Pharmacokinetics Clinical Trial
Official title:
Pharmacodynamic and Pharmacokinetic Interactions Between Intravenous Cocaine and Acetazolamide or Quinine
Background:
- Scientists are studying medications that may be useful in treating cocaine addiction. It is
important in these studies to know whether study participants are always taking their
medications as directed. This study will look at two chemicals to see if they can be used to
determine whether participants are taking their medications as directed. Because
acetazolamide and quinine can be measured in plasma and urine, they are good test subjects
for this study. They will be given alone, and combined with intravenous cocaine.
Objectives:
- To see how they body handles acetazolamide and quinine alone, and when combined with
cocaine.
Eligibility:
- Individuals between 18 and 50 years of age who have smoked or used IV cocaine for at least
one year and at least three times per month during the three months prior to screening. Urine
test positive for cocaine within the prior 6 months
Design:
- Participants will be screened with a physical exam and medical history. Blood and urine
samples will also be collected.
- This study will involve a 12-day inpatient stay at the National Institutes of Health.
- On days 1, 5, and 10, participants will receive a dose of cocaine. Blood, urine, breath,
and saliva samples will be collected up to 18 times a day for up to about 24 hours.
- On days 2, 3, 4, and 5, participants will receive acetazolamide. Regular blood samples
will be collected on Day 4.
- Day 6 is a wash-out day with no drugs or blood tests.
- On days 7, 8, 9, and 10, participants will receive quinine. Regular blood samples will
be collected on Day 9.
- On day 11, blood, urine, breath, and saliva samples will be collected in the early
morning. Participants will be able to leave later in the day.
Background: Cocaine dependence is a public health concern worldwide, with no FDA-approved
pharmacological treatment for this condition. Thus, there is a need for controlled clinical
trials to evaluate potential new pharmacological treatments. Adherence to a medication regime
is a major factor in the success of treatment. In controlled clinical trials, medication
adherence is often monitored by measuring specific markers ingested with the medication. No
such markers are validated for use in studies of cocaine dependence treatment.
Objective: Evaluate the feasibility of oral acetazolamide and quinine as adherence markers in
trials of cocaine dependence treatment by determining their pharmacodynamic and
pharmacokinetic interactions with intravenous (IV) cocaine.
Study Population: Up to 30 healthy cocaine users aged 18-50 years who smoked or used IV
cocaine for at least one year and at least three times per month during the three months
prior to screening and had a positive urine test for cocaine within the last 6 months.
Experimental Design and Methods: Participants are admitted to a secure residential research
unit on and undergo baseline assessments on Day -1, receive training on Day 0, and receive
single doses of IV cocaine (25 mg) on Days 1, 5 and 10. On Days 1, 5, and 10, dried blood
spot specimens are collected up to 3 times daily over 1.5 h. Single oral doses of
acetazolamide (15 mg) are given on Days 2-5 and quinine (80 mg) on Days 7-10. Blood, oral
fluid, and breath specimens are collected for up to 71 h, 70 h, and 22 h, respectively, after
drug administration on Days 1, 4, 5, 9 and 10. Participants will wear the AutoSense device on
Days 1, 3, 4, 5, 8, 9 and 10 for up to 12 hours each day. All voided urine is collected
throughout the study.
Outcome measures: Primary outcome measures include cocaine, benzoylecgonine, ecgonine
methylester, norcocaine, acetazolamide, and quinine pharmacokinetics in plasma and urine and
whether subjective and cardiovascular responses to IV cocaine are changed when coadministered
with oral acetazolamide or quinine. Secondary outcome measures include cocaine
pharmacokinetics in oral fluid and breath, plasma activity of BChE and carboxylesterase
(enzymes which metabolize cocaine), and basal and post-cocaine administration serum
concentrations of leptin and other appetitive peptides (e.g. ghrelin, GLP-1, insulin, PYY,
amylin).
Benefits: There is no direct benefit to participants, but the study is likely to yield
generalizable knowledge about the feasibility of acetazolamide and quinine as markers of
medication adherence in future studies of pharmacological treatment for cocaine dependence.
Risks: <TAB>This study poses greater than minimal risk for participants because of IV cocaine
administration.
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