drugset / Trial / NCT06708520

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

NCT06708520

Phase 1 Recruiting 48 enrolled Noucor Health S.A.
Non-randomizedParallel-groupOpen-labelOther

Summary

The purpose of this study is to assess the PK, tolerability, and safety of rupatadine (10 mg) and its active metabolites in participants with renal impairment compared to matched control participants with normal renal function. The study duration will be up to 40 days, including Screening, Baseline, Study Period, and EOS visit assessments. Rupatadine 10 mg tablet will be administered as single dose.

Timeline

Start
2022-11-21
Primary completion
2025-07
Completion
2025-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Rupatadine Small molecule 10 mg