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Bioequivalence of a Fixed Dose Combination Tablet Containing 200 mg Ibuprofen and 30 mg Pseudoephedrine-HCl Compared to RhinAdvil(R)(200 mg Ibuprofen and 30 mg Pseudoephedrine-HCl) as a Fixed Dose Combination Tablet Administered in Healthy Volunteers.

Phase 1
Completed
Conditions
Healthy
Interventions
Drug: Pseudoephedrine-HCl
Registration Number
NCT01170637
Lead Sponsor
Boehringer Ingelheim
Brief Summary

The objective of the current study is to demonstrate bioequivalence of a fixed dose combination tablet containing ibuprofen 200 mg and pseudoephedrine-HCl 30 mg (Test) and RhinAdvil® (Reference) a fixed dose combination tablet containing ibuprofen 200 mg and pseudoephedrine-HCl 30 mg following orally administration.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
47
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Ibuprofen 200 mgIbuprofenOral administration as a fixed dose combination tablet (RhinAdvil(R))
Pseudoephedrine-HCl 30 mgPseudoephedrine-HClOral administration as a fixed dose combination tablet (RhinAdvil(R))
Ibuprofen 200 mg BIIbuprofenOral administration as a fixed dose combination tablet (BI product)
Pseudoephedrine-HCl 30 mg BIPseudoephedrine-HClOral administration as a fixed dose combination tablet (BI product)
Primary Outcome Measures
NameTimeMethod
AUC0-tz (area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the time of last quantifiable time point)1 month
Cmax (maximum measured concentration of the analyte in plasma)1 month
Secondary Outcome Measures
NameTimeMethod
AUC0-* (area under the concentration-time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity) (*=infinity)1 month

Trial Locations

Locations (1)

1024.7.1 Boehringer Ingelheim Investigational Site

🇩🇪

Ingelheim, Germany

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