drugset / Trial / NCT05329454

To Evaluate the Food Effect and the Absorption Profile of Ibuprofen Modified-Release Tablets 800 mg

NCT05329454

Phase 1 Completed 30 enrolled Overseas Pharmaceuticals, Ltd.
RandomizedCrossoverOpen-labelTreatment

Summary

An open-label, randomized, 3-way crossover study to evaluate the pharmacokinetics of investigational product "Ibuprofen Modified-Release Tablets 800 mg" in comparison to the reference standard "Ibuprofen Regular-Release Tablets 600 mg/800 mg" in normal healthy volunteers Primary objective: To evaluate the food effect of IBUMR and its bioavailability of single and multiple doses compared with reference drugs in normal healthy volunteers. Secondary objectives: 1. To determine and compare the single and multiple dose PK profiles of IBUMR and reference drugs. 2. To identify the effect duration for IBUMR after dose administration by detecting ibuprofen concentrations in plasma. 3. To evaluate the safety profile of single and multiple doses of IBUMR.

Timeline

Start
2020-12-24
Primary completion
2021-02-06
Completion
2021-07-18

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ibuprofen Small molecule 600 mg
Subject Ibuprofen Small molecule 800 mg

Indications