Dexpramipexole and Warfarin Drug Drug Interaction (DDI) Study

Phase 1

Completed

• Conditions: Healthy Volunteers
• Interventions: Drug: Dexpramipexole; Drug: Warfarin

• Registration Number: NCT01597310
• Lead Sponsor: Knopp Biosciences

Brief Summary

This study will assess the effect of dexpramipexole on the pharmacokinetics (PK) of the CYP2C9 probe substrate warfarin in healthy volunteers.

Detailed Description

This is a single center open label study to assess the effect of Dexpramipexole on the PK of Warfarin in Healthy Volunteers. The goals of this study are as follows: to assess the effect of dexpramipexole on the pharmacodynamics (PD) of warfarin, to assess the safety and tolerability of dexpramipexole when administered alone, and with warfarin, and to assess the PK of dexpramipexole when administered alone; to explore the influence of genetic variation on the PK and international normalized ratio (INR) of warfarin when administered alone, and with dexpramipexole; and to explore the influence of genetic variation on the PK of dexpramipexole when administered alone.

Study Timeline

• Study Start: 2012-05
• Study First Submitted: 2012-05-10
• Study First Submitted QC: 2012-05-10
• Study First Posted: 2012-05-14
• Primary Completion: 2012-07
• Study Completion: 2012-07
• Status Verified: 2014-11
• Last Update Submitted: 2014-11-24
• Last Update Posted: 2014-11-25

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 15

Inclusion Criteria

• Subjects who, in the opinion of the investigator, are healthy as determined by medical history, physical examination, and 12 Lead ECG.
• Adult males/females aged 18 to 55 years inclusive.
• Male and female subjects of childbearing age must practice effective contraception during the study and up to 90 days after their last dose of study drug.

Exclusion Criteria

• History of malignant disease, including solid tumors and hematologic malignancies.
• Clinically significant current active infection or serious infection.
• History of gastrointestinal bleeding, peptic ulcer disease, hemorrhoids or epistaxis.
• Personal or family history of any bleeding disorder, and/or coagulation profile results outside of normal limits.
• Known allergy or hypersensitivity to warfarin.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Dexpramipexole	Dexpramipexole	150 mg BID Treatment Period 2
Warfarin	Warfarin	25 mg Warfarin, Treatment Period 1 \& Treatment Period 2

Primary Outcome Measures

Name	Time	Method
PK parameters of dexpramipexole including but not limited to AUC: area under the plasma-concentration time curve over a specified time period and Cmax: Maximum observed plasma concentration	pre-dose and at 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8 and 12 hours after administration of the morning dexpramipexole dose on Day 1 and Day 12 of Period 2
Determination of the effect of dexpramipexole on the pharmacokinetics (PK) parameters of the CYP2C9 probe substrate warfarin including: AUC: area under the plasma-concentration time curve over a specified time period and Cmax: Maximum observed plasma c	pre-dose and at 0.5, 1, 2, 3, 4, 6, 8, 12, 24, 48, 72, 96 and 144 hours after warfarin administration in each dosing period

Trial Locations

Locations (1)

Research Site; 🇺🇸 Overland Park, Kansas, United States