Published on: March 23, 2016
Factors Influencing Classifications of Safety Specifications in a Risk Management Plan for Antineoplastic Agents
Asami Ezaki1, Akihiro Hirakawa2, Hideki Hanaoka1,3
1Department of Regulatory Science of Medicine, Graduate School of Medicine, Chiba University, Chiba, Japan.
Abstract:
A risk management plan (RMP) has an important role in assuring the optimal benefit-risk balance of a drug throughout its life cycle. However, no clear standards have been established for differentiating risk classification between "important identified risks" and "important potential risks". This study was a review and descriptive analysis for Japanese RMPs with a focus on antineoplastic agents to identify effective factors to discriminate an important identified risk from an important potential risk. Analysis based on 51 RMPs, reporting 310 important identified risks and 72 important potential risks, revealed significant associations between selection of the risk classification and several factors, including severe cases, actual cases in the Japanese population, availability of confirmatory trial data, and incidence of adverse events. Trend of the association was also found for discontinuation cases and immune-oncology agents [IO (drug type)]. These results suggest that consideration of these factors may be useful for coherent risk classification in creating a RMP.
More Related Videos
Related Concept Videos
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast,...
Drug Regulation
Mutagenicity and Carcinogenicity
Clinically Relevant Drug Product Specifications: Methods of Establishment
Drug Classes and Categories
Chemotherapy-Induced Nausea and Vomiting: Neurokinin-1 Receptor Antagonists

