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COMPLETEDPhase 1NCT00813670

Single and Multiple Ascending Dose Safety Study of XPF-001 in Healthy Volunteers

The purpose of this study is to assess the safety, tolerability and pharmacokinetics of single and multiple doses of XPF-001 in healthy volunteers. The effect of food on the pharmacokinetics of XPF-0...

Lead sponsor: Xenon Pharmaceuticals Inc.•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Xenon Pharmaceuticals Inc.

Age

18 - 60 years

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•Healthy subjects (Females of non-childbearing potential) with normal or clinically insignificant laboratory results, ECGs and physical examinations.

Exclusion Criteria

•Subjects with a presence or history of any clinically significant disease.
•Subjects who have participated in and investigational drug trial within 60 days of admission.
•Subjects who have used tobacco or nictoine products in the 1 month prior to admission
•Females who are pregnant or breastfeeding

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: September 14, 2009Terms

Trial snapshot

StatusCOMPLETED

PhasePHASE1

Enrollment64

Start dateNov 2008

Last updatedSep 14, 2009

Condition

Healthy Human Volunteers

Locations shown

Anapharm

Montreal, Quebec

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: September 14, 2009Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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