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Completed

NCT Number: NCT02262026

The Tolerability and Effects of AZD0530 in Individuals With or Without a Family History of Alcoholism

Functional neuroimaging of alcoholism vulnerability: glutamate, reward, impulsivity, and Pavlovian-to-instrumental transfer (PIT), part II Saracatinib

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Hartford Hospital

Hartford, Connecticut, 06102, United States

About this study

To assess the effect of oral AZ D0530 at various doses on neuroimaging parameters associated with various forms of impulsivity mediated through glutamate-dopamine interactions, as ascertained through functional magnetic resonance imaging. -- --NOTE-- AZD0530 dosage of 50mg was discontinued by manufacturer. Adjustments were made to account for the removal of the 50mg dosage in all arms of the study.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clear History of a father having a history of alcoholism, OR a mother AND another 1st or 2nd degree relative having a history of alcoholism, OR no 1st or 2nd degree relatives with alcoholism or substance abuse

Exclusion criteria

  • Current diagnosis of DSM-IV-TR Axis I disorder, or past diagnosis of any substance use disorder or moderate alcohol use disorder
  • Report of psychotic disorder in a 1º relative
  • Auditory or visual impairment that interferes with test taking
  • History of prenatal exposure to alcohol plus currently meeting criteria for features of fetal alcohol syndrome
  • Not speaking English fluently or being a non-native English speaker, or being educated in a primary language other than English >grade 1
  • Mental retardation (Full Scale IQ<70) using 2 WASI subtests for IQ estimate
  • Traumatic brain injury with loss of consciousness > 30 minutes, or concussion in last 30 days
  • Presence or history of any medical/neurologic illness that may affect brain physiology (e.g., epilepsy, Multiple Sclerosis), including focal brain lesion seen on structural MRI (all structural scans are read by a licensed radiologist)
  • Current pregnancy (all females will be tested with urine screens on the day of MRI and prior to each phase of drug treatment)
  • Positive urine screen for the presence of marijuana, cocaine, opiates or breath screen to detect the presence of alcohol, administered at each lab visit.
  • Inability to comprehend the consent form appropriately
  • Ferromagnetic metal devices, clips or fragments in body (orbital x-ray performed if needed).
  • Current use (within 30 days of screening) of specific psychoactive medications (e.g., typical neuroleptics, narcotic analgesics, antiparkinsonian medications, systemic corticosteroids, or medications with significant central anticholinergic activity, etc.). Current use of warfarin.
  • Current use of the following medications (CYP3A4 substrates whose metabolism may be slowed by AZD0530): carbamazepine, colchicine, cyclosporine, disopyramide, fluticasone, quinidine, vinblastine, vincristine, nifedipine. Patients taking sildenafil, tadalafil, and vardenafil will be advised to stop taking these medications for the duration of the trial. Patients cannot take the following drugs which inhibit the CYP3A4 isoenzyme: cimetidine, cyclosporine, danazol, fluconazole, grapefruit juice, HIV protease inhibitors, itraconazole, ketoconazole, macrolides, miconazole, nefazodone, omeprazole, ritonavir, and verapamil, aromatase inhibitors, docetaxel
  • Neutropenia defined as absolute neutrophils count of <1,500/microliter.
  • Thrombocytopenia defined as platelet count <100x103/microliter.
  • AST, ALT, total bilirubin >1.5 times upper normal; serum creatinine, >2 time upper normal limit, total bilirubin>1.5 times ULN; Serum creatinine >2.0 times ULN.
  • History of interstitial lung disease.

Treatment and study plan

125 mg AZD0530

Drug

Randomized to receive 125 mg of AZD0530

Other names: saracatinib, AZD0530

50 mg AZD0530

Drug

Randomized to receive 50 mg of AZD0530

Other names: saracatinib, AZD0530

Placebo

Drug

Placebo

Primary outcomes

  1. BOLD activation during A1 phase

    Time frame: 4 Hours post medication administration

    BOLD activation during the A1 phase of the MRI Monetary Incentive Delay task

Secondary outcomes

  1. BOLD signal activation in the anterior cingulate cortex(ACC)

    Time frame: 4 Hours post medication administration

    BOLD signal activation in the anterior cingulate cortex (ACC) observed during False Alarms of the GoNoGo Task

Sponsors and collaborators

Lead sponsor

Yale University

Other

Registry information

Official study title

A Phase One Study Investigating the Tolerability and Effects of AZD0530 on Functional Neuroimaging Responses in Individuals With or Without a Family History of Alcoholism

Important dates

Study start
2014
Primary completion
2019
Study completion
2019
First posted
Oct 10, 2014
Registry last updated
Feb 24, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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