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Evaluation of BRC-002 Safety, Tolerability, Pharmacokinetics, and Food Effects in Healthy Participants

7 de julio de 2026 actualizado por: Biopharmaceutical Research Company

A Phase 1, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose and Repeat Dose and Randomized, Open-label, Crossover, Food Effect Safety, Tolerability, and Pharmacokinetic Study of BRC-002 in Healthy Participants

This study will evaluate the safety and tolerability of BRC-002, an investigational botanical drug from cannabis, in healthy adults. The study will also assess how the body processes BRC-002 and whether taking it with food affects how it is absorbed or metabolized. The results of this study will help support further clinical development of BRC-002 and guide dose selection in patient populations.

Descripción general del estudio

Estado

Inscripción por invitación

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Estimado)

50

Fase

  • Fase 1

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.

Ubicaciones de estudio

    • Ontario
      • Toronto, Ontario, Canadá, M9L 3A2
        • Bio Pharma Research Inc.

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

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  • Male and female volunteers, 18-55 years of age, inclusive.
  • Body mass index (BMI) ≥ 20 and ≤ 35 kg/m2, inclusive, and weight ≥50 kg.
  • Healthy, according to medical history, ECG, vital signs, laboratory results and physical examination.
  • No clinically significant abnormalities in laboratory values.
  • Ability to comprehend and be informed of the nature of the study; capable of giving written informed consent prior to any study related procedure.
  • Ability to fast for at least 14 hours and consume standard meals and/or high-fat, high-calorie meal, as applicable.
  • Agree to avoid use of cannabis or cannabis products for the duration of the study.
  • Non-pregnant, non-lactating, and agree to use an approved method of contraception, if applicable.

Exclusion Criteria:

  • Known history or presence of any clinically significant hepatic, renal/genitourinary, gastrointestinal, cardiovascular, cerebrovascular, pulmonary, endocrine, immunological (including immunocompromising), musculoskeletal, neurological, psychiatric, dermatological or hematological disease or condition.
  • Personal or significant family history of seizure disorder, neurodegenerative disease, brain trauma, brain infection, or any other condition known to increase the risk of seizures.
  • Presence of any clinically significant illness within 30 days prior to first dosing.
  • Known history or positive test result for human immunodeficiency virus (HIV), chronic Hepatitis B surface antigen, or Hepatitis C.
  • Smoking and/or use of any nicotine-containing products (e.g., vapes, e-cigarettes, gum, lozenges, patches, chewing tobacco, oral pouches, etc.) within 6 months prior to study drug administration.
  • Positive test result for drugs of abuse (THC, amphetamines, barbiturates, cocaine, opiates, phencyclidine and benzodiazepines), alcohol, or cotinine.
  • Positive pregnancy test for female participants.
  • Lifetime history of cannabis dependence.
  • Use of cannabis or cannabis products (including hemp or CBD products) within the past 30 days prior to Screening.
  • Lifetime history of major psychiatric illness, including schizophrenia, bipolar disorder, generalized anxiety disorder, major depression, panic disorder, substance use disorder, or psychosis.
  • Current suicidal ideation or past suicide attempt.
  • History of allergy, hypersensitivity, or intolerance to cannabis, CBD, or related products.
  • Past significant adverse reaction (allergic, anaphylactic, hypersensitivity, angioedema) or severe response to study drugs, their excipients, and to any other clinically significant drug or food.
  • Evidence of significant hepatic impairment as determined by clinically significant abnormalities in laboratory values.
  • Known history or presence of alcohol abuse or dependence within one year prior to first study drug administration; drug abuse or dependence; presence of any clinically significant dietary restrictions.
  • Abnormal diet patterns during the four weeks preceding the study.
  • Intolerance to and/or difficulty with blood sampling through venipuncture.
  • Recent blood donation (50-499 mL in the previous 30 days or 500 mL or more in the previous 56 days prior to first study drug administration).
  • Recent plasma donation by plasmapheresis (within 7 days prior to first study drug administration).
  • Individuals who have participated in another clinical trial or who received an investigational drug within 30 days prior to first study drug administration.
  • Use of any enzyme-modifying drugs and/or other products, including strong inhibitors or inducers of cytochrome P450 (CYP) enzymes in the previous 30 days before first study drug administration.
  • Use of any monoamine oxidase (MAO) inhibitors within 30 days prior to first study drug administration.
  • Use of clobazam, valproate, or mTOR inhibitors within 30 days prior to first study drug administration.
  • Use of any prescription medication or over-the-counter medications (including oral multivitamins, dietary and/or herbal supplements and teas) within 14 days prior to first study drug administration, except for medically acceptable contraceptive products.
  • Consumption of food or beverages containing grapefruit, Seville oranges, pineapple and/or pomelo within 10 days prior to first study drug administration.
  • Consumption of food or beverages containing caffeine/methylxanthines, poppy seeds, and/or alcohol within 48 hours before dosing.
  • Any major surgery within 6 months prior to the start of the study.
  • Difficulty with oral drug administration.
  • Unable or unwilling to provide informed consent.
  • Tattoo or body piercing within 30 days prior to first study drug administration.
  • Any other conditions that, in the opinion of the PI/Sub-Investigator or Sponsor, would make the participant unsuitable for inclusion, or could interfere with the participant participating in or completing the study.

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 paralela
  • Enmascaramiento: Cuadruplicar

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Single Ascending Dose (SAD)
Single Ascending Dose (SAD) study to evaluate the safety, tolerability and pharmacokinetics of increasing single doses of BRC-002 vs. placebo
Oral liquid standardized cannabis-derived botanical drug product manufactured according to cGMP
Otros nombres:
  • botanical drug from cannabis
Oral liquid placebo product manufactured according to cGMP
Experimental: Food Effect (FE)
Food Effect (FE) study to evaluate the impact of a high-fat, high-calorie meal on the safety, tolerability and pharmacokinetics of BRC-002.
Oral liquid standardized cannabis-derived botanical drug product manufactured according to cGMP
Otros nombres:
  • botanical drug from cannabis
Experimental: Repeat Dose (RD)
Repeat Dose (RD) study to evaluate the safety, tolerability and pharmacokinetics of repeated doses of BRC-002 vs. placebo
Oral liquid standardized cannabis-derived botanical drug product manufactured according to cGMP
Otros nombres:
  • botanical drug from cannabis
Oral liquid placebo product manufactured according to cGMP

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Safety and tolerability of BRC-002 after single and multiple dose administration in healthy participants
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Incidence of adverse events, including serious AEs and AEs of special interest. Clinically significant changes in clinical laboratory tests, vital signs, electrocardiograms, and physical examinations.
Pre-dose up to 144 hours following the final dose

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Maximum Observed Plasma Concentration (Cmax)
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Maximum observed plasma concentration of BRC-002 following administration
Pre-dose up to 144 hours following the final dose
Dose-Normalized Maximum Observed Plasma Concentration (Cmax_D)
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Maximum observed plasma concentration of BRC-002 normalized to the administered dose
Pre-dose up to 144 hours following the final dose
Time to Maximum Plasma Concentration (tmax)
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Time from dosing to the maximum observed plasma concentration of BRC-002
Pre-dose up to 144 hours following the final dose
Area Under the Plasma Concentration-Time Curve From 0 Hours to the Time of the Last Quantifiable Concentration (AUC0-tlast)
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Area under the plasma concentration-time curve of BRC-002 from time zero to the last quantifiable concentration
Pre-dose up to 144 hours following the final dose
Dose-Normalized Area Under the Plasma Concentration-Time Curve From 0 Hours to the Time of the Last Quantifiable Concentration (AUC0-tlast_D)
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Area under the plasma concentration-time curve of BRC-002 from time zero to the last quantifiable concentration, normalized to the administered dose
Pre-dose up to 144 hours following the final dose
Area Under the Plasma Concentration-Time Curve From 0 Hours to Infinity (AUC0-inf)
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Area under the plasma concentration-time curve of BRC-002 from time zero extrapolated to infinity
Pre-dose up to 144 hours following the final dose
Dose-Normalized Area Under the Plasma Concentration-Time Curve From 0 Hours to Infinity (AUC0-inf_D)
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Area under the plasma concentration-time curve of BRC-002 from time zero extrapolated to infinity, normalized to the administered dose
Pre-dose up to 144 hours following the final dose
Apparent Volume of Distribution During the Terminal Elimination Phase (Vd/F)
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Apparent volume of distribution of BRC-002 during the terminal elimination phase following extravascular administration
Pre-dose up to 144 hours following the final dose
Apparent Oral Clearance From Plasma (CL/F)
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Apparent clearance of BRC-002 from plasma following extravascular administration
Pre-dose up to 144 hours following the final dose
Apparent Elimination Half-Life (t½)
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Time required for the plasma concentration of BRC-002 to decrease by half during the terminal elimination phase
Pre-dose up to 144 hours following the final dose
Apparent Terminal Elimination Rate Constant (λz)
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Terminal elimination rate constant of BRC-002 estimated from the terminal log-linear portion of the plasma concentration-time curve
Pre-dose up to 144 hours following the final dose
Percentage of AUC Extrapolated From the Last Quantifiable Concentration to Infinity (AUC%extrap)
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Percentage of the total area under the plasma concentration-time curve of BRC-002 from time zero to infinity that is extrapolated from the last quantifiable concentration to infinity
Pre-dose up to 144 hours following the final dose
Maximum Observed Plasma Concentration (Cmax) Under Fasted and Fed Conditions
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Maximum observed plasma concentration of BRC-002 following administration under fasted and fed (high-fat/high-calorie meal) conditions
Pre-dose up to 144 hours following the final dose
Area Under the Plasma Concentration-Time Curve From 0 Hours to the Time of the Last Quantifiable Concentration (AUC0-tlast) Under Fasted and Fed Conditions
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Area under the plasma concentration-time curve of BRC-002 from time zero to the last quantifiable concentration following administration under fasted and fed (high-fat/high-calorie meal) conditions
Pre-dose up to 144 hours following the final dose
Area Under the Plasma Concentration-Time Curve From 0 Hours to Infinity (AUC0-inf) Under Fasted and Fed Conditions
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Area under the plasma concentration-time curve of BRC-002 from time zero extrapolated to infinity following administration under fasted and fed (high-fat/high-calorie meal) conditions
Pre-dose up to 144 hours following the final dose
Time to Maximum Plasma Concentration (tmax) Under Fasted and Fed Conditions
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Time from dosing to the maximum observed plasma concentration of BRC-002 following administration under fasted and fed (high-fat/high-calorie meal) conditions
Pre-dose up to 144 hours following the final dose
Apparent Elimination Half-Life (t½) Under Fasted and Fed Conditions
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Time required for the plasma concentration of BRC-002 to decrease by half during the terminal elimination phase following administration under fasted and fed (high-fat/high-calorie meal) conditions
Pre-dose up to 144 hours following the final dose
Apparent Terminal Elimination Rate Constant (λz) Under Fasted and Fed Conditions
Periodo de tiempo: Pre-dose up to 144 hours following the final dose
Terminal elimination rate constant of BRC-002 estimated from the terminal log-linear portion of the plasma concentration-time curve following administration under fasted and fed (high-fat/high-calorie meal) conditions
Pre-dose up to 144 hours following the final dose

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

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 (Actual)

15 de junio de 2026

Finalización primaria (Estimado)

1 de octubre de 2026

Finalización del estudio (Estimado)

1 de noviembre de 2026

Fechas de registro del estudio

Enviado por primera vez

2 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

7 de julio de 2026

Publicado por primera vez (Actual)

13 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

13 de julio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

7 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • RPC25PH101

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan IPD

Only IPD used in the publication of study results

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

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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