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NCT02190786

Phase II Exploratory Clinical Study of KUX-1151

Completed Phase 2 Last updated 16 October 2015
What this trial tests

Phase 2 trial testing KUX-1151 in Hyperuricemia. Completed.

Quick facts

Lead sponsorKissei Pharmaceutical Co., Ltd.
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Primary completion1 March 2015
Sites1 location across Japan

Drugs / interventions tested

Conditions studied

Sponsor

Kissei Pharmaceutical Co., Ltd. — full company profile →

Who can join

Adults 20 to 64, any sex, with Hyperuricemia. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this study is to investigate the efficacy, safety and pharmacokinetics of multiple oral administration of KUX-1151 in patients with hyperuricemia including gout.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. SLC transporters as therapeutic targets: emerging opportunities.
    Lin L, Yee SW, Kim RB, Giacomini KM. · · 2015 · cited 653× · PMID 26111766 · DOI 10.1038/nrd4626

Verify or expand the search:

Other recruiting trials for Hyperuricemia

Currently open trials in the same condition.

Other Kissei Pharmaceutical Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02190786.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing