- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07636356
THCV Treatment for Smokers
2 giugno 2026 aggiornato da: Lara Ray, PhD, University of California, Los Angeles
Development of Tetrahydrocannabivarin as a Treatment for Smokers
This study will randomize 32 non-treatment-seeking individuals who smoke cigarettes daily into a randomized, crossover, double-blind, placebo-controlled study testing the safety, tolerability, and initial efficacy of Δ9-tetrahydrocannabivarin (Δ9-THCV).
Panoramica dello studio
Stato
Non ancora reclutamento
Condizioni
Intervento / Trattamento
Descrizione dettagliata
The objective of this study is to examine the safety, tolerability, and initial efficacy of Δ9-tetrahydrocannabivarin (Δ9-THCV) in daily smokers.
We will randomize 32 non-treatment-seeking adults who smoke cigarettes daily (50% female) into a randomized, double-blind, placebo-controlled, counter-balanced, within-subject human laboratory study of Δ9-THCV (10 mg oral) and matched placebo.
Specifically, participants will complete two 5-day outpatient medication periods, with a 14-day washout period in between, during which they will receive either Δ9-THCV or placebo in a counter-balanced order, such that all participants will complete both medication conditions across the study.
Following each 5-day medication period, participants will complete a laboratory study visit during which they will undergo the McKee Smoking Lapse Task to assess the ability to resist smoking, cigarette self-administration, craving, withdrawal, and subjective effects of nicotine.
Total study participation will be approximately 4 weeks.
Tipo di studio
Interventistico
Iscrizione (Stimato)
32
Fase
- Fase 2
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Contatto studio
- Nome: Jessica Jenkins, MS
- Numero di telefono: 310-206-6756
- Email: jenkinsj@ucla.edu
Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Descrizione
Inclusion Criteria:
- Be between the ages of 21 and 65;
- Smoke 10 or more combustible cigarettes per day;
- Have fewer than 3 months of smoking abstinence in the past year;
- Has self-reported ≥10 lifetime uses of cannabis products;
- Have self-reported recent (past 3-month) use of cannabis products;
- Agree to abstain from all other cannabinoid use during the study;
- Agree to abstain from all other medication use during the study, other than methods of birth control as listed in inclusion criteria for female participants;
- Agree to one of the following methods of birth control (if female), unless she or partner are surgically sterile: oral contraceptives, Contraceptive sponge, patch, double barrier, intrauterine contraceptive device, etonogestrel implant, medroxyprogesterone acetate contraceptive injection, hormonal vaginal contraceptive ring, complete abstinence from sexual intercourse.
Exclusion Criteria:
- Have current (last 12 months) DSM-5 diagnosis of substance use disorder for any psychoactive substances other than nicotine;
- Have a lifetime DSM-5 diagnosis of schizophrenia, bipolar disorder, or any other psychotic disorder;
- Have a score of 3 or greater on the Columbia Suicide Severity Rating Scale (C-SSRS) at screening or anytime during study participation;
- Have a positive urine screen for any substances, including cannabis
- Have a breathalyzer reading above 0.000 g/dl;
- Be pregnant, nursing, or planning to become pregnant while taking part in the study;
- Have a medical condition that may interfere with safe study participation;
- Have clinically significant abnormalities on the EKG;
- Have evidence of renal impairment, defined by an eGFR value of <90 ml/min;
- Have evidence of hepatic impairment, defined by a score of ≥5 points on the Child-Pugh assessment of liver function;
- Exceed Grade 2 laboratory or vital sign abnormalities, based on FDA Guidance Document "Toxicity Grading Scale for Healthy Adult and Adolescent Volunteers Enrolled in Preventive Vaccine Clinical Trials";
- Have past month use of cannabis or cannabis products;
- Have past month use of electronic nicotine delivery system (ENDS);
- Have use of any medications (other than methods of birth control as listed in inclusion criteria for female participants) within 14 days or 5 half-lives (whichever is longer) prior to study drug administration, and throughout the study, including medication for smoking cessation, any prescription, OTC, dietary supplements, herbal products, or vitamins;
- Have any other circumstances that, in the opinion of the investigators, would not be a good fit for study participation.
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione incrociata
- Mascheramento: Triplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Δ9-THCV first, then placebo.
Participants will first take a 10mg Δ9-THCV gummy once a day for 5 days.
After a 14-day washout period, participants will take a matched placebo gummy (0mg Δ9-THCV) once a day for 5 days.
|
10mg Δ9-Tetrahydrocannabivarin oral gummy
Matched Placebo (oral gummy, 0mg Δ9-Tetrahydrocannabivarin)
|
|
Sperimentale: Placebo first, then THCV
Participants will take a placebo gummy (0mg Δ9-THCV) once a day for 5 days.
After a 14-day washout period, participants will take a 10mg Δ9-THCV gummy once a day for 5 days.
|
10mg Δ9-Tetrahydrocannabivarin oral gummy
Matched Placebo (oral gummy, 0mg Δ9-Tetrahydrocannabivarin)
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Latency to initiate smoking
Lasso di tempo: Assessed during each 5-day medication condition, following overnight abstinence on Day 5
|
Participants will complete the McKee Smoking Lapse Task following overnight abstinence to assess the effects of oral Δ9-THCV (10 mg), compared with placebo, on the ability to resist smoking.
The primary outcome is latency to initiate smoking during the 50-minute delay period, defined as the number of minutes participants delay smoking their first cigarette (range: 0-50 minutes).
|
Assessed during each 5-day medication condition, following overnight abstinence on Day 5
|
|
Number of cigarettes smoked during self-administration
Lasso di tempo: Assessed during each 5-day medication condition, following overnight abstinence on Day 5
|
Participants will complete the McKee Smoking Lapse Task following overnight abstinence to assess the effects of oral Δ9-THCV (10 mg), compared with placebo, on cigarette self-administration.
The outcome is the number of cigarettes smoked during the 60-minute self-administration period of the task (no set range).
|
Assessed during each 5-day medication condition, following overnight abstinence on Day 5
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Questionnaire of Smoking Urges-Brief total score
Lasso di tempo: Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence
|
Participants will complete the 10-item Questionnaire of Smoking Urges-Brief (QSU-Brief) during the McKee Smoking Lapse Task to assess cigarette craving.
The QSU-Brief assesses urges and cravings using a 7-point Likert response scale, with higher scores indicating greater craving (range: 10-70).
Cue-induced cigarette craving in response to cigarette (vs.
neutral) cues will be calculated and compared between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence
|
|
Minnesota Nicotine Withdrawal Scale score
Lasso di tempo: Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence
|
Participants will complete ratings of nicotine withdrawal following overnight abstinence using the 8-item Minnesota Nicotine Withdrawal Scale (MNWS), with higher values indicating more severe withdrawal (range: 0-32).
Differences in MNWS scores will be evaluated between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence
|
|
Modified Cigarette Evaluation Questionnaire satisfaction score
Lasso di tempo: Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
Participants will complete the 12-item Modified Cigarette Evaluation Questionnaire (mCEQ) during the cigarette self-administration period of the McKee Smoking Lapse Task to assess satisfaction associated with smoking.
Items are rated on a 7-point scale, with higher scores indicating greater endorsement.
The satisfaction subscale score is calculated as the sum of Items 1, 2, and 12 (range: 3-21).
Differences in satisfaction scores will be evaluated between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
|
Modified Cigarette Evaluation Questionnaire psychological reward score
Lasso di tempo: Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
Participants will complete the 12-item Modified Cigarette Evaluation Questionnaire (mCEQ) during the cigarette self-administration period of the McKee Smoking Lapse Task to assess psychological reward associated with smoking.
Items are rated on a 7-point scale, with higher scores indicating greater endorsement.
The psychological reward subscale score is calculated as the sum of Items 4, 5, 6, 7, 8 (range: 5-35).
Differences in psychological reward scores will be evaluated between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
|
Modified Cigarette Evaluation Questionnaire nausea/dizziness score
Lasso di tempo: Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
Participants will complete the 12-item Modified Cigarette Evaluation Questionnaire (mCEQ) during the cigarette self-administration period of the McKee Smoking Lapse Task to assess nausea and dizziness associated with smoking.
Items are rated on a 7-point scale, with higher scores indicating greater endorsement.
The nausea/dizziness subscale score is calculated as the sum of Items 9 and 10 (range: 2-14).
Differences in nausea/dizziness scores will be evaluated between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
|
Modified Cigarette Evaluation Questionnaire craving relief score
Lasso di tempo: Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
Participants will complete the 12-item Modified Cigarette Evaluation Questionnaire (mCEQ) during the cigarette self-administration period of the McKee Smoking Lapse Task to assess craving relief associated with smoking.
Items are rated on a 7-point scale, with higher scores indicating greater endorsement.
The craving relief subscale score is based on Item 11 (range: 1-7).
Differences in craving relief scores will be evaluated between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
|
Modified Cigarette Evaluation Questionnaire enjoyment of airway sensations score
Lasso di tempo: Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
Participants will complete the 12-item Modified Cigarette Evaluation Questionnaire (mCEQ) during the cigarette self-administration period of the McKee Smoking Lapse Task to assess the enjoyment of airway sensations associated with smoking.
Items are rated on a 7-point scale, with higher scores indicating greater endorsement.
The enjoyment of airway sensations subscale score is based on Item 3 (range: 1-7).
Differences in enjoyment of airway sensations scores will be evaluated between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Collaboratori
Investigatori
- Investigatore principale: Lara A Ray, PhD, University of California, Los Angeles
- Investigatore principale: Erica N Grodin, PhD, University of California, Los Angeles
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Stimato)
1 luglio 2026
Completamento primario (Stimato)
31 maggio 2028
Completamento dello studio (Stimato)
31 maggio 2028
Date di iscrizione allo studio
Primo inviato
26 maggio 2026
Primo inviato che soddisfa i criteri di controllo qualità
2 giugno 2026
Primo Inserito (Effettivo)
9 giugno 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
9 giugno 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
2 giugno 2026
Ultimo verificato
1 giugno 2026
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- IRB-26-1097
- R21DA059769 (Sovvenzione/contratto NIH degli Stati Uniti)
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Sì
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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