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NCT05886933

Study to Evaluate the Efficacy and Safety of FEXUCLUE Tablet

Completed Last updated 24 January 2025
What this trial tests

trial testing Fexuprazan Hydrochloride in Gastroesophageal Reflux Disease in 9,846 participants. Completed in 31 December 2024.

Timeline
22 May 2023
Primary endpoint
30 April 2024
31 December 2024

Quick facts

Lead sponsorDaewoong Pharmaceutical Co. LTD.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment9,846
Start date22 May 2023
Primary completion30 April 2024
Estimated completion31 December 2024
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Daewoong Pharmaceutical Co. LTD. — full company profile →

Who can join

Adults 19 to 75, any sex, with Gastroesophageal Reflux Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This observational study is a large-scale, prospective, and multi-institutional observational study. Patients from 19 to 75 years of age, will take a self-assessment (PRO) during the study period before and after administration of Pexuclue tablet.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Fexuprazan Hydrochloride

Trials testing the same drug.

Other recruiting trials for Gastroesophageal Reflux Disease

Currently open trials in the same condition.

Other Daewoong 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/NCT05886933.

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