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Continuous Methamphetamine DependencePhase 1NCT02014064

Safety Study to Assess Atomoxetine With MA Abusers and Healthy Controls

A Phase 1 study testing Atomoxetine in people with Continuous Methamphetamine Dependence and Methamphetamine Dependence in Remission, run by University of California, Los Angeles.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

Methamphetamine (MA) abuse is a national public health concern. People who are dependent on MA have problems with mental functions (e.g., learning, remembering, focusing attention, solving problems). Such problems can interfere with their treatment for MA abuse, and thereby may promote continued drug use. Read more about this study

Who is it for?
Ages 18 to 50 yearsHealthy volunteers can take part
What is being tested?
Atomoxetine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
41 participants
Where
No sites listed yet
Study dates
Aug 2009to Aug 2012
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 50 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • -
  • MA ABUSING PARTICIPANTS:
  • In order to participate in the study, MA-using subjects must:
  • Be fluently English-speaking volunteers who meet DSM-IV criteria for MA abuse or dependence.
  • Be between 18 and 50 years of age.
  • Be able to verbalize understanding of consent form, able to provide written informed consent, and verbalize willingness to complete study procedures.
Show all 33Show fewer
  • Have smoked or injected methamphetamine for more than two years.
  • Produce a methamphetamine-positive urine prior to study entry.
  • Have vital signs as follows: resting pulse between 50 and 90 bpm, blood pressures between 105-150mm Hg systolic and 45-90mm Hg diastolic. Note: MA Abusing participants may present with elevated vital signs during the intake screening phase as a result of MA intoxication or anxiety and elevated vital signs may occur after inclusion to the study prior to administration or Methamphetamine or study compound. Participants must have vital signs within the aforementioned range on two timepoints (i.e., morning or night vital collection) during two consecutive days prior to randomization or participation will be terminated.
  • Have an ECG performed that demonstrates normal sinus rhythm, normal conduction, and no clinically significant arrhythmias.
  • Agree to abstain from MA during the study, evidenced by a MA-negative urine each morning of the study.
  • If female, have a negative pregnancy test and agree to use one of the following methods of birth control, or be postmenopausal, have had a hysterectomy or have been sterilized.
  • oral contraceptives
  • barrier (diaphragm or condom) with spermicide, or condom only
  • intrauterine progesterone, or non-hormonal contraceptive system
  • levonorgestrel implant
  • medroxyprogesterone acetate contraceptive injection
  • complete abstinence from sexual intercourse NOTE: Recent intermittent alcohol or other illicit drug use without physical dependence is allowable (however a benzodiazepine-free urine should be produced to document absence of recent use).
  • HEALTHY CONTROL PARTICIPANTS
  • In order to participate in the study, normal control subjects must:
  • Be fluently English-speaking volunteers.
  • Be between 18 and 50 years of age.
  • Be able to verbalize understanding of consent form, able to provide written informed consent, and verbalize willingness to complete study procedures.
  • Have vital signs as follows during two visits prior to medication administration: resting pulse between 50 and 90 bpm, blood pressures between 105-150mm Hg systolic and 45-90mm Hg diastolic. Note that a blood pressure of 150/90 and pulse of 90 is too high for randomization but will allow participants to be enrolled if an acceptable range is demonstrated on a two separate occasions prior to atomoxetine compound administration.
  • Have an ECG performed that demonstrates normal sinus rhythm, normal conduction, and no clinically significant arrhythmias.
  • Agree to abstain from any and all substances of abuse during the study, evidenced by toxicology-negative urine each day prior to study procedures.
  • If female, have a negative pregnancy test and agree to use one of the following methods of birth control, or be postmenopausal, have had a hysterectomy or have been sterilized.
  • oral contraceptives
  • barrier (diaphragm or condom) with spermicide, or condom only
  • intrauterine progesterone,or non-hormonal contraceptive system
  • levonorgestrel implant
  • medroxyprogesterone acetate contraceptive injection
  • complete abstinence from sexual intercourse

Who cannot join

  • MA ABUSING PARTICIPANTS:
  • A current or past history of seizure disorder, including alcohol- or stimulant-related seizure, febrile seizure, or significant family history of idiopathic seizure disorder.
  • A history of head trauma that resulted in neurological sequelae (e.g., with loss of consciousness [LOC] > 15 minutes, or that required hospitalization. Also, individuals with 3 or more head injuries with LOC > 5 minutes will be excluded).
  • Meet DSM-IV criteria (by SCID) for drug dependence other than meth, with the exception of nicotine and/or marajuna dependence.
  • Any previous medically serious adverse reaction to MA including loss of consciousness, chest pain, or epileptic seizure resulting in hospitalization.
  • Meeting diagnostic criteria or receiving psychopharmacological treatment for the following Axis I disorders within the last 6 months: anorexia nervosa, bulimia, psychosis, bipolar I disorder, organic brain disease, dementia, major depression, schizoaffective disorder, or schizophrenia.
Show all 71Show fewer
  • Evidence of clinically significant heart disease, hypertension or significant medical illness.
  • Have any history of hypersensitivity to atomoxetine, glaucoma, motor tics or with a family history or diagnosis of Tourette's syndrome.
  • Have any preexisting severe gastrointestinal narrowing, small bowel inflammatory disease, intestinal adhesions, past history of peritonitis, or cystic fibrosis.
  • Be pregnant or nursing.
  • Have a significant family history of early cardiovascular morbidity or mortality.
  • Have a diagnosis of adult asthma, including those with a history of acute asthma within the past two years, and those with current or recent (past 2 years) treatment with inhaled or oral beta-agonist or steroid therapy (due to potential serious adverse interactions with methamphetamine).
  • Be actively using albuterol or other beta agonist medications, regardless of formal diagnosis of asthma.
  • (Inhalers are sometimes used by MA addicts to enhance MA delivery to the lungs.) If respiratory disease is excluded and the subject will consent to discontinue agonist use, s/he may be considered for inclusion.
  • For subjects suspect for asthma but without formal diagnosis, 1) have a history of coughing and/or wheezing, 2) have a history of asthma and/or asthma treatment two or more years before, 3) have a history of other respiratory illness, e.g., complications of pulmonary disease (exclude if on beta agonists), 4) use over-the-counter agonist or allergy medication for respiratory problems (e.g., Primatene Mist): a detailed history and physical exam, pulmonary consult, and pulmonary function tests should be performed prior to including or excluding from the study or 5) have an FEV1 <70 %.
  • Have any illness, condition, and/or use of medications that in the opinion of the site Principal Investigator and the admitting physician would preclude safe and/or successful completion of the study.
  • Have active syphilis that has not been treated or refuse treatment for syphilis.
  • Be undergoing HIV treatment with antiviral and non-antiviral therapy (participants who are HIV positive may not be eligible for cognitive assessments or brain scans and may only participate in the safety aspect of the protocol.)
  • Have AIDS according to the current CDC criteria for AIDS - MMWR 1999;48 (#RR-13:29-31).
  • Have neurological disorders including Parkinson's disease.
  • Have evidence of significant liver or kidney dysfunction.
  • Have a history of urinary retention or bladder outlet obstruction.
  • Be UCLA students or staff.
  • Have evidence of active tuberculosis infection.
  • Only for MRI Procedures:
  • We will exclude any participant from participanting in MRI scans whose body contains a ferromagnetic implanted device that might produce a safety hazard during fMRI. We will follow guidelines found in the manual, Magnetic Resonance: Bioeffects, Safety, and Patient Management72 ,supplemented by the current information published on the International MR Safety Web Site: http://www.mrisafety.com/safety_info.asp Criteria for Discontinuation Following Initiation
  • 1. Positive urine drug screen or breath test indicating illicit use of cocaine, MA, alcohol, opiates, or other abused drugs not delivered as part of this protocol; 2. Inability to comply with study procedures; 3. Meet discontinuation criteria due to exaggerated response to MA, described below.
  • Stopping Criteria Participants must continue to meet inclusion criteria in order to remain in the protocol. Thus, MA administration procedures will not be initiated if there are clinically significant arrhythmias or if vital signs are outside of acceptable ranges: Resting Pulse: 50-90 beats per minute. Systolic Blood Pressure: 105-140 mm Hg Diastolic Blood Pressure: 45-90 mm Hg In addition, repeated doses of MA will not be administered (and the study physician or nurse practitioner will halt continued MA delivery) if there are behavioral manifestations of MA toxicity (agitation, psychosis, inability to cooperate with study procedures). Note that participants remain eligible to remain in the study provided that vital signs do not exceed the limits below.
  • Stopping Criteria for Further Participation
  • Subject participation will be terminated if any of the following events occur:
  • Systolic BP > 200 mm Hg sustained;
  • Diastolic BP > 110 mm Hg sustained;
  • Heart rate > (220 - age) x 0.85 bpm.
  • A clinically significant ECG abnormality, such as:
  • ST segment elevations in two or more continuous ads of greater than 0.1 mV.
  • ST segment depression of greater than 1 mm that are flat or down-sloping at 80 msec after the J point.
  • New bundle branch block.
  • Mobitz II 20 or 30 heart block.
  • Atrial fibrillation or atrial flutter or activation of any tachyarrhythmia for greater than 10 sec.
  • QTc >440 msec for males and >450 msec for females.
  • An uncorrected QT of 470 msec or a rate-corrected QTc of 500 msec or greater is observed and does not revert to baseline within 10 min.
  • Three or more consecutive ectopic ventricular complexes at a rate of greater than 100/min.
  • These are extreme values and we do not anticipate this would occur based on prior experience by ours and other groups administering repeated doses of MA in the laboratory.
  • HEALTHY CONTROL PARTICIPANTS
  • Have a current or past history of seizure disorder, including alcohol- or stimulant-related seizure, febrile seizure, or significant family history of idiopathic seizure disorder.
  • A history of head trauma that resulted in neurological sequelae (e.g., with loss of consciousness [LOC] > 15 minutes, or that required hospitalization. Also, individuals with 3 or more head injuries with LOC > 5 minutes will be excluded).
  • Meet criteria for abuse or dependence of either alcohol or other illicit substances (other than nicotine).
  • Have physiological dependence on alcohol or a sedative-hypnotic, (e.g., a benzodiazepine) that requires medical detoxification.
  • Meet the diagnostic criteria for the following Axis I disorders: psychosis, bipolar I disorder, organic brain disease, dementia, major depression, schizoaffective disorder, or schizophrenia.
  • Have any evidence of clinically significant heart disease, hypertension or significant medical illness.
  • Have any history of hypersensitivity to atomoxetine, glaucoma, motor tics or with a family history or diagnosis of Tourette's syndrome.
  • Have any preexisting severe gastrointestinal narrowing, small bowel inflammatory disease, intestinal adhesions, past history of peritonitis, or cystic fibrosis.
  • Be pregnant or nursing.
  • Have a significant family history of early cardiovascular morbidity or mortality.
  • Have a diagnosis of adult asthma, including those with a history of acute asthma within the past two years, and those with current or recent (past 2 years) treatment with inhaled or oral beta-agonist or steroid therapy (due to potential serious adverse interactions with atomoxetine).
  • Be actively using albuterol or other beta agonist medications, regardless of formal diagnosis of asthma. If respiratory disease is excluded and the subject will consent to discontinue agonist use, s/he may be considered for inclusion.
  • For subjects suspect for asthma but without formal diagnosis, 1) have a history of coughing and/or wheezing, 2) have a history of asthma and/or asthma treatment two or more years before, 3) have a history of other respiratory illness, e.g., complications of pulmonary disease (exclude if on beta agonists), 4) use over-the-counter agonist or allergy medication for respiratory problems (e.g., Primatene Mist): a detailed history and physical exam, pulmonary consult, and pulmonary function tests should be performed prior to including or excluding from the study or 5) have an FEV1 <70 %.
  • Have any illness, condition, and/or use of medications that in the opinion of the site Principal Investigator and the admitting physician would preclude safe and/or successful completion of the study.
  • Have active syphilis that has not been treated or refuse treatment for syphilis (see note).
  • Subjects who are HIV-positive will be excluded because HIV infection and the development of AIDS produce alterations in brain activity. Such effects on brain activity could confound the results of this study.
  • Have a current or past history of anorexia nervosa or bulimia disorder.
  • Have neurological disorders including Parkinson's disease.
  • Have evidence of significant liver or kidney dysfunction.
  • Have a history of urinary retention or bladder outlet obstruction.
  • Be UCLA students or staff.
  • Have evidence of active tuberculosis infection.
  • Only for MRI Procedures:
  • We will exclude any participant from MRI scanning procedures whose body contains a ferromagnetic implanted device that might produce a safety hazard during fMRI. We will follow guidelines found in the manual, Magnetic Resonance: Bioeffects, Safety, and Patient Management72 ,supplemented by the current information published on the International MR Safety Web Site: http://www.mrisafety.com/safety_info.asp Note: Syphilis testing will not be performed as part of this study and the study will rely solely on subjects' self report.
  • Criteria for Discontinuation Following Initiation
  • Positive urine drug screen or breath test indicating illicit use of cocaine, MA, alcohol, opiates, or other abused drugs not delivered as part of this protocol;
  • Inability to comply with study procedures. -

About this study

Official title: A Study to Assess the Cardiovascular, Cognitive and Subjective Effects of Atomoxetine in Combination With Intravenous Methamphetamine

Methamphetamine (MA) abuse is a national public health concern. People who are dependent on MA have problems with mental functions (e.g., learning, remembering, focusing attention, solving problems). Such problems can interfere with their treatment for MA abuse, and thereby may promote continued drug use. While the effects of MA have been studied in rodents and non-human primates, its effects on the human brain have not been well characterized.

This is a study of nontreatment seeking individuals who use MA compared to individuals who do not use MA(control participants). The study has three goals: 1. it aims to identify the brain regions and pathways that may contribute to the problems of MA abusers in performing mental tasks; 2. it will serve as a double-blind, placebocontrolled,within-subjects study to determine the safety and tolerability, and positive effects of MA in MA-abusing volunteers treated with atomoxetine or placebo; 3. It aims to compare the brain activity as measured by structuraland functional magnetic resonance imaging (fMRI). These are noninvasive brain imaging procedures, that will be used to study brain function while control and MA using participants take atomoxetine or placebo and perform tests of memory and concentration.

Read more

MA abusing participants will undergo a 1-day outpatient screening and if it is safe for the participants to proceed with the study they will participate in two inpatient phases of the study that will occur in the UCLA research setting, the General Clinical Research Center. The first inpatient stay will be 15 days, and the second will be a 9 days stay that includes drug administration and assessments. There will be at least a two week interval between inpatient phases. During the inpatient phases participants will receive alternating study drugs; atomoxetine or placebo and four sessions of IV MA administration or placebo.

The study schedule for control participants will include a 1-day outpatient screening and two phases of outpatient administration of atomoxotime or placebo with a two week study drug free interval between the phases. Four to five of the outpatient study visits will involve cognitive tests and brain imaging studies.

Read the detailed description

As a preliminary step, the investigators will screen the experimental data for normality and for potential associations between outcome variables with demographic variables at baseline. In cases of strong deviations from normality, log or power transformations will be used as appropriate. For the subjective effects questionnaires, the peak effect will be identified for each subject and used as the dependent variable. The primary analytical technique will be linear mixed effects regression. The general linear mixed model (GLMM) is equivalent to repeated measures ANOVA when all subjects have complete data but automatically handles missing observations, producing unbiased estimates as long as the values are missing at random. This approach will allow use of the data from subjects who complete only part of the protocol or who have invalid measurements on some tests, greatly enhancing our power.

The sample size is as large or greater than those in the previous human laboratory studies assessing safety and initial efficacy of agonist-like pharmacotherapies for stimulant dependence. For example, these previous studies used samples of 7 (Herin et al., 2010; Stoops et al., 2008; Dackis et al., 2003), and 10 (Sofuoglu et al., 2009) subjects to obtain significant reductions in subjective effects of d-amphetamine by atomoxetine and those of cocaine by modafinil.

To be conservative, the investigators base power estimates on completers but will use available data from all 30 subjects in GLMM analyses. This should substantially increase power (power for GLMM and repeated measures ANOVA are equivalent except that ANOVA cannot utilize incomplete data, while a GLMM can).

Being tested
Atomoxetine, Placebo
Keywords
Methamphetamine, Atomoxetine, Clinical Pharmacology

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • AtomoxetineDrug

    Also called Strattera

    MA Group: Dispense 1 cap @ 8 AM on Treatment day 9 and 10 (total daily dose 40mg or 0); 1 cap SID @ 8 AM and 4 PM on day 11,12, and 13 (total daily dose 80mg or 0); 1 cap @ 8 AM on day 14 (total daily dose, 40mg or 0).

    Control Group Schedule:

    • Day 1: 40mg @ 8:00am
    • Day 2: 40mg @ 8:00am
    • Day 3: 40mg @ 8:00am, 40mg @ 8:00pm
    • Day 4: 40mg @ 8:00am, 40mg @ 8:00pm
    • Day 5: 40mg @ 8:00am, 40mg @ 8:00pm
    • Day 6: 40mg @ 8:00am = Testing day (fMRI scan \& cognitive testing session)

  • PlaceboOther

    Control Group: Day 1: 40mg @ 8am Day 2: 40mg @ 8am Day 3: 40mg @ 8am, 40mg @ 8pm Day 4: 40 mg @ 8am, 40mg @ 8pm Day 5: 40mg @ 8am, 40 mg @ 8pm Day 6: 40 mg @ 8am = Testing day (fMRI scan \& cognitive testing session)

Study groups in NCT02014064
Study groupRoleWhat they receive
AtomoxetineExperimentalDouble-blind, Placebo controlled, 2-phase study the safety \& efficacy of Atomoxetine
Receives: Drug: Atomoxetine
PlaceboPlacebo comparatorControl Group Schedule: Day 1: 40mg @ 8:00am Day 2: 40mg @ 8:00am Day 3: 40mg @ 8:00am, 40mg @ 8:00pm Day 4: 40mg @ 8:00am, 40mg @ 8:00pm Day 5: 40mg @ 8:00am, 40mg @ 8:00pm Day 6: 40mg @ 8:00am = Testing day (fMRI scan \& cognitive testing session)
Receives: Other: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Cardiovascular & Subjective Effects of Methamphetamine & Atomoxetine

    Participants will be followed for the duration of the study, an expected average of 4 weeks

    Measured: 4 weeks

Secondary outcomes (3)

  1. The effects of administration of atomoxetine on the preference of MA-using subjects for MA (0 and 15mg, IV) versus escalating doses of money, from $0.25 to $64 in a Multiple-Choice Procedure.

    Participants will be followed for the duration of study, an expected average of 4 weeks

    Measured: 4 weeks

  2. The effects of atomoxetine administration on cognitive function, as determined by measures of performance on cognitive tests, such as working memory tasks and reaction time tests

    Participants will be followed for the duration of study, an expected average of 4 weeks

    Measured: 4 weeks

  3. The effects of administration of atomoxetine on BOLD fMRI signals in the brain in MA users and normal controls.

    Participants will be followed for the duration of study, an expected average of 4 weeks

    Measured: 4 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Dec 2013 (estimated)
  2. Study startAug 2009
  3. Primary completionAug 2012
  4. Study completionAug 2012

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
41 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02014064
Sponsor's protocol ID
NCT02014064
Status last verified
May 2016
First submitted
5 Aug 2011
Last updated
12 May 2016
Results posted
No
Data monitoring committee
Yes
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing Atomoxetine in people with Continuous Methamphetamine Dependence and Methamphetamine Dependence in Remission, run by University of California, Los Angeles.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 33 inclusion and 71 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 May 2016. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Cardiovascular & Subjective Effects of Methamphetamine & Atomoxetine (time frame: 4 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02014064.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 May 2016.

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