A Phase I Study in Healthy Volunteers to Assess Safety of BMS747158
NCT ID: NCT00707499
Last Updated: 2020-11-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
13 participants
INTERVENTIONAL
2007-09-30
2008-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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1
BMS747158
Single dose administration.
Interventions
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BMS747158
Single dose administration.
Eligibility Criteria
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Inclusion Criteria
* BMI 18-30 kg/m2
* No active or chronic illnesses
* If female: not pregnant, use of birth control or not of child-bearing potential
Exclusion Criteria
* Any neurological disorder
* GI disease within 3 months
* Recent infection
* Major surgery within 4 weeks
* Donation of blood within 4 weeks
* Blood transfusion within 4 weeks
* Recent history drug/alcohol abuse
* Head trauma
* Significant screening ECG, EEG, lab tests, physical exam and vital signs abnormalities
* Prescription or OTC drugs within 2 weeks
* Exposure to any other investigational drug/device within 6
18 Years
40 Years
ALL
Yes
Sponsors
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Lantheus Medical Imaging
INDUSTRY
Responsible Party
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Principal Investigators
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Jamshid Maddahi, MD
Role: PRINCIPAL_INVESTIGATOR
University of California, Los Angeles
Locations
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UCLA Medical Center
Los Angeles, California, United States
Countries
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Other Identifiers
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BMS747158-101
Identifier Type: -
Identifier Source: org_study_id