Effect of Antacid on Bioavailability of Febuxostat After Administration of a Febuxostat 80 mg Extended-Release Capsule

Completed · Phase 1

Conditions studied: Healthy Volunteers

In brief

The purpose of this study is to assess the effect of antacid administration, and its timing, on the bioavailability of a single dose of febuxostat extended-release (XR) 80 mg.

Key facts

Study ID

NCT02382640

Run by

Takeda

People needed

36

Starts

2015-03-01

Expected to finish

2015-05-01

Last updated by the study team

2016-04-29

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Is a healthy adult male or female aged 18 to 55 years, inclusive, by check-in (Day-1 of Period 1)
• Weighs at least 50 kg (110 pounds), and has a body mass index (BMI) between 18.0 kg/m\^2 to 30 kg/m\^2, inclusive at Screening.
• Has estimated glomerular filtration rate ≥90 mL/min

You may not qualify if…

• Any participant who meets any of the following criteria will not qualify for entry into the study:
• Has received any investigational compound within 30 days prior to the first dose of study medication.
• Has received febuxostat in a previous clinical study or as a therapeutic agent.
• Has a known hypersensitivity to any xanthine oxidase inhibitor, xanthine compounds or any component of the formulation of febuxostat tablets (see Package Insert) or to caffeine.
• Has a known hypersensitivity to aluminum, magnesium hydroxide, or any component of the formulation of antacid (Maalox Advanced Regular Strength or equivalent) (see Package Insert).
• Has a history of drug abuse (defined as any illicit drug use) or a history of alcohol abuse within 1 year prior to the Screening visit or is unwilling to agree to abstain from alcohol and drugs throughout the study. If female, the participant is pregnant or lactating or intending to become pregnant before, during, or within 30 days after participating in this study; or intending to donate ova during such time period.
• Has current or recent (within 6 months) gastrointestinal disease that would be expected to influence the absorption of drugs (ie, a history of malabsorption, esophageal reflux, peptic ulcer disease, erosive esophagitis frequent [more than once per week] occurrence of heartburn, or any surgical intervention [eg, cholecystectomy]).

Where it is running

• Study site — Austin, Texas, United States

Full record on ClinicalTrials.gov

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