- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07699120
Evaluation of BRC-002 Safety, Tolerability, Pharmacokinetics, and Food Effects in Healthy Participants
2026년 7월 7일 업데이트: 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.
연구 개요
연구 유형
중재적
등록 (추정된)
50
단계
- 1단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
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Ontario
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Toronto, Ontario, 캐나다, M9L 3A2
- Bio Pharma Research Inc.
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참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
- 성인
건강한 자원 봉사자를 받아들입니다
예
설명
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.
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 네 배로
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: 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
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Oral liquid standardized cannabis-derived botanical drug product manufactured according to cGMP
다른 이름들:
Oral liquid placebo product manufactured according to cGMP
|
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실험적: 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.
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Oral liquid standardized cannabis-derived botanical drug product manufactured according to cGMP
다른 이름들:
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실험적: Repeat Dose (RD)
Repeat Dose (RD) study to evaluate the safety, tolerability and pharmacokinetics of repeated doses of BRC-002 vs. placebo
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Oral liquid standardized cannabis-derived botanical drug product manufactured according to cGMP
다른 이름들:
Oral liquid placebo product manufactured according to cGMP
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Safety and tolerability of BRC-002 after single and multiple dose administration in healthy participants
기간: 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.
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Pre-dose up to 144 hours following the final dose
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Maximum Observed Plasma Concentration (Cmax)
기간: Pre-dose up to 144 hours following the final dose
|
Maximum observed plasma concentration of BRC-002 following administration
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Pre-dose up to 144 hours following the final dose
|
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Dose-Normalized Maximum Observed Plasma Concentration (Cmax_D)
기간: 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
|
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Time to Maximum Plasma Concentration (tmax)
기간: Pre-dose up to 144 hours following the final dose
|
Time from dosing to the maximum observed plasma concentration of BRC-002
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Pre-dose up to 144 hours following the final dose
|
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Area Under the Plasma Concentration-Time Curve From 0 Hours to the Time of the Last Quantifiable Concentration (AUC0-tlast)
기간: Pre-dose up to 144 hours following the final dose
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Area under the plasma concentration-time curve of BRC-002 from time zero to the last quantifiable concentration
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Pre-dose up to 144 hours following the final dose
|
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Dose-Normalized Area Under the Plasma Concentration-Time Curve From 0 Hours to the Time of the Last Quantifiable Concentration (AUC0-tlast_D)
기간: 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
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Pre-dose up to 144 hours following the final dose
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Area Under the Plasma Concentration-Time Curve From 0 Hours to Infinity (AUC0-inf)
기간: 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
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Pre-dose up to 144 hours following the final dose
|
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Dose-Normalized Area Under the Plasma Concentration-Time Curve From 0 Hours to Infinity (AUC0-inf_D)
기간: 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
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Pre-dose up to 144 hours following the final dose
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Apparent Volume of Distribution During the Terminal Elimination Phase (Vd/F)
기간: Pre-dose up to 144 hours following the final dose
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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)
기간: 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)
기간: 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
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Pre-dose up to 144 hours following the final dose
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Apparent Terminal Elimination Rate Constant (λz)
기간: Pre-dose up to 144 hours following the final dose
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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)
기간: 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
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Pre-dose up to 144 hours following the final dose
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Maximum Observed Plasma Concentration (Cmax) Under Fasted and Fed Conditions
기간: 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
|
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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
기간: 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
|
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Area Under the Plasma Concentration-Time Curve From 0 Hours to Infinity (AUC0-inf) Under Fasted and Fed Conditions
기간: 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
기간: 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
|
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Apparent Elimination Half-Life (t½) Under Fasted and Fed Conditions
기간: 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
|
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Apparent Terminal Elimination Rate Constant (λz) Under Fasted and Fed Conditions
기간: 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
|
공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
간행물 및 유용한 링크
연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (실제)
2026년 6월 15일
기본 완료 (추정된)
2026년 10월 1일
연구 완료 (추정된)
2026년 11월 1일
연구 등록 날짜
최초 제출
2026년 7월 2일
QC 기준을 충족하는 최초 제출
2026년 7월 7일
처음 게시됨 (실제)
2026년 7월 13일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2026년 7월 13일
QC 기준을 충족하는 마지막 업데이트 제출
2026년 7월 7일
마지막으로 확인됨
2026년 7월 1일
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .