Objective To clarify the impact of Japan’s Clinical Trials Act (CTA), which was enacted in April 2018, on subsequent clinical trial activity through an analysis of Japanese registry data.Design Retrospective database study.Setting We extracted information on clinical intervention studies registered between 1 April 2018 and 30 September 2020 in the conventional University Hospital Medical Information Network Clinical Trials Registry (UMIN-CTR) and the new Japan Registry of Clinical Trials (jRCT). We collected and analysed information on registration dates, intervention types, funding, secondary sponsors and use of designated staff in multidisciplinary roles (research planning support, research administration, data management, statistical ana...
<div><p>Objectives</p><p>Despite increasing numbers of RCTs done in Japan, existing international da...
There are many differences between Asian regions in terms of the regulatory requirements and operati...
Background:In the United States (U.S.), human subject protection regulations, called “Common Rule”, ...
In April 2018, the Clinical Trials Act pertaining to investigator-initiated clinical trials was pass...
Background: Established on 1 June 2005, the University Hospital Medical Information Network Clinical...
Background : Enforcement of the 2018 Clinical Trials Act (CTA) in Japan resulted in strict and compl...
Background: The number of new noncommercial clinical studies conducted in Japan declined within the ...
In Japan, academic clinical trials do not generally need to be conducted under good clinical practic...
<p><sup>1</sup> The number of registries that provide data to the ICTRP has increased from nine to f...
This article evaluates the impact of the ICH E9 guideline Statistical Principles for Clinical Trials...
Full list of author information is available at the end of the articledrugs and medical devices (des...
In Japan, academic clinical trials do not generally need to be conducted under good clinical practic...
Abstract Background Large-scale clinical trials with thousands of participants are often needed to e...
The Japanese Ministry of Health, Labour and Welfare (JMHLW) introduced the Clinical Research Law1 in...
Despite increasing numbers of RCTs done in Japan, existing international databases fail to capture t...
<div><p>Objectives</p><p>Despite increasing numbers of RCTs done in Japan, existing international da...
There are many differences between Asian regions in terms of the regulatory requirements and operati...
Background:In the United States (U.S.), human subject protection regulations, called “Common Rule”, ...
In April 2018, the Clinical Trials Act pertaining to investigator-initiated clinical trials was pass...
Background: Established on 1 June 2005, the University Hospital Medical Information Network Clinical...
Background : Enforcement of the 2018 Clinical Trials Act (CTA) in Japan resulted in strict and compl...
Background: The number of new noncommercial clinical studies conducted in Japan declined within the ...
In Japan, academic clinical trials do not generally need to be conducted under good clinical practic...
<p><sup>1</sup> The number of registries that provide data to the ICTRP has increased from nine to f...
This article evaluates the impact of the ICH E9 guideline Statistical Principles for Clinical Trials...
Full list of author information is available at the end of the articledrugs and medical devices (des...
In Japan, academic clinical trials do not generally need to be conducted under good clinical practic...
Abstract Background Large-scale clinical trials with thousands of participants are often needed to e...
The Japanese Ministry of Health, Labour and Welfare (JMHLW) introduced the Clinical Research Law1 in...
Despite increasing numbers of RCTs done in Japan, existing international databases fail to capture t...
<div><p>Objectives</p><p>Despite increasing numbers of RCTs done in Japan, existing international da...
There are many differences between Asian regions in terms of the regulatory requirements and operati...
Background:In the United States (U.S.), human subject protection regulations, called “Common Rule”, ...