To Assess the Safety and Tolerability of 7.5, 15 and 30 mg of Sublingual Lobeline. - 1
NCT ID: NCT00100074
Last Updated: 2017-01-11
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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UNKNOWN
PHASE1
8 participants
INTERVENTIONAL
2004-09-30
2005-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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DIAGNOSTIC
Interventions
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Lobeline
Eligibility Criteria
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Inclusion Criteria
* Willing and able to give written consent.
* Must have a negative drug test
* Females must have a negative pregnancy test prior to study drug administration
* Must have no medical contraindications as determined by routine testing
Exclusion Criteria
18 Years
45 Years
ALL
Yes
Sponsors
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National Institute on Drug Abuse (NIDA)
NIH
Principal Investigators
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Reese Jones, M.D.
Role: PRINCIPAL_INVESTIGATOR
Langley Porter Psychiatric Institute
Locations
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U of CA, San Francisco
San Francisco, California, United States
Countries
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Other Identifiers
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NIDA-CPU-0007-1
Identifier Type: -
Identifier Source: org_study_id
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