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

7 juli 2026 bijgewerkt door: 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.

Studie Overzicht

Toestand

Aanmelden op uitnodiging

Studietype

Ingrijpend

Inschrijving (Geschat)

50

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

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

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen

Accepteert gezonde vrijwilligers

Ja

Beschrijving

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.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Verviervoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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
Andere namen:
  • botanical drug from cannabis
Oral liquid placebo product manufactured according to cGMP
Experimenteel: 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
Andere namen:
  • botanical drug from cannabis
Experimenteel: 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
Andere namen:
  • botanical drug from cannabis
Oral liquid placebo product manufactured according to cGMP

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Safety and tolerability of BRC-002 after single and multiple dose administration in healthy participants
Tijdsspanne: 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

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Maximum Observed Plasma Concentration (Cmax)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

15 juni 2026

Primaire voltooiing (Geschat)

1 oktober 2026

Studie voltooiing (Geschat)

1 november 2026

Studieregistratiedata

Eerst ingediend

2 juli 2026

Eerst ingediend dat voldeed aan de QC-criteria

7 juli 2026

Eerst geplaatst (Werkelijk)

13 juli 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

13 juli 2026

Laatste update ingediend die voldeed aan QC-criteria

7 juli 2026

Laatst geverifieerd

1 juli 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

JA

Beschrijving IPD-plan

Only IPD used in the publication of study results

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Ja

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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