Evidence map›Paper›PMID 37484857›Full record

ArticleFrontiers in medicine2023

Trends in innovative pediatric drug development in China based on clinical trial registration data.

Wen-Wen Wu, Xing Ji, Xin-Shuang Mou, Xin-Yue Ma, Ya-Ting Huang, Jie-Ying Zhang, Jing-Xian Zhang, Xin-Rong Xie, Ning-Ying Mao, Jing Xu

Abstract read
In one paragraph

Article in Frontiers in medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Wen-Wen WuSchool of International Pharmaceutical Business, China Pharmaceutical University, Nanjing, Jiangsu, China.
Xing JiDepartment of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Xin-Shuang MouSchool of International Pharmaceutical Business, China Pharmaceutical University, Nanjing, Jiangsu, China.
Xin-Yue MaSchool of International Pharmaceutical Business, China Pharmaceutical University, Nanjing, Jiangsu, China.
Ya-Ting HuangSchool of International Pharmaceutical Business, China Pharmaceutical University, Nanjing, Jiangsu, China.
Jie-Ying ZhangSchool of International Pharmaceutical Business, China Pharmaceutical University, Nanjing, Jiangsu, China.
Jing-Xian ZhangSchool of International Pharmaceutical Business, China Pharmaceutical University, Nanjing, Jiangsu, China.
Xin-Rong XieSchool of International Pharmaceutical Business, China Pharmaceutical University, Nanjing, Jiangsu, China.
Ning-Ying MaoSchool of International Pharmaceutical Business, China Pharmaceutical University, Nanjing, Jiangsu, China.
Jing XuDepartment of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In China, the focus of drug research and development has gradually shifted from generic to innovative drugs. Using the Chinese Clinical Trials Registry and Information Transparency Platform, we retrospectively analyzed clinical trials of innovative pediatric drugs conducted in mainland China over the last decade. The goal of this work was to better understand the characteristics of and historical changes in innovative pediatric drug research and development (R&D) in China and to provide effective data support for policy makers and other stakeholders. This study included 198 innovative pediatric drug clinical trials. The data showed that, although some progress has been made in the R&D of innovative pediatric drugs in China, many factors limiting this progress still exist, such as concentrated R&D areas, inadequate pediatric participants, and unbalanced source distributions. The level of innovative pediatric drug R&D in China currently lags behind the global level and has not kept pace with anti-neoplastic drug R&D in China. To promote the innovative development of pediatric drugs in China, the Chinese government must develop an R&D supervision framework, improve the motivation and innovation capabilities of pharmaceutical companies, and optimize the source distribution between regions.

Indexed as

Chinese Clinical Trials Registry and Information Transparency Platformclinical trialinnovative pediatric drugpediatric populationresearch and development

Identifiers

PMID37484857
PMCPMC10359815

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.