Evidence map›Paper›PMID 36098470›Full record

Trial reportBritish journal of clinical pharmacology2023

A single-centre, open-label, single-arm, fixed-sequence pharmacokinetic study of SHR3680 on repaglinide and bupropion in prostate cancer patients.

Tao Dai, Zhenzhou Xu, Liang Huang, Yike Wang, Gongqian Zeng, Mingji Ye, Kan Liu, Fuhua Zeng, Shusuan Jiang, Weiqing Han and 1 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in British journal of clinical pharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 31% of its field
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

6 citing papers in PubMed, 4 citations in OpenAlex.

  1. Trial
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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

11 authors at 2 institutions in 1 country.

Tao DaiUrology Surgery Department, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.ORCID 0000-0001-8251-4088
Zhenzhou XuUrology Surgery Department, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Liang HuangUrology Surgery Department, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Yike WangDepartment of Clinical Pharmacology, Jiangsu Hengrui Pharmaceuticals Co., Ltd., Shanghai, China.
Gongqian ZengUrology Surgery Department, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Mingji YeUrology Surgery Department, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Kan LiuUrology Surgery Department, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Fuhua ZengUrology Surgery Department, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Shusuan JiangUrology Surgery Department, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Weiqing HanUrology Surgery Department, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Jingying CaoDepartment of Medicine Clinical Laboratory, The Third Xiangya Hospital of Central South University, Changsha, China.
Central South University · CNJiangsu Hengrui Medicine (China) · CN

Funding

Jiangsu Hengrui Pharmaceuticals Co., Ltd.
6 · The paper itself

Abstract

To evaluate the pharmacokinetic effects of SHR3680 on repaglinide and bupropion and its metabolite hydroxybupropion.

methodsA single-centre, open-label, single-arm, fixed-sequence clinical trial in 18 patients with prostate cancer.

resultsAfter a single oral dose of 0.5 mg repaglinide and SHR3680, geometric mean peak plasma concentration (C

conclusionCoadministration of SHR3680 with repaglinide or bupropion significantly shortened the elimination half-lives, significantly increased the apparent clearance rate, and significantly decreased the in vivo exposure of repaglinide, bupropion and hydroxybupropion compared with single administration of repaglinide or bupropion.

Indexed as

BupropionProstatic NeoplasmsArea Under CurveCarbamatesCross-Over StudiesHumansMalePiperidinesBupropionCarbamateshydroxybupropionPiperidinesrepaglinidebupropionpharmacokineticsprostate cancerrepaglinideSHR3680

Identifiers

PMID36098470
PMCPMC10092624
OpenAlexW4295366923

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.