RecruitingNot ApplicableNCT06098742

Comparative Pharmacodynamics and Pharmacodynamics Equivalence of Antareit 800 mg/10 ml Oral Suspension and Riopan 800 mg Chewable Tablets in Healthy Volunteers

An Open-label, Randomized, Crossover Study to Investigate the Comparative Pharmacodynamics and Pharmacodynamics Equivalence of Antareit 800 mg/10 ml Oral Suspension and Riopan 800 mg Chewable Tablets in Healthy Volunteers.


Sponsor

Valenta Pharm JSC

Enrollment

50 participants

Start Date

Apr 25, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Comparative study of the pharmacodynamic parameters and pharmacodynamic equivalence (bioequivalence) of drug Antareit 800 mg/10 ml oral suspension and drug Riopan 800 mg chewable tablets in healthy volunteers.


Eligibility

Min Age: 18 YearsMax Age: 45 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Antareit for people with acid-dependent diseases of the gastrointestinal tract, heartburn, and other related conditions. The study is currently recruiting participants at 2 locations. People eligible for this study include aged 18 Years to 45 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGAntareit

A single dose of T or R drug in each of 2 periods of the study 2 h prior to food intake


Locations(2)

Llc "Certa Clinic"

Moscow, Russia

Limited Liability Company "Research Center Eco-Safety"

Saint Petersburg, Russia

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NCT06098742


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