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โ† Trials
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Post-Marketing Surveillance to Evaluate the Safety and Effectiveness of Zastaprazan Citrate

Recruitingn/aAges 19 Years - anyAllJeil Pharmaceutical Co., Ltd.
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In plain words

What the trial is, and whether it could suit you

This post-marketing surveillance aims to evaluate the safety and effectiveness of zastaprazan citrate administered in Korean patients receiving the drug in accordance with the approved prescribing information.

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๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Patients who receive their first prescription for zastaprazan citrate in accordance with the approved prescribing information after execution of the study agreement * Patients who have received an explanation of the study and voluntarily signed the informed consent form. Exclusion Criteria: * Patients with hypersensitivity or a history of hypersensitivity to zastaprazan citrate or any component of the product. * atients currently receiving products containing atazanavir, nelfinavir, or rilpivirine. * Patients who are pregnant or breastfeeding. * Patients with hereditary disorders such as galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption. This exclusion criterion does not apply to the orally disintegrating tablet formulation.
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What it tests

  • zastaprazan citrate
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Where

1 site
Seoul National University BORAMAE Medical Center
Seoul, South Korea
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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