- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07699120
Evaluation of BRC-002 Safety, Tolerability, Pharmacokinetics, and Food Effects in Healthy Participants
7 juillet 2026 mis à jour par: 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.
Aperçu de l'étude
Statut
Inscription sur invitation
Les conditions
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Estimé)
50
Phase
- La phase 1
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
-
-
Ontario
-
Toronto, Ontario, Canada, M9L 3A2
- Bio Pharma Research Inc.
-
-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
Oui
La description
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 d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Quadruple
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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
Autres noms:
Oral liquid placebo product manufactured according to cGMP
|
|
Expérimental: 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
Autres noms:
|
|
Expérimental: 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
Autres noms:
Oral liquid placebo product manufactured according to cGMP
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Safety and tolerability of BRC-002 after single and multiple dose administration in healthy participants
Délai: 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
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Maximum Observed Plasma Concentration (Cmax)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
15 juin 2026
Achèvement primaire (Estimé)
1 octobre 2026
Achèvement de l'étude (Estimé)
1 novembre 2026
Dates d'inscription aux études
Première soumission
2 juillet 2026
Première soumission répondant aux critères de contrôle qualité
7 juillet 2026
Première publication (Réel)
13 juillet 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
13 juillet 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
7 juillet 2026
Dernière vérification
1 juillet 2026
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- RPC25PH101
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
OUI
Description du régime IPD
Only IPD used in the publication of study results
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Oui
Étudie un produit d'appareil réglementé par la FDA américaine
Non
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