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To Assess the Safety and Tolerability of 7.5, 15 and 30 mg of Sublingual Lobeline. - 1

Information source: National Institute on Drug Abuse (NIDA)
ClinicalTrials.gov processed this data on August 20, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Amphetamine-Related Disorders

Intervention: Lobeline (Drug)

Phase: Phase 1

Status: Active, not recruiting

Sponsored by: National Institute on Drug Abuse (NIDA)

Official(s) and/or principal investigator(s):
Reese Jones, M.D., Principal Investigator, Affiliation: Langley Porter Psychiatric Institute


To assess the safety and tolerability of 7. 5, 15 and 30 mg of sublingual lobeline.

Clinical Details

Official title: Safety and Tolerability Study of Sublingual Lobeline

Study design: Primary Purpose: Diagnostic

Primary outcome: Safety

Detailed description: The primary objective of this study is to characterize the pharmacokinetics of three ascending doses of lobeline in normal volunteers.


Minimum age: 18 Years. Maximum age: 45 Years. Gender(s): Both.


Inclusion Criteria:

- Healthy individuals with a body mass index between 18 and 30.

- 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:

- Please contact the site for more information

Locations and Contacts

U of CA, San Francisco, San Francisco, California 94143, United States
Additional Information

Starting date: September 2004
Last updated: October 25, 2007

Page last updated: August 20, 2015

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