A Novel Compound for Alcoholism Treatment

December 13, 2019 updated by: National Institute on Alcohol Abuse and Alcoholism (NIAAA)

A Novel Compound for Alcoholism Treatment: A Translational Strategy

Background:

- Hormones are naturally occurring chemicals in your body. Ghrelin is a hormone that is mainly produced by the stomach and stimulates appetite. Some studies suggest it may stimulate alcohol craving and use. Drugs have been developed that block ghrelin. Researchers want to know if people can tolerate a particular drug that blocks ghrelin. It will be given at two dose levels, combined with alcohol.

Objective:

- To determine if a drug that may decrease alcohol consumption when given along with alcohol is safe and tolerable.

Eligibility:

  • Healthy adults 21-65 years old who have 14 (women) to 21 (men) drinks a week.
  • No one of childbearing potential can participate.

Design:

  • Participants will have 3 inpatient clinic visits; each will last 4 days.
  • They will have physical exam and blood and urine tests.
  • They will have breath tests for alcohol and smoking.
  • They will answer health and mood questions.
  • Researchers will measure their reaction to smelling alcohol and tasting a sweet drink.
  • They will eat only the food provided by the clinic. They will keep a food diary 1 day before each stay.
  • They will be randomly assigned to take the study drug or placebo 5 times each stay.
  • On Day 3, they will drink alcohol after taking the drug. They will give many blood samples that day through a tube inserted in their skin.
  • Smokers can take smoke breaks. Once, they will smoke a cigarette through a device.
  • One week after the last stay, participants will have a follow-up visit to answer questions.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Objective: Ghrelin is a 28-aminoacid peptide that stimulates appetite and food intake. It is an endogenous ligand for the growth hormone secretagogue receptor (GHSR1a). Preclinical studies suggest that ghrelin modulates alcohol reward processing. Furthermore, findings from a translational human lab study at Brown University (PI: Leggio) indicate that intravenous (IV) ghrelin administration, compared to placebo, results in an acute increase in craving for alcohol during a cue-reactivity experiment in alcoholic individuals. Therefore, an orally bioavailable, ghrelin receptor antagonist, that can pass through the blood brain barrier holds particular promise as an AD treatment. This project has been recently funded by NCATS. The goals of this protocol are to generate preliminary evidence on the safety and efficacy of a ghrelin receptor antagonist (GHSR1a antagonist), PF-05190457, an existing molecule available under the NIH-Industry Pilot Program at NCATS.

Study population: Non-treatment seeking heavy drinkers (n =20). The study will be conducted in the Inpatient Unit at the NIAAA Intramural Clinical Program.

Study Design: Single-blind dose-escalating placebo-controlled inpatient study using PF-05190457, in non-treatment seeking heavy drinking subjects. This Phase 1b study will be a within-subject design.

Outcome measures: Primary objectives will be to determine: 1) the number of adverse events (AEs) experienced, compared between all three PF-05190457 dose categories (0mg or placebo, 50mg, and 100mg b.i.d.); and 2) the total concentration of the drug, compared between the two non-placebo drug doses (50mg and 100mg b.i.d.), when co-administered with alcohol. We hypothesize that both doses of PF-05190457, as compared to placebo, will not result in an increased number of AEs. As a secondary objective, we will determine whether PF-05190457 dose-dependently affects the subjective effects of alcohol and craving. We will include pharmacokinetics (PK) and pharmacodynamic (PD) investigations conducted at University of Rhode Island (URI; Associate Investigator: Akhlaghi). The PK/PD component will include (i) measuring total, unbound or tissue concentrations of the drug using liquid chromatography tandem mass spectrometry (LC-MS/MS) and evaluation of biomarkers of effect and (ii) estimation of PK and PD parameters by the use of conventional and semi-mechanistic modeling approaches to assist in identifying an optimal dosing regimen of the drug in AD.

Study Type

Interventional

Enrollment (Actual)

14

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Maryland
      • Bethesda, Maryland, United States, 20892
        • National Institutes of Health Clinical Center, 9000 Rockville Pike

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

21 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

  • INCLUSION CRITERIA:
  • Males or females 21-65 years old (inclusive);
  • Heavy drinking defined as on average at least 21 drinks per week for men or at least 14 drinks for women based on the timeline follow-back (TLFB) done at screening.
  • Be in good health as confirmed by medical history, physical examination, ECG, blood/urine lab tests;

  • Female subjects must be of non childbearing potential as defined by at least one of the following criteria:

    • Females 45 65 years old, who are menopausal, defined as follows:

      • Females who are between 45 55 years old: they will be considered menopausal if they satisfy all the following three requirements during screening: 1) they are in amenorrhea, defined as absence of menstruation for the previous 12 months; 2) they have a negative urine pregnancy test; and 3) they have a serum FSH level within the laboratory s reference range for postmenopausal females.
      • Females who are between 56 65 years old: they will be considered menopausal if they are in amenorrhea, defined as absence of menstruation for the previous 12 months before screening.
    • OR
    • Females 21-65 years old, who have a documented hysterectomy and/or bilateral oophorectomy.
    • All other female subjects (including females with tubal ligations and females that do NOT have a documented hysterectomy) will be considered to be of childbearing potential.

  • Male subjects must use one of the following methods of contraception from the first dose of study medication and until 28 days after dosing:

    • Abstinence.

    • A condom AND one of the following:

      • Vasectomy for more than 6 months.

      • Female partner who meets one of the following conditions:

        • Has had a tubal ligation, hysterectomy, or bilateral oophorectomy;
        • Is post menopausal;

        • Uses one of the following forms of contraception:

          • Copper or hormonal containing IUD;
          • Spermicidal foam/gel/film/cream/suppository;
          • Diaphragm with spermicide;
          • Oral contraceptive;
          • Injectable progesterone;
          • Subdermal implant.

EXCLUSION CRITERIA:

  • Interest in receiving treatment for heavy drinking.
  • Current DSM-IV diagnosis (based on SCID) of substance dependence (other than alcohol and/or nicotine); a negative urine drug screen will also be required.
  • DSM-IV Axis I criteria for a lifetime diagnosis of schizophrenia, bipolar disorder, or other psychoses;
  • Active illness within the past 6 months of the screening visit that meet the DSM-IV criteria for a diagnosis of major depressive disorder or anxiety disorder; subjects with a history of attempted suicide will be excluded;
  • Clinically significant medical abnormalities (e.g., unstable hypertension, clinically significant EKG abnormalities, Creatinine greater than or equal to 2 mg/dL, liver cirrhosis, AST or ALT > 3x the upper normal limit, hemoglobin <10.5 g/dl);
  • Heart rate >100 at screening on two separate measurements given potential of study medication to increase heart rate.
  • BMI less than or equal to 18.5 or anorexia given potential of the study medication to reduce appetite.
  • BMI greater than or equal to 35 kg/m^2.

  • Exclusionary Medications:

    • Naltrexone, acamprosate, alcohol dehydrogenase inhibitors, topiramate, gabapentin, ondansetron, benzodiazepines, beta-blockers, H2-blockers, and alpha-1 blockers, baclofen, and barbiturates as well as hormone replacement therapy; medications and dietary/herbal supplements (like St. John's wort) that interact with Cytochrome P450 3A4. All of the medications in the previous sentence will not be allowed if they have been taken within 2 weeks of study medication administration.
    • PF-05190457 is a substrate for P-glycoproteins (P-gp or encoded by ABCB1 gene) based on information from in vitro or animal models. Patients that are required to take the following inhibitors and inducers of P-gp are excluded unless the subject stops taking these agents for 2 weeks for P-gp inhibitors or 6 weeks for P-gp inducers before study medication administration.

Inhibitors: Amiodarone, azithromycin, captopril, carvedilol, clarithromycin, conivaptan, cyclosporine, diltiazem, dronedarone, erythromycin, felodipine, itraconazole, ketoconazole, lopinavir and ritonavir, quercetin, quinidine, ranolazine, verapamil

Inducers: Avasimibe, carbamazepine, phenytoin, rifampin, St John s wort, tipranavir/ritonavir [From Drug Development and Drug Interactions: Table of Substrates, Inhibitors and Inducers, table 12, from http://www.fda.gov/Drugs/DevelopmentApprovalProcess/DevelopmentResources/DrugInteractionsLabeling/ucm093664.htm#substrates]

  • History of epilepsy or alcohol-related seizures;
  • patients who have diabetes and/or are treated with any drug with glucose lowering properties such as sulfonylurea, insulin, metformin, thiazolidinediones (TZD), Dipeptidyl peptidase-4(DPP4) inhibitors, or Glucagon-like peptide-1(GLP-1)agonists (due to the glucose-lowering properties of PF-05190457 observed in healthy volunteers);
  • History of alcohol-induced flushing reactions.
  • Clinically significant alcohol withdrawal symptoms, as assessed by a CIWA-Ar score > 8 at screening.
  • Any other reason or clinical condition for which the PI or the MAI will consider unsafe for a possible participant to participate in this study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Side effects/adverse events and maximum tolerated dose of PF-05190457 alone and in combination with alcohol administration.
Time Frame: 3 days
3 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Collaborators

National Center for Advancing Translational Sciences (NCATS)
University of Rhode Island

Investigators

  • Principal Investigator: Lorenzo Leggio, M.D., National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 3, 2014

Primary Completion (Actual)

October 1, 2015

Study Completion (Actual)

December 24, 2017

Study Registration Dates

First Submitted

January 15, 2014

First Submitted That Met QC Criteria

January 15, 2014

First Posted (Estimate)

January 17, 2014

Study Record Updates

Last Update Posted (Actual)

December 16, 2019

Last Update Submitted That Met QC Criteria

December 13, 2019

Last Verified

December 24, 2017

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 140042
  • 14-AA-0042

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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