Clinical Trial for the Comparative Evaluation of Acid Suppression and Symptom Management of Gastroesophageal Reflux Disease With the Administration of Tegoprazan or Pantoprazole

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorCarnot Laboratories

About this trial

The objective of this clinical trial is to compare which of the two drugs best resolves symptoms in patients diagnosed with erosive and non-erosive gastroesophageal reflux disease, adult males and females. The main question is What is the proportion of patients with resolution of the main symptoms of gastroesophageal reflux disease at four weeks of treatment with pantoprazole vs tegoprazan.

Eligibility criteria

Qualifiers

With endoscopic diagnosis of GERD or NERD (endoscopy ≤ 15 days old)

With positive impedance pHmetry results (pHmetry ≤ 15 days old)

With recurrent symptoms of heartburn and regurgitation for a previous period ≥ 3 months old

Disqualifiers

With known hypersensitivity to tegoprazan, pantoprazole, or any of the components of each formulation

Subjects with concomitant administration of atazanavir, nelfinavir or rilpivirine

Nephropathic and/or hepatopathic subjects (including non-alcoholic hepatitis)

Subjects with upper gastrointestinal tract bleeding

Trial design

Treatments tested in this trial

  • Tegoprazan
  • Pantoprazole

Treatment groups

128 Participants
are divided into 4 treatment groups

Sponsors and collaborators