- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07636356
THCV Treatment for Smokers
3 de agosto de 2026 actualizado por: 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).
Descripción general del estudio
Estado
Aún no reclutando
Condiciones
Intervención / Tratamiento
Descripción detallada
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 de estudio
Intervencionista
Inscripción (Estimado)
32
Fase
- Fase 2
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Estudio Contacto
- Nombre: Jessica Jenkins, MS
- Número de teléfono: 310-206-6756
- Correo electrónico: jenkinsj@ucla.edu
Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Descripción
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.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación cruzada
- Enmascaramiento: Triple
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: 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)
|
|
Experimental: 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)
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Latency to initiate smoking
Periodo de tiempo: 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
Periodo de tiempo: 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
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Questionnaire of Smoking Urges-Brief total score
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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.
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Lara A Ray, PhD, University of California, Los Angeles
- Investigador principal: Erica N Grodin, PhD, University of California, Los Angeles
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Estimado)
1 de octubre de 2026
Finalización primaria (Estimado)
31 de mayo de 2028
Finalización del estudio (Estimado)
31 de mayo de 2028
Fechas de registro del estudio
Enviado por primera vez
26 de mayo de 2026
Primero enviado que cumplió con los criterios de control de calidad
2 de junio de 2026
Publicado por primera vez (Actual)
9 de junio de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
4 de agosto de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
3 de agosto de 2026
Última verificación
1 de agosto de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- IRB-26-1097
- R21DA059769 (Subvención/contrato del NIH de EE. UU.)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Sí
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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