Status:
TERMINATED
A Study to Investigate the Absorption, Metabolism and Excretion of Talampanel
Lead Sponsor:
Teva Branded Pharmaceutical Products R&D, Inc.
Collaborating Sponsors:
Covance
Conditions:
Healthy
Eligibility:
MALE
18-55 years
Phase:
PHASE1
Brief Summary
The purpose of this study is to characterize the chemical breakdown and excretion of talampanel and its break down products in plasma, feces, and urine of healthy human volunteers.
Eligibility Criteria
Inclusion
- Males, between 18 and 55 years of age, inclusive
- Body Mass Index range 18.0 to 30.0 kg/m2, inclusive
- Have NAT2 slow or rapid acetylator genotype
- In good health as determined by the investigator
- Negative test for selected drugs of abuse at screening
- Negative screens for Hepatitis B, Hepatitis C and HIV
- Sterile or agrees to use an approved method of contraception from Check-in until 45 days following Clinic Discharge
- Able to comprehend and willing to sign an Informed Consent Form
- Have 1 to 2 bowel movements per day
Exclusion
- Significant history or clinical manifestation of any significant metabolic, allergic, skin, liver, kidney, blood, heart or blood vessel, digestive system, brain or psychiatric disorder
- History of significant hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance
- History of stomach or intestinal surgery or resection
- History or presence of an abnormal ECG,
- History of clinically significant alcohol or drug use within 1 year prior to Check-in
- Participation in more than 1 other radiolabeled investigational study drug trial within 12 months prior to Check-in
- Exposure to significant radiation within 12 months prior to Check-in -Use of any tobacco- or nicotine-containing within 6 months prior to Check- in
- Use of any drugs which may interact with the study drug within 30 days prior to Check-in
- Participation in any other investigational study drug trial in which receipt of an investigational study drug occurred within 30 days prior to Check-in
- Use of any prescription medications/products within 14 days prior to Check in
- Use of any over-the-counter, non-prescription drugs within 7 days prior to Check-in
- Use of grapefruit or grapefruit-containing foods or beverages within 7 days prior to Check-in
- Use of alcohol- or caffeine-containing foods or beverages within 72 hours prior to Check-in
- Donation of blood from 30 days prior to Screening through Study Completion, inclusive, or of plasma from 2 weeks prior to Screening through Study Completion
- Receipt of blood products within 2 months prior to Check-in
- Any acute or chronic condition that would limit the subject's ability to complete and/or participate in this clinical study
Key Trial Info
Start Date :
May 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2009
Estimated Enrollment :
10 Patients enrolled
Trial Details
Trial ID
NCT00868361
Start Date
May 1 2009
End Date
September 1 2009
Last Update
September 16 2009
Active Locations (1)
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1
Covance Clinical Pharmacology Inc.
Madison, Wisconsin, United States, 53704