4.5 Review

Drugs currently in Phase II clinical trials for cocaine addiction

Journal

EXPERT OPINION ON INVESTIGATIONAL DRUGS
Volume 23, Issue 8, Pages 1105-1122

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1517/13543784.2014.915312

Keywords

addiction; clinical trials; cocaine; drug pipelines; therapeutics

Funding

  1. Victorian Government's Operational Infrastructure Support Program

Ask authors/readers for more resources

Introduction: There are no FDA-approved pharmacotherapies for treating cocaine addiction; thus, developing drugs to treat cocaine dependence is an unmet critical need. Fortunately, there are a number of drugs that are currently in Phase II clinical trial/s. This is due in part to the advances from in vivo imaging in humans which provided a roadmap of the neurochemistry of the cocaine-dependent brain. Most drugs currently in Phase II clinical trials attempt to modulate the disturbed neurochemistry in cocaine dependents to resemble those of healthy individuals. These predominantly modulate dopamine, serotonin, glutamate, GABA or noradrenaline signalling. Areas covered: This review summarizes the therapeutic potential of each drug as evidenced by clinical and preclinical studies. It also discusses their utility in terms of bioavailability and half-life. Expert opinion: Amphetamine salts and topiramate clearly stand out in terms of their potential efficacy in treating cocaine addiction. The efficacy of topiramate was closely associated with regular cognitive-behavioural therapy (CBT), which highlights the importance of a combined effort to promote abstinence and enhance retention via CBT. Cognitive/psychological screening appears necessary for a more symptom-based approach with more reasonable outcomes other than abstinence (e. g., improved quality of life) in treating cocaine addiction.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available