grant

The potential therapeutic effects of N, N-dimethyltryptamine (DMT) on alcohol use disorder (AUD)

Organization YALE UNIVERSITYLocation NEW HAVEN, UNITED STATESPosted 15 Aug 2023Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY20245-HT-2A Gene5-HT2A5-Hydroxytryptamine (Serotonin) Receptor 2A Gene5-Hydroxytryptamine Receptor 2A5-Hydroxytryptamine Receptor 2A GeneAbsolute ethanolAbstinenceActive Follow-upAcuteAdverse ExperienceAdverse eventAlcohol Chemical ClassAlcohol DrinkingAlcohol consumptionAlcoholsAnimalsAnxietyAttentionAyahuascaBackBanisteriopsisBenadrylBendylateBenhydraminBenzhydramineBindingBrief PsychotherapyCause of DeathClinicalClinical TrialsConsumptionCross-Product RatioDSM-5DSM-VDSM5DevelopmentDiagnosisDiagnostic and Statistical Manual of Mental Disorders, 5th editionDiagnostic and Statistical Manual of Mental Disorders-VDimethyltryptamineDiphenhydramineDiphenylhydraminDiphenylhydramineDorsumDoseDouble-Blind MethodDouble-Blind StudyDouble-BlindedDouble-Masked MethodDouble-Masked StudyDrugsETOHETOH levelEldadrylEmotional DepressionEtOH drinkingEtOH useEthanolEthyl AlcoholFDA approvedGrain AlcoholHTR2HTR2 GeneHTR2AHTR2A geneHallucinogenic AgentsHallucinogenic DrugsHallucinogenic SubstancesHallucinogensHeavy DrinkingHospitalsHourHumanIndigenousIndividualInterviewIntravenousLSD-25LaboratoriesLaboratory StudyLiteratureLong-Term EffectsLongterm EffectsLysergic Acid DiethylamideLysergideMeasuresMedicalMedicationMedicineMental DepressionMental disordersMental health disordersMeta-AnalysisMethodologyMethodsMethylcarbinolMiceMice MammalsModern ManMolecular InteractionMonitorMurineMusN,N-DimethyltryptamineN,N-dimethyl-1H-indole-3-ethanamineObservation researchObservation studyObservational StudyObservational researchOdds RatioOral AdministrationOral Drug AdministrationOut-patientsOutcomeOutpatientsParticipantPatient Self-ReportPharmaceutical PreparationsPharmacological TreatmentPhasePlacebo ControlPlacebosPsilocibinPsilocybinPsychedelic AgentsPsychedelicsPsychiatric DiseasePsychiatric DisorderPsychotherapyPsychotomimetic AgentsQuestionnairesRandomizedRandomized Controlled Clinical TrialsRelative OddsReportingRiskRisk RatioSafetySample SizeSelf AdministeredSelf AdministrationSelf-ReportSerotonin 5-HT-2 Receptor GeneSerotonin 5-HT-2A ReceptorSham TreatmentShort-Term PsychotherapySouth AmericanSubstance Use DisorderTeaTherapeuticTherapeutic EffectTribesUnited StatesVisualWomanactive followupalcohol abuse therapyalcohol abuse treatmentalcohol ingestionalcohol intakealcohol levelalcohol measurementalcohol product usealcohol treatmentalcohol usealcohol use disorderalcoholic beverage consumptionalcoholic drink intakeanaloganxiety reductionanxiety symptomsanxious symptombehavioral sensitizationcompare to controlcomparison controlconditioned place preferenceconsumption measuresdepressiondepression symptomdepressivedepressive symptomsdetermine efficacydevelopmentaldrink heavilydrinkingdrug/agentefficacy analysisefficacy assessmentefficacy determinationefficacy evaluationefficacy examinationethanol consumptionethanol drinkingethanol ingestionethanol intakeethanol measurementethanol product useethanol useethanol use disorderethyl alcohol measurementsevaluate efficacyexamine efficacyexcessive alcohol consumptionexcessive alcohol ingestionexcessive alcohol intakeexcessive drinkingexcessive ethanol ingestionexperienceextreme drinkingfollow upfollow-upfollowed upfollowupheavy alcohol useimprovedinterestintraoral drug deliveryintravenous administrationmenmental illnessmotivational enhancement therapymotivational interviewnovelplace conditioningplacebo controlledpre-clinical studypreclinical studyprimary outcomepsychedelic drugpsychiatric illnesspsychoeducationpsychological disorderpsychotomimetic drugrandomisationrandomizationrandomized control clinical trialrandomly assignedsham therapysubstance use and disordertimeline
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Full Description

ABSTRACT
There is an urgent need to develop novel pharmacological treatment for alcohol use disorder (AUD). Recently,

psychedelic compounds have attracted great attention in treatment of different psychiatric disorders following

their reported fast-acting and long-lasting effects. Preliminary evidence from observational studies, supported

by animal studies, is promising for the potential therapeutic effects of psychedelic N,N-dimethyltryptamine

(DMT) for AUD. Here, we propose to investigate the therapeutic potential of a single dose of intravenous DMT

plus a brief course of psychotherapy (including Motivational Enhancement Therapy (MET)) on alcohol

consumption in non-treatment seeking individuals with AUD, in a proof-of-concept, randomized (1:1), placebo-

controlled, double-blind, parallel group, laboratory study and clinical trial.

Methods: Otherwise healthy individuals with diagnosis of moderate to severe AUD (based on DSM5) will be

randomized to receive a single dose of intravenous DMT or active placebo (diphenhydramine). Vitals will be

closely monitored, tolerability will be measured using a Visual Analogue Scale (VAS), and DMT acute

psychedelic effects will be assessed using the Mystical Experience Questionnaire (MEQ), at the end of the

dosing day. Adverse events will be assessed using the Systematic Assessment for Treatment Emergent

Effects (SAFTEE) interview on the dosing day and weekly follow up sessions (4 weeks). One day following

drug administration, participants will attend an experimental session using Alcohol Drinking Paradigm (ADP).

All participants will consume a priming dose of alcohol at the beginning of the experimental session, which will

be followed by two 1-hour self-administration drinking sessions, over which participants will have a choice of

consuming a total of 8 drinks or receiving $5 for each drink that is not consumed. The total number of

consumed drinks is the main primary outcome. All participants will receive a brief course of psychotherapy

(including MET). We will explore the effects of DMT (plus brief psychotherapy) on participants' natural alcohol

consumption weekly for 4 weeks, using Timeline follow-back (TLFB), to measure the percentage of heavy

drinking days, abstinent days, and total amount of alcohol consumption and categorical outcomes of

abstinence, no heavy drinking and a 2-level reduction in WHO drinking risk will be compared.

Hypotheses: Relative to control (diphenhydramine, IV, 25 mg plus MET), a single psychedelic dose of

intravenous (IV) DMT (0.3 mg/kg) plus brief psychotherapy (including MET) in individuals with AUD will 1) be

safe and well-tolerated, 2) reduce alcohol consumption measured in the laboratory using Alcohol Drinking

Paradigm, the day after, and 3) reduce alcohol drinking over the following 4 weeks.

Grant Number: 5R21AA030649-02
NIH Institute/Center: NIH

Principal Investigator: Anahita Bassir Nia

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