Bioequivalence Study Between Two Oral Formulations of Ibuprofen 800 mg Tablets Under Fed Conditions

A Randomized, Single-Dose, Two-Way Crossover Relative Bioavailability Study of Ibuprofen Tablet Formulations in Normal, Healthy Men and Women Following Standard Meal

Status

Completed

Phases

Phase 1

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00803946

Enrollment

Registered

2008-12-08

Start date

2003-11-30

Completion date

Unknown

Last updated

2012-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bioequivalency

Keywords

bioequivalency, ibuprofen

Brief summary

Compare the rate and extent of absorption of two oral formulations of Ibuprofen 800 mg Tablets, administered as a 1 x 800 mg tablet, under fed conditions.

Interventions

DRUGIbuprofen Tablets, 800 mg

Study design

Allocation

RANDOMIZED

Intervention model

CROSSOVER

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* healthy men or women, 18 years of age or older * body mass index between 19 and 30 * willing to participate and sign a copy of the informed consent form

Exclusion criteria

* history of allergy or hypersensitivity to ibuprofen * recent history of drug or alcohol addiction or abuse * pregnant or lactating women * use of tobacco products during the past 3 months * evidence of a clinically significant disorder or whose laboratory results were deemed to be clinically significant * receipt of any drugs as part of a research study within 30 days prior to study dosing

Design outcomes

Primary

Measure	Time frame
Bioequivalence was assessed on the pharmacokinetic variables Cmax, AUC,0-t, and AUC,0-infinity	—

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026