INTERVENTIONALCOMPLETEDNCT07186283

A Phase 1 Study to Assess the Safety and Pharmacokinetics of Novel Cannabidiol (CBD) Soft-gel Capsule Formulation (NW300EMCBD) in Healthy Subjects

The purpose of this study is to test a new formulation of cannabidiol (CBD) to see how it is processed in the body and how safe it is for healthy volunteers. CBD is a compound found in the cannabis plant that has shown potential to help treat various medical and mental health conditions. While there is already an approved CBD-based drug that is used for epilepsy in the UK, called Epidyolex, most CBD formulations have poor absorption when taken orally, reducing their effectiveness and often requiring higher doses. NW PharmaTech has developed a new CBD formulation aimed at improving absorption and processing by the body. This study will assess the absorption, safety, and tolerability of two different doses (600 mg and 900 mg) of the new formulation and will compare them with Epidyolex (dosed as per approved label). All participants will receive each of the following three dosing regimens in a randomised order across three separate experimental periods, with each period separated by a 25 day washout period, which ensures that the drug from one dosing regimen is fully cleared from your body before the next dosing regimen begins. Regimen A: 600 mg of the new CBD formulation (NW300EMCBD) administered orally Regimen B: 900 mg of the new CBD formulation (NW300EMCBD) administered orally Regimen C: 25 mg/kg Epidyolex solution (2 x 12.5 mg/kg doses separated by 12 hours) administered orally In total, participants will complete three dosing visits (one per experimental period), each spaced 25 days apart. The study will evaluate the pharmacokinetics (PK) of the formulations, which refers to how the body absorbs, distributes, metabolizes, and eliminates the drugs.

Locally preserved from ClinicalTrials.govOpen ClinicalTrials.govlast source update 2026-02-02

What this record can show

Protocol only - no registry results posted

This locally preserved record separates the registered protocol from source-reported registry results. Neither is a treatment recommendation.

Registry facts

Study at a glance

Phase: PHASE1
Enrollment: 14 (ACTUAL)
Start date: 2025-09-22
Sponsor: NW PharmaTech Ltd
Design: RANDOMIZED · CROSSOVER · TREATMENT
Locations: 1
Results record: Not present in registry snapshot

Linked local records

Related local records

Local links use governed condition terms or exact source-reported intervention names. They are navigation candidates, not efficacy claims.

Conditions

No published condition report matched.

Cannabinoids and active compounds

Medicines

Epidyolex Epidyolex

Interventions

What was registered

DRUG

CBD soft-gel capsules 600 mg

600 mg

DRUG

CBD soft-gel capsules 900 mg

900 mg

DRUG

Epidyolex

25 mg/kg

Eligibility

Population and criteria

Sex: ALL
Minimum age: 18 Years
Maximum age

Inclusion criteria

1. Healthy male or female volunteers. 2. Age range between 18 and 55 years old. 3. Weight at least 50kg and have a body mass index (BMI) between 19 and 30 kg/m2 at screening. 4. Willingness to comply with and complete all study procedures, including consuming the protocol specified high-fat, high-calorie meal in 30 minutes. 5. In good health, as determined by no clinically significant findings from medical history, 12-lead ECG and vital signs measurements, and clinical laboratory evaluations at screening and check-in, and from the physical examination at screening and symptom-directed physical examination at baseline, as assessed by the investigator or designee. 6. Abstinence from consuming St John's wort, grapefruit (juice), alcohol or tobacco and nicotine products for at least 72 hours prior to dosing and throughout treatment period. 7. Abstinence from caffeine for the duration of the in-clinic confinement period, including all dosing days. Caffeinated beverages and products will not be available on site. 8. Capable and willing to comply with protocol requirements during the study. 9. Participant is willing and able to give informed consent for participation in the study.

Exclusion criteria

1. Participation in a research clinical trial within 90 days prior to Day 1 of the first experimental period, or 5 elimination half-lives prior to Day 1 of the first experimental period (whichever is longer) to Day 1, or throughout the study. 2. Use of cannabis products, including hemp, in any form (including medication, oils, edibles or drinks) during the last 28 days before screening. 3. History of hypersensitivity or allergy to CBD oil, sesame oil, hemp or any other cannabinoid products, or any of the items that could be included in the standardized meals/snacks. 4. Using any regular medication in the 28 days prior to screening and throughout the study (as required doses of paracetamol or non-steroidal anti-inflammatory drugs (NSAIDs) are permitted). 5. Abnormal screening sample: clinically significant liver, renal or haematological abnormalities, including total Bilirubin, ALT or AST \> the upper limit of normal (ULN). 6. Positive screening test indicating active infection with HIV, hepatitis B virus or hepatitis C virus. Participants with evidence of past HBV infection and complete recovery may be eligible, at the discretion of the Investigator, provided liver function tests are within normal limits and there is no evidence of active infection. 7. Positive urine drug sample, including THC, at screening and, baseline excluding THC at post-dose. 8. Positive alcohol breathalyser test at screening and throughout the study. 9. Any suicidal ideation or behaviour in the past 12 months as assessed by responses to Columbia Suicidal Severity Rating questionnaire at screening. 10. Any history of mental disorder including major depressive disorder, bipolar disorder, psychosis, and any current substance use disorder, including alcohol and tobacco use disorder. 11. Any self-reported, observed or assessed medical condition that might put the subject at risk according to the physician's opinion. 12. Any significant previous or current history of comorbidities capable of significantly altering the absorption, metabolism, or elimination of drugs; of constituting a risk when taking the investigational product; or of interfering with the interpretation of data. 13. Participants with a sitting blood pressure at screening, after resting for 5 minutes, higher than 140/90 mmHg or lower than 90/50 mmHg. 14. Blood donation or loss (eg surgery) over 200 ml in 3 months prior to screening and throughout study (menstruation is acceptable). 15. Male participants not willing to use contraceptive methods throughout the study. 16. Female participants who are pregnant (positive B-hCG urine test), lactating or breastfeeding. 17. Female participants of childbearing potential\* and not willing to use highly effective contraceptive methods\*\* at screening or throughout the study. \*Defined as females who have experienced menarche and are not surgically sterilised (eg hysterectomy, bilateral salpingectomy) or post-menopausal. \*\*Highly effective methods of birth control are those with a failure rate \<1% per year and include combined oestrogen and progesterone hormonal contraception, progestogen-only hormonal contraception, intrauterine devices (IUD), intrauterine hormone-releasing systems (IUS) and vasectomised partner. 18. Participants with planned surgical or medical treatment requiring hospitalisation during the study. 19. Employees or family members of the Sponsor. 20. Participant unable to communicate reliably with research team. 21. Participant is not able to swallow capsules. 22. Subject unable or unwilling to consume the protocol specified high fat meal required by the trial protocol and/or the soft gel capsules, which contain gelatine of bovine origin, and/or Epidyolex which contains sesame oil and ethanol. 23. Subjects with alcohol consumption \> 14U/ week.

secondary outcomes

secondary measures

Total Area Under the Curve (AUCinf)

Time frame: Pre-dose up to 192 hours post dose

Difference in CBD total exposure between the novel formulation and Epidyolex

Total Area Under the Curve (AUCt)

Time frame: Pre-dose up to 192 hours post dose

Difference in CBD total exposure between the novel formulation and Epidyolex

Dose-normalised Total Area Under the Curve (AUCinf/D)

Time frame: Pre-dose up to 192 hours post dose

Difference in CBD total exposure normalised by administered CBD total dose between the novel formulation and Epidyolex

Cmax

Time frame: Pre-dose up to 192 hours post dose

Maximum plasma concentration

Tmax

Time frame: Pre-dose up to 192 hours post dose

Time to reach maximum plasma concentration

Plasma Half-life (t½)

Time frame: Pre-dose up to 192 hours post dose

Time to reduce the plasma concentration by half

Apparent plasma clearance (CL/F)

Time frame: Pre-dose up to 192 hours post dose

Apparent volume of distribution (Vz/F)

Time frame: Pre-dose up to 192 hours post dose

Elimination rate constant (Kel)

Time frame: Pre-dose up to 192 hours post dose

Number of participants with Adverse Events (AEs)

Time frame: Pre-dose up to 192 hours post dose

Changes from pre-dose baseline in laboratory findings

Time frame: Pre-dose up to 192 hours post dose

laboratory sampling

Changes from pre-dose baseline Blood Pressure (BP)

Time frame: Pre-dose up to 192 hours post dose

Changes from pre-dose baseline in Heart Rate (HR)

Time frame: Pre-dose up to 192 hours post dose

Changes from pre-dose baseline in vital signs Respiratory Rate

Time frame: Pre-dose up to 192 hours post dose

Changes from pre-dose baseline in Body Temperature

Time frame: Pre-dose up to 192 hours post dose

Number of participants with ECG findings

Time frame: Pre-dose up to 192 hours post dose

Changes from pre-dose baseline iGastrointestinal Symptom Rating Scale (GSRS) score

Time frame: Pre-dose to 24 hours post dose

The GSRS is a 15-item rating scale, where each item is assessed with a 7-point Likert scale, with higher scores indicating more severe symptoms.

Number of participants with suicidal ideation and/or behavior as assessed by Columbia-Suicide Severity Rating Scale (C-SSRS)

Time frame: Pre-dose up to 192 hours post dose

The Columbia-Suicide Severity Rating Scale (C-SSRS) is a clinician administered assessment tool that evaluates suicidal ideation and behavior. Number of participants that have an affirmative response provided to the 5 items for suicidal ideation (1. Wish to be dead, 2. Non-specific active suicidal thoughts, 3. Active suicidal ideation with any methods (not plan) without intent to act, 4. Active suicidal ideation with some intent to act, without specific plan, 5. Active suicidal ideation with specific plan and intent) and/or to the 6 items for suicidal behavior (1. Actual attempt, 2. Interrupted attempt, 3. Aborted attempt, 4. Preparatory acts or behavior, 5. Suicidal Behavior 6. Completed suicide,) will be reported.

A Phase 1 Study to Assess the Safety and Pharmacokinetics of Novel Cannabidiol (CBD) Soft-gel Capsule Formulation (NW300EMCBD) in Healthy Subjects - Medical Cannabis Research Engine