Evidence map›Paper›PMID 34268710›Full record

ArticleInvestigational new drugs2021

A critical appraisal of Japan's new drug approval process: a case study of FLT3-ITD inhibitor quizartinib.

Keisuke Kidoguch, Motoharu Shibusawa, Tetsuya Tanimoto

Abstract read
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In one paragraph

Article in Investigational new drugs, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Keisuke KidoguchSaga-Ken medical centre KOSEIKAN, Department of Hematology, Saga, Japan. keisuke.kidoguchi.md@gmail.com.ORCID 0000-0003-0712-0083
Motoharu ShibusawaDepartment of Hematology, Shinmatsudo Central General Hospital, Chiba, Japan.
Tetsuya TanimotoNavitas Clinic Kawasaki, Kanagawa, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the last two decades, simultaneous global development of novel drugs become more common by conducting multiregional clinical trials. However, regulatory authorities of different regions often make different decisions on the approvals of the same new drugs. We would like to discuss the appropriateness of Japanese regulatory approach through a case study of quizartinib, a novel anti-leukemia drug developed in Japan. The pivotal clinical trial "QuANTUM-R" conducted in 19 countries showed a modest increase in median overall survival with quizartinib than the conventional chemotherapy. However, because several critical defects in this trial were pointed out by the United States Food and Drug Administration (US FDA) and the European Medicines Agency (EMA), quizartinib has not been approved in the US and Europe to date. On the contrary, the regulatory authority of Japan gave a notice of approval to quizartinib as a "standard of care", and the country becomes the sole country that granted market authorization. In our paper, we provide more detailed discussion about the methodology for scientific evaluation of the new drug.

Indexed as

BenzothiazolesClinical Trials as TopicDrug Approvalfms-Like Tyrosine Kinase 3HumansJapanLeukemia, Myeloid, AcuteMulticenter Studies as TopicPhenylurea CompoundsProtein Kinase InhibitorsUnited StatesUnited States Food and Drug AdministrationBenzothiazolesfms-Like Tyrosine Kinase 3Phenylurea CompoundsProtein Kinase InhibitorsquizartinibAcute myeloid leukemiaFLT3QuizartinibRegulatory science

Identifiers

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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.