Expired Study
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Austin, Texas 78759


Purpose:

The purpose of this study is to determine the pharmacokinetics, safety, and tolerability of different baclofen formulations.


Criteria:

Inclusion Criteria: - Between the ages of 18 and 65 years - Body mass index of 19 to 30 kg/m2 at screening - If subject is female and of childbearing potential, she must agree to use an acceptable method of contraception for the duration of the study Exclusion Criteria: - Pregnancy and/or currently breastfeeding - Clinical significant medical condition or observed abnormalities - Acute gastrointestinal disorder or history of chronic gastrointestinal disease or surgery - Participation in a clinical trial within 30 days before screening - Known intolerance and/or hypersensitivity to baclofen or its excipients - Use of alcohol-, caffeine-, or xanthine-containing products - Clinically significant illness within 30 days of first study drug administration - Dietary restrictions that conflict with required study meals


NCT ID:

NCT00802035


Primary Contact:

Principal Investigator
Frederick A. Bieberdorf, MD, CPI
CEDRA Clinical Research, LLC


Backup Contact:

N/A


Location Contact:

Austin, Texas 78759
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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