Tolerability and Efficacy of CBD Extract for RLS Treatment

Phase 2Not Yet RecruitingNCT07224932

University of Colorado, Denver60 enrolled

Overview

This study plans to learn more about the safety and tolerability of high Cannabidiol (CBD) cannabis extract (BRC-002) for use in Idiopathic Restless Legs Syndrome. Symptoms and side effects experienced while taking the study drug will be tracked to determine if this medication is safe to use.

This randomized, placebo-controlled clinical trial will evaluate the safety, tolerability, and therapeutic effects of a high-CBD botanical extract in patients with idiopathic RLS. The study will examine changes in symptom severity, sleep quality, mood, and daily functioning to determine whether cannabinoid-based therapy offers a viable alternative or adjunctive treatment for RLS. Some inclusion/exclusion criteria are purposely omitted at this time to preserve scientific integrity. They will be included after the trial is complete.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

Conditions

Restless Leg Syndrome

Interventions

BRC-002DRUG

BRC-002 is a non-scheduled cannabidiol (CBD) formulation (\<0.3% THC). The cannabinoids in BRC-002 are naturally biosynthesized within the Cannabis sativa L. plant. BRC-002 is a high Cannabidiol Botanical extract (100 mg/mL).

PlacecboDRUG

Oral solution of mono-, di-, and triglycerides

Eligibility

Sex: ALLMin age: 18 YearsMax age: 79 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Male or female subjects between 18 and 79 years of age, inclusive. 2. Willing and able to give informed consent. 3. Idiopathic RLS, meeting all 4 International RLS Study Group diagnostic criteria. 4. Moderate or severe symptoms, defined as an IRLS score ≥ 15 at screening visit. 5. RLS medications unchanged for 4 weeks prior to baseline. 6. Must have a driver or available transportation (including provided Uber vouchers) to drive them to and from study visits and for other transportation needs during the treatment period. 7. Has a significant other, caregiver, or close acquaintance who knows the subject well and agrees to participate in the subject's neuropsychiatric assessment. 8. Agrees to not take more than 1 gram per day of acetaminophen. 9. Whereas applicable, agrees to utilize an effective method of contraception from screening through at least 4 weeks after the completion of study treatment. Exclusion Criteria: 1. Secondary RLS, such as Parkinson's disease or end-stage renal disease. 2. Present or past history of another severe sleep disorder. 3. Currently on night shift work schedule. 4. History or diagnosis of schizophrenia, bipolar or a psychotic disorder, severe depression, or any mental health illness that would compromise the safety of the participant. 5. Current suicidal ideation. 6. Severe cognitive impairment (e.g., Alzheimer's Disease, traumatic brain injury). 7. Uncontrolled hypertension. 8. Known or suspected allergy or hypersensitivity to cannabinoids or excipients used in the study drug formulation. 9. Pending legal action or workers compensation. 10. Cannabis use (THC) detectable at the screening/baseline visits. 11. History of drug or alcohol dependence. 12. Use of dopamine blockers, cocaine, or MAO-A inhibitors within 90 days of baseline. 13. Use of any drugs with known interactions with cannabinoids (e.g., tolcapone, clopidogrel, felbamate, warfarin, barbiturates, benzodiazepines, niacin, nicotinamide, isoniazid, ketoconazole, clobazam, valproate, mTOR inhibitors) within 90 days of baseline. 14. Unstable medical condition. 15. Clinically significant laboratory abnormalities. 16. Moderate or severe hepatic impairment. 17. Is pregnant, lactating, or has a positive pregnancy test result pre-dose. 18. Planned elective surgery during study participation.

Outcomes

Primary Outcomes

To examine the safety and tolerability of oral high CBD extract in idiopathic RLS assessed by frequency of adverse events which will be monitored by patient reported adverse events, vital signs, physical exam, and safety labs during study visits.

Participant reports measures the frequency of adverse events. This will be done with open-ended questions during patient visits and phone calls. Abnormal vital signs (BP, HR, RR) at patient visits measures the frequency of participants with adverse events. BP over 130/80 mmHg indicates worse outcomes. Lower scores indicate worse outcomes. HR ranges from 60 to 100 bpm; Scores outside this range indicates worse outcomes. RR ranges from 12-20 bpm. Scores outside this range indicated worse outcomes. A neurological exam and routine physical exam will be preformed to examine adverse events. Abnormal findings will constitute as an adverse event. Labs (serum CBC w/ diff, serum CMP, urinalysis) will measure frequency of adverse events. Abnormal CBC w/diff, CMP, and urinalysis values will be determined by lab ranges.

Time frame: Baseline, Visit 3, Visit 4, Visit 5

Secondary Outcomes

To examine the effect of BRC-002 on RLS symptoms assessed through changes from baseline in RLS-6 Severity Scale

The RLS-6 Severity Scale ranges from 0-60; increasing scores indicates a worse outcome.

Time frame: Baseline; Day 20

To examine the effect of BRC-002 on RLS symptoms assessed through changes from baseline in change from baseline in International Restless Legs Syndrome Study Group Rating Scale (IRLS)

The International Restless Legs Syndrome Study Group Rating Scale (IRLS) measures RLS symptoms. Scores range from 0 to 40, with higher scores indicating a worse outcome.

Time frame: Baseline; Day 20

To examine the effect of BRC-002 on RLS symptoms assessed through changes in sleep quality index (SQI) as measured by the SleepImage Ring

The SleepImage Recorder ring measures quality of sleep. Scores range from 0 to 100, with higher scores indicating a better outcome.

Central Contacts

Jacquelyn Bainbridge

CONTACT

303-810-4254 Jacci.Bainbridge@cuanschutz.edu

Data from ClinicalTrials.gov

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