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Trial · NCT02837198

Study of FYU-981 in Hyperuricemia (Effect on Two Hyperuricemic Types)

NCT02837198, Phase 2, Completed, Fuji Yakuhin Co., Ltd.

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Study of FYU-981 in Hyperuricemia (Effect on Two Hyperuricemic Types). Trials, record NCT02837198. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02837198

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Trial

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

Title
Study of FYU-981 in Hyperuricemia (Effect on Two Hyperuricemic Types)
NCT number
NCT02837198
Status
Completed
Phases
Phase 2
Enrollment
24 participants, actual
Lead sponsor
Fuji Yakuhin Co., Ltd.
Conditions
Hyperuricemia
Interventions
FYU-981, Topiroxostat
First posted
2016-07-19
Last updated
2018-08-21

Source ClinicalTrials.gov

Registered outcomes14

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

ListOutcomeTime frameDescription
PrimaryPharmacodynamics (Amount of uric acid excreted in urine)1-, 2-, 3-, 4-, 5-, 6-,7-,8- and 9-day
PrimaryPharmacodynamics (Renal clearance of uric acid)1-, 4- and 7-day
PrimaryPharmacodynamics (Fractional uric acid excretion)4- and 7-day
PrimaryPharmacodynamics (Maximum delta effective uric acid concentration)1-, 2-, 3-, 4-, 5-, 6- and 7-day
PrimaryPharmacodynamics (Delta area under the serum uric acid concentration-time curve)1-, 4- and 7-day
SecondaryPharmacokinetics (Cmax: Maximum plasma concentration)1-, and 7-day
SecondaryPharmacokinetics (Cmin: Minimum plasma concentration)1-, 2-, 3-, 4-, 5-, 6- and 7-day
SecondaryPharmacokinetics (Tmax: Time to reach the peak plasma concentration)1-, and 7-day
SecondaryPharmacokinetics (T1/2: Elimination half-life of plasma concentration)1-, and 7-day
SecondaryPharmacokinetics (AUC: Area under the plasma concentration-time curve)1-, and 7-day

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
31734820DERIVED

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.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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/NCT02837198

GET https://conductscience.org/api/trials/v1/NCT02837198/registered