Tacrine Effects on Cocaine Self-Administration and Pharmacokinetics

Cocaine Dependence Clinical Trial

Official title:

Tacrine Effects on Cocaine Self-Administration and Pharmacokinetics

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01406522
• Other study ID #: R21DA029787
• Status: Withdrawn
• Phase: Phase 2
• First received: July 28, 2011
• Last updated: December 17, 2013
• Start date: October 2012
• Est. completion date: November 2013

Study information

• Verified date: December 2013
• Source: Midwest Biomedical Research Foundation
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

No medications are currently available for treatment of psychostimulant addiction, a compulsive preoccupation with use of cocaine and related compounds. Tacrine, a medication that is currently prescribed for Alzheimer's disease, can decrease the amount of cocaine injections that laboratory animals choose to inject by vein. This project will determine if tacrine can also decrease cocaine-motivated behavior for human subjects in a laboratory setting.

Description:

Background Reinforcing effects of cocaine are believed to arise through release of dopamine (DA) at the nucleus accumbens by neurons in the ventral tegmental area. Activation of cholinergic receptors on the cell bodies of these neurons can enhance DA release. Elevated levels of acetylcholine (ACh) in the nucleus accumbens may also serve to inhibit appetitive behaviors. Cholinesterase inhibitors such as tacrine increase synaptic levels of ACh by preventing its inactivation by acetylcholinesterase (AChE) or butyrylcholinesterase (BuChE), and can improve learning and memory. In animals, cholinesterase inhibitors can attenuate cocaine self-administration and conditioned place preference. Tacrine is a centrally acting, reversible inhibitor of AChE and BuChE that is approved for treatment of Alzheimer's disease. In addition to its effects on the cholinergic system, tacrine can potentiate the actions of monoamines, including DA. Although use of tacrine has declined because of requirements for monitoring of potential liver toxicity and pharmacokinetics that necessitate multiple daily doses, it is more potent than other cholinesterase inhibitors in attenuating cocaine self-administration in animals. Pretreatment with tacrine can produce long-lasting reductions in cocaine-reinforced behavior in rats, described as persistent attenuation (cocaine self-administration is decreased by more than 80% over a period of three days during which no additional cholinesterase inhibitor is administered, see Figure 1). No previous studies have evaluated whether tacrine can modify the effects of cocaine in humans.

Rationale To our knowledge, tacrine is the only compound that can produce persistent attenuation in rats treated with clinically relevant doses. If similar effects were observed in humans, this would lead to an important paradigm shift for substance abuse treatment, in that large reductions in cocaine-reinforced behavior could be produced without the need for continuous dosing with a medication. This scenario could remove the requirement for continued compliance with oral dosing in some patients with its associated potential for toxicity.

Specific Aims:

1. Evaluate whether tacrine treatment causes persistent attenuation of cocaine-reinforced behavior in humans.

2. Determine the effectiveness of pretreatment with tacrine in attenuating cocaine-induced craving.

3. Evaluate plasma levels of cocaine and characterize the bioavailability of tacrine in individual patients.

Methods This is a randomized, double-blind, double-dummy, placebo-controlled, inpatient, single-center, parallel-group evaluation of the potential for oral tacrine to modify cocaine self-administration, cocaine-induced craving, and the pharmacokinetics of cocaine and tacrine. To evaluate the occurrence of persistent attenuation, the subjective and reinforcing effects of intravenous cocaine will be determined during oral treatment and three days following its discontinuation.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: November 2013
• Est. primary completion date: September 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 21 Years to 50 Years

Eligibility

Inclusion Criteria:

• Meets DSM-IV-TR criteria for cocaine abuse or dependence, with at least one cocaine-positive urine specimen within the six weeks prior to enrollment.

• Has used cocaine for a duration of at least 6 months, with at least weekly use during the last 30 days by a rapid route of administration (either smoked or intravenous injection).

• Is male or female, between 21 and 50 years old.

Exclusion Criteria:

• Has a history of a medical adverse reaction to cocaine or other psychostimulants, including loss of consciousness, chest pain, cardiac ischemia, or seizure.

• Has any current Axis I psychiatric disorder other than drug abuse or dependence.

• Meets DSM-IV-TR criteria for dependence on opiates, benzodiazepines, alcohol, or other sedative-hypnotics.

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Cocaine Dependence

Intervention

Drug:
• Oral tacrine
Tacrine, 160 mg per day, four times daily
• Oral placebo
Microcrystalline cellulose

Locations

Country	Name	City	State
United States	Kansas City VA Medical Center	Kansas City	Missouri

Sponsors (1)

Lead Sponsor	Collaborator
Midwest Biomedical Research Foundation

Country where clinical trial is conducted

United States, 

References & Publications (2)

Grasing K, He S, Yang Y. Dose-related effects of the acetylcholinesterase inhibitor tacrine on cocaine and food self-administration in rats. Psychopharmacology (Berl). 2008 Jan;196(1):133-42. Epub 2007 Oct 5. — View Citation

Grasing K, He S, Yang Y. Long-lasting decreases in cocaine-reinforced behavior following treatment with the cholinesterase inhibitor tacrine in rats selectively bred for drug self-administration. Pharmacol Biochem Behav. 2009 Nov;94(1):169-78. doi: 10.1016/j.pbb.2009.08.004. Epub 2009 Aug 19. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Decreased cocaine-reinforced behavior	participants will make a series of choices between vouchers with an ascending monetary value and intravenous injections of cocaine	Day 9 of treatment	No
Secondary	Changes in cocaine pharmacokinetics	Plasma levels of cocaine and metabolites will be determined by liquid chromatography-tandem mass spectrometry	Day 9 of treatment	No

External Links

•   Priniciple Investigator Background
•   Sponsor