- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT07699120
Evaluation of BRC-002 Safety, Tolerability, Pharmacokinetics, and Food Effects in Healthy Participants
7 июля 2026 г. обновлено: 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.
Обзор исследования
Статус
Запись по приглашению
Условия
Вмешательство/лечение
Тип исследования
Интервенционный
Регистрация (Оцененный)
50
Фаза
- Фаза 1
Контакты и местонахождение
В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.
Места учебы
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Ontario
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Toronto, Ontario, Канада, M9L 3A2
- Bio Pharma Research Inc.
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Критерии участия
Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.
Критерии приемлемости
Возраст, подходящий для обучения
- Взрослый
Принимает здоровых добровольцев
Да
Описание
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.
Учебный план
В этом разделе представлена подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Четырехместный
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Экспериментальный: 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
Другие имена:
Oral liquid placebo product manufactured according to cGMP
|
|
Экспериментальный: 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
Другие имена:
|
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Экспериментальный: 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
Другие имена:
Oral liquid placebo product manufactured according to cGMP
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Safety and tolerability of BRC-002 after single and multiple dose administration in healthy participants
Временное ограничение: 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
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Maximum Observed Plasma Concentration (Cmax)
Временное ограничение: 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)
Временное ограничение: 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)
Временное ограничение: 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)
Временное ограничение: 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)
Временное ограничение: 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)
Временное ограничение: 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)
Временное ограничение: 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)
Временное ограничение: 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)
Временное ограничение: Pre-dose up to 144 hours following the final dose
|
Apparent clearance of BRC-002 from plasma following extravascular administration
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Pre-dose up to 144 hours following the final dose
|
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Apparent Elimination Half-Life (t½)
Временное ограничение: 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)
Временное ограничение: 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
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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)
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
|
Соавторы и исследователи
Здесь вы найдете людей и организации, участвующие в этом исследовании.
Публикации и полезные ссылки
Лицо, ответственное за внесение сведений об исследовании, добровольно предоставляет эти публикации. Это может быть что угодно, связанное с исследованием.
Полезные ссылки
Даты записи исследования
Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.
Изучение основных дат
Начало исследования (Действительный)
15 июня 2026 г.
Первичное завершение (Оцененный)
1 октября 2026 г.
Завершение исследования (Оцененный)
1 ноября 2026 г.
Даты регистрации исследования
Первый отправленный
2 июля 2026 г.
Впервые представлено, что соответствует критериям контроля качества
7 июля 2026 г.
Первый опубликованный (Действительный)
13 июля 2026 г.
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
13 июля 2026 г.
Последнее отправленное обновление, отвечающее критериям контроля качества
7 июля 2026 г.
Последняя проверка
1 июля 2026 г.
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- RPC25PH101
Планирование данных отдельных участников (IPD)
Планируете делиться данными об отдельных участниках (IPD)?
ДА
Описание плана IPD
Only IPD used in the publication of study results
Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Да
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
Нет
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .