Overview of the Premarketing and Postmarketing Requirements for Drugs Granted Japanese Conditional Marketing Approval
For drugs that are intended to fill unmet medical needs, such as the treatment of rare diseases or a subtype of cancer, it can take a long time to conduct confirmatory clinical trials due to limited patient availability. Delayed access to these drugs increases the risk of mortality of patients with...
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doaj-7e0ccc1ef038497ea486c90ec2cd22962021-06-18T13:27:20ZengWileyClinical and Translational Science1752-80541752-80622021-05-0114380681110.1111/cts.12898Overview of the Premarketing and Postmarketing Requirements for Drugs Granted Japanese Conditional Marketing ApprovalShunsuke Matsushita0Keisuke Tachibana1Tetsuya Kusakabe2Ryuichi Hirayama3Yasuo Tsutsumi4Masuo Kondoh5Graduate School of Pharmaceutical Sciences Osaka University Osaka JapanGraduate School of Pharmaceutical Sciences Osaka University Osaka JapanGraduate School of Medicine Osaka City University Osaka JapanGraduate School of Medicine Osaka University Osaka JapanGraduate School of Pharmaceutical Sciences Osaka University Osaka JapanGraduate School of Pharmaceutical Sciences Osaka University Osaka JapanFor drugs that are intended to fill unmet medical needs, such as the treatment of rare diseases or a subtype of cancer, it can take a long time to conduct confirmatory clinical trials due to limited patient availability. Delayed access to these drugs increases the risk of mortality of patients with these diseases. To address this issue, the Ministry of Health, Labour, and Welfare of Japan has decided to implement the Conditional Early Approval System with issuing the Ministry Notification in 2017. Drugs eligible for conditional early approval are those that are indicated for the treatment of a serious disease, have proven safety and efficacy, and cannot be examined easily by confirmatory clinical trials. When the benefit of immediate availability outweighs the risk of having less comprehensive data with which to confirm the clinical benefit of a product in the premarketing phase, products can be approved under the Conditional Early Approval System, accompanied by postmarketing regulatory requirements to manage postmarketing risks and, if needed, conduct postmarketing confirmatory clinical studies. Overview of the pre‐approval and post‐approval regulatory considerations will promote to more efficiently develop pharmaceutical products that fill unmet medical needs, leading to the prompt delivery of safe and effective drugs to patients who often have few therapeutic options available. As of March 2020, four drugs had been approved under the Conditional Early Approval System. In this review, we describe the premarketing and postmarketing requirements of these drugs and discuss the regulatory landscape around the Conditional Early Approval System.https://doi.org/10.1111/cts.12898 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shunsuke Matsushita Keisuke Tachibana Tetsuya Kusakabe Ryuichi Hirayama Yasuo Tsutsumi Masuo Kondoh |
spellingShingle |
Shunsuke Matsushita Keisuke Tachibana Tetsuya Kusakabe Ryuichi Hirayama Yasuo Tsutsumi Masuo Kondoh Overview of the Premarketing and Postmarketing Requirements for Drugs Granted Japanese Conditional Marketing Approval Clinical and Translational Science |
author_facet |
Shunsuke Matsushita Keisuke Tachibana Tetsuya Kusakabe Ryuichi Hirayama Yasuo Tsutsumi Masuo Kondoh |
author_sort |
Shunsuke Matsushita |
title |
Overview of the Premarketing and Postmarketing Requirements for Drugs Granted Japanese Conditional Marketing Approval |
title_short |
Overview of the Premarketing and Postmarketing Requirements for Drugs Granted Japanese Conditional Marketing Approval |
title_full |
Overview of the Premarketing and Postmarketing Requirements for Drugs Granted Japanese Conditional Marketing Approval |
title_fullStr |
Overview of the Premarketing and Postmarketing Requirements for Drugs Granted Japanese Conditional Marketing Approval |
title_full_unstemmed |
Overview of the Premarketing and Postmarketing Requirements for Drugs Granted Japanese Conditional Marketing Approval |
title_sort |
overview of the premarketing and postmarketing requirements for drugs granted japanese conditional marketing approval |
publisher |
Wiley |
series |
Clinical and Translational Science |
issn |
1752-8054 1752-8062 |
publishDate |
2021-05-01 |
description |
For drugs that are intended to fill unmet medical needs, such as the treatment of rare diseases or a subtype of cancer, it can take a long time to conduct confirmatory clinical trials due to limited patient availability. Delayed access to these drugs increases the risk of mortality of patients with these diseases. To address this issue, the Ministry of Health, Labour, and Welfare of Japan has decided to implement the Conditional Early Approval System with issuing the Ministry Notification in 2017. Drugs eligible for conditional early approval are those that are indicated for the treatment of a serious disease, have proven safety and efficacy, and cannot be examined easily by confirmatory clinical trials. When the benefit of immediate availability outweighs the risk of having less comprehensive data with which to confirm the clinical benefit of a product in the premarketing phase, products can be approved under the Conditional Early Approval System, accompanied by postmarketing regulatory requirements to manage postmarketing risks and, if needed, conduct postmarketing confirmatory clinical studies. Overview of the pre‐approval and post‐approval regulatory considerations will promote to more efficiently develop pharmaceutical products that fill unmet medical needs, leading to the prompt delivery of safe and effective drugs to patients who often have few therapeutic options available. As of March 2020, four drugs had been approved under the Conditional Early Approval System. In this review, we describe the premarketing and postmarketing requirements of these drugs and discuss the regulatory landscape around the Conditional Early Approval System. |
url |
https://doi.org/10.1111/cts.12898 |
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