Assessment of 2012 Bioequivalence Standards for Warfarin

Completed · Phase 1

Conditions studied: Healthy

In brief

The purpose of this study is to assess the 2012 bioequivalence statistical criteria for warfarin, a narrow therapeutic index drug, set forth in the draft guidance issued by the Food and Drug Administration (FDA).

Key facts

Study ID

NCT02574754

Run by

University of California, San Francisco

People needed

10

Starts

2016-05-01

Expected to finish

2019-02-01

Last updated by the study team

2019-08-05

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female aged 18-60 years
• Healthy adult without active medical problems or chronic diseases based on medical history, physical exam, and laboratory results
• BMI 18.5-32 kg/m2
• Ceased all medications 2 weeks prior to start of study and during study enrollment (includes drugs of abuse, prescription medications, and over-the-counter (OTC) medications [exception: acetaminophen])
• Maintain adequate birth control independent of hormonal contraceptive use throughout study
• Provide written informed consent to take part in and comply with the requirements of the study
• Speak, read, and understand English
• Avoid alcohol, caffeine, and orange juice from 6pm the night before the study day until the completion of the study day
• Avoid contact sports and/or other activities with significant risk of trauma injury for 7 days after each study day
• Do not eat food or consume beverages at least 8 hours before medication dosing
• Present with wild type VKORC1, VKORC-1639G>A and wild type CYP2C9 genotype

You may not qualify if…

• Subjects on prescription or chronic OTC medications (including hormonal contraceptives)
• Subjects with known allergy to warfarin
• Subjects with a history of or diagnosis of hemorrhagic tendencies or blood dyscrasias
• Subjects with liver failure or liver function tests (LFTs) > 2x upper limit normal
• Subjects with clinically significant elevations of international normalized ratio (INR), prothrombin time (PT), partial thromboplastin time (PTT), serum creatinine (Scr), blood urea nitrogen (BUN), or other screening laboratory tests as determined by study physician
• Subjects with hematocrit (Hct) < 30 mg/dL
• Subjects with history of GI bleed or peptic ulcer disease
• Subjects with recent history of trauma
• Subjects with recent history of or upcoming plan for surgery
• Subjects who smoke tobacco
• Subjects with ongoing alcohol use
• Subjects with ongoing illegal drug use
• Subjects who are pregnant, attempting to become pregnant, or lactating
• Subjects who are unable to maintain adequate birth control during the study
• Subjects who are unable to follow protocol instructions or criteria
• Subjects with genotypes that are not wild type VKORC1, VKORC-1639G>A and wild type CYP2C9

Where it is running

• University of California, San Francisco — San Francisco, California, United States

Full record on ClinicalTrials.gov

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