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- Klinische proef NCT07699120
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
Conditie
Interventie / Behandeling
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:
Oral liquid placebo product manufactured according to cGMP
|
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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:
|
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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:
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
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Pre-dose up to 144 hours following the final dose
|
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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
|
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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
|
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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
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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
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- RPC25PH101
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 .