drugset / Trial / NCT06736340

Pharmacokinetics and Safety of Rupatadine in Participants With Hepatic Impairment Compared to Control Participants.

NCT06736340

Phase 1 Completed 26 enrolled Noucor Health S.A.
Non-randomizedParallel-groupOpen-labelOther

Summary

The purpose of this study is to assess the PK and safety of rupatadine (10 mg) and its active metabolites in participants with mild, moderate, or severe hepatic impairment compared to matched control participants with normal hepatic function. The study duration will be up to 38 days, including Screening, Baseline, Study Period, and EOS Visit assessments. Rupatadine 10 mg tablet will be administered as single dose.

Timeline

Start
2022-11-17
Primary completion
2025-04-09
Completion
2025-04-09

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Rupatadine Small molecule 10 mg

Indications

No indication recorded.