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Registered Clinical Trials Comprising Pregnant Women in China: A Cross-Sectional Study
Background: In this study, an investigation was conducted on clinical drug trials comprising pregnant women in China that provided data on the quantity, properties, source of funding, and geographical distribution regarding registration and post-marketing studies. Methods: We conducted a cross-secti...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016145/ https://www.ncbi.nlm.nih.gov/pubmed/35450038 http://dx.doi.org/10.3389/fphar.2022.850080 |
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author | Zhao, Yi Du, Guiping Luan, Xiaofei Yang, Hui Zhang, Qiongguang Zhang, Zhengfu Wang, Subiao |
author_facet | Zhao, Yi Du, Guiping Luan, Xiaofei Yang, Hui Zhang, Qiongguang Zhang, Zhengfu Wang, Subiao |
author_sort | Zhao, Yi |
collection | PubMed |
description | Background: In this study, an investigation was conducted on clinical drug trials comprising pregnant women in China that provided data on the quantity, properties, source of funding, and geographical distribution regarding registration and post-marketing studies. Methods: We conducted a cross-sectional descriptive study of clinical trials of pregnant women in China on 30 December 2021, and it was registered on the official Drug Clinical Trial Information Management Platform (ChiCTR) (http://www.chinadrugtrials.org.cn) established by the State Food and Drug Administration of China (Chinese FDA). Results: This study encompassed 72 registered trials (0.46%, 72/15,539) for data analysis. Of these trials, 43.1% of trials were started between 2013 and 2016, and nearly half of the trials (48.6%) were completed. Industries were listed as the primary sponsor for 95.8% trials. Economically developed eastern China and northern China, accounting for 69.5% of the 72 registered trials, were the most frequently identified study locations. Regarding study designs of these trials, more than half of the trials (70.8%) were randomized, 61.1% were a parallel assignment, 33.3% were phase 3, and half of the trials (54.2%) were open label. In total, 23 trials met the requirements after excluding trials of cancer and/or of postmenopausal women, accounting for 0.15% of the 15,539 registered trials in the ChiCTR websites. Of the 72 clinical trials, 54 drugs for 18 indications were included. Of these indications, the highest proportion of the trials is osteoporosis (27.8%), followed by cancer (22.2%), assisted reproduction (13.9%), and other indications (13.9%). Conclusion: This survey revealed a significant shortage of the development, evaluation, and safety trials of pregnancy-related drugs in China. Modifying or adding legislation and providing financial incentives may therefore encourage pharmaceutical companies to conduct additional clinical trials on pregnant women. |
format | Online Article Text |
id | pubmed-9016145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90161452022-04-20 Registered Clinical Trials Comprising Pregnant Women in China: A Cross-Sectional Study Zhao, Yi Du, Guiping Luan, Xiaofei Yang, Hui Zhang, Qiongguang Zhang, Zhengfu Wang, Subiao Front Pharmacol Pharmacology Background: In this study, an investigation was conducted on clinical drug trials comprising pregnant women in China that provided data on the quantity, properties, source of funding, and geographical distribution regarding registration and post-marketing studies. Methods: We conducted a cross-sectional descriptive study of clinical trials of pregnant women in China on 30 December 2021, and it was registered on the official Drug Clinical Trial Information Management Platform (ChiCTR) (http://www.chinadrugtrials.org.cn) established by the State Food and Drug Administration of China (Chinese FDA). Results: This study encompassed 72 registered trials (0.46%, 72/15,539) for data analysis. Of these trials, 43.1% of trials were started between 2013 and 2016, and nearly half of the trials (48.6%) were completed. Industries were listed as the primary sponsor for 95.8% trials. Economically developed eastern China and northern China, accounting for 69.5% of the 72 registered trials, were the most frequently identified study locations. Regarding study designs of these trials, more than half of the trials (70.8%) were randomized, 61.1% were a parallel assignment, 33.3% were phase 3, and half of the trials (54.2%) were open label. In total, 23 trials met the requirements after excluding trials of cancer and/or of postmenopausal women, accounting for 0.15% of the 15,539 registered trials in the ChiCTR websites. Of the 72 clinical trials, 54 drugs for 18 indications were included. Of these indications, the highest proportion of the trials is osteoporosis (27.8%), followed by cancer (22.2%), assisted reproduction (13.9%), and other indications (13.9%). Conclusion: This survey revealed a significant shortage of the development, evaluation, and safety trials of pregnancy-related drugs in China. Modifying or adding legislation and providing financial incentives may therefore encourage pharmaceutical companies to conduct additional clinical trials on pregnant women. Frontiers Media S.A. 2022-04-05 /pmc/articles/PMC9016145/ /pubmed/35450038 http://dx.doi.org/10.3389/fphar.2022.850080 Text en Copyright © 2022 Zhao, Du, Luan, Yang, Zhang, Zhang and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Zhao, Yi Du, Guiping Luan, Xiaofei Yang, Hui Zhang, Qiongguang Zhang, Zhengfu Wang, Subiao Registered Clinical Trials Comprising Pregnant Women in China: A Cross-Sectional Study |
title | Registered Clinical Trials Comprising Pregnant Women in China: A Cross-Sectional Study |
title_full | Registered Clinical Trials Comprising Pregnant Women in China: A Cross-Sectional Study |
title_fullStr | Registered Clinical Trials Comprising Pregnant Women in China: A Cross-Sectional Study |
title_full_unstemmed | Registered Clinical Trials Comprising Pregnant Women in China: A Cross-Sectional Study |
title_short | Registered Clinical Trials Comprising Pregnant Women in China: A Cross-Sectional Study |
title_sort | registered clinical trials comprising pregnant women in china: a cross-sectional study |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016145/ https://www.ncbi.nlm.nih.gov/pubmed/35450038 http://dx.doi.org/10.3389/fphar.2022.850080 |
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