Definition of alcoholism dsm 5. A Novel Compound for Alcoholism Treatment - Full Text View -

- 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. Clinical definition of alcoholism.

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

Healthy adults 21 65 years old who have 14 (women) to 21 (men) drinks a week.

No one of childbearing potential can participate.

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.

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.

Definition of alcoholism uk

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.

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.

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:

A condom AND one of the following:

Definition of alcoholic fermentation

Vasectomy for more than 6 months.

Female partner who meets one of the following conditions:

Has had a tubal ligation, hysterectomy, or bilateral oophorectomy,

Uses one of the following forms of contraception:

Copper or hormonal containing IUD,

Spermicidal foam/gel/film/cream/suppository,

Diaphragm with spermicide,

Injectable progesterone,

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.

Clinical definition of binge drinking

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]

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.

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