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NCT06894992: TALENT

Tegoprazan And Lansoprazole Effectiveness in Bleeding Peptic Ulcer Treatment

Recruiting now NA Last updated 29 May 2025
What this trial tests

NA trial testing Tegoprazan in Peptic Ulcer Bleeding in 162 participants. Currently enrolling.

Timeline
1 May 2025
Primary endpoint
31 December 2025
31 December 2025

Quick facts

Lead sponsorMario Steffanus
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment162
Start date1 May 2025
Primary completion31 December 2025
Estimated completion31 December 2025
Sites2 locations across Indonesia

Drugs / interventions tested

Conditions studied

Sponsor

Mario Steffanus

Who can join

18 and older, any sex, with Peptic Ulcer Bleeding. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to compare the effects of tegoprazan vs lansoprazole in healing bleeding peptic ulcers. It will also teach about the safety of both modalities. The main questions it aims to answer are: How does the effectiveness of Tegoprazan compare with Lansoprazole in two weeks of healing rate bleeding peptic ulcer patients in the Indonesian population? Researchers will compare the drug tegoprazan to lansoprazole with a double-blind randomized control to see their effect on healing bleeding peptic ulcers. Participants will: Take drug tegoprazan 50 mg OD or lansoprazole 30 mg OD every day for 2 weeks Endoscopic examination at the beginning before treatment and after completion of treatment within 2 weeks Record of their adverse effect occurrence

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Tegoprazan

Trials testing the same drug.

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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/NCT06894992.

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