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Trial · NCT03185793

Dose-finding and Safety Study of SHR4640 in Subjects With Hyperuricemia

NCT03185793, Phase 2, Completed, Jiangsu HengRui Medicine Co., Ltd.

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Dose-finding and Safety Study of SHR4640 in Subjects With Hyperuricemia. Trials, record NCT03185793. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03185793

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Dose-finding and Safety Study of SHR4640 in Subjects With Hyperuricemia
NCT number
NCT03185793
Status
Completed
Phases
Phase 2
Enrollment
198 participants, actual
Lead sponsor
Jiangsu HengRui Medicine Co., Ltd.
Conditions
Hyperuricemia
Interventions
Placebo, SHR4640, benzbromarone
First posted
2017-06-14
Last updated
2019-08-07

Source ClinicalTrials.gov

Registered outcomes9

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryProportion of subjects with a serum uric level≤360μmol/l.Week 5
SecondaryActual change from baseline in serum uric level.Week 5
SecondaryPercentage change from baseline in serum uric level .Week 5
SecondaryRate of gout flares requiring treatment.Up to week 5
SecondaryIncidence of gout flares requiring treatment.Up to week 5
SecondaryProportion of subjects with a serum uric level≤360μmol/lAt week1, 2, 3 and 4
SecondaryProportion of subjects with a serum uric level consistent ≤360μmol/lAt week 3, 4 and 5
SecondaryActual change from baseline in serum uric levelAt week 1, 2, 3 and 4
SecondaryPercentage change from baseline in serum uric levelAt week 1, 2, 3 and 4

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
33693494DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT03185793

GET https://conductscience.org/api/trials/v1/NCT03185793/registered