Investigation of the Efficacy and Safety of CHI-921 in Insomnia.

NCT ID: NCT03984604

Last Updated: 2020-10-05

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 21 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-03-21
• Study Completion Date: 2020-06-17

Brief Summary

Insomnia is a disorder where people are having trouble sleeping and can include difficulty falling asleep, staying asleep and waking up too early, as well as having unrefreshing sleep. CHI-921 is a cannabis extract in sunflower oil produced as a treatment for insomnia. This trial is designed to evaluate the efficacy and safety of CHI-921 on people with insomnia.

Detailed Description

The study is designed to:

1. Evaluate the patient-reported sleep latency and patient-reported wake after sleep onset after 3 weeks per treatment dose with CHI-921 compared to placebo.

2. To evaluate the effects of CHI-921 compared to placebo on PSG sleep architecture.

3. To evaluate the effects of CHI-921 compared to placebo on Patient Global Impression of change.

4. To evaluate the daytime residual effects that may be associated with CHI-921 as compared to placebo during the double-blind treatment period using patient's morning and evening questionnaire, Clinical Global Impression of change, Insomnia Severity Index, Pittsburgh Sleep Quality Index, Epworth Sleepiness Scale as well as the Rey Auditory Verbal Learning Test and Digit Symbol Substitution psychometric tests.

5. To assess the effect on sleep of abruptly discontinuing CHI-921 compared to placebo (during run-out period).

6. To evaluate the clinical safety and tolerability of CHI-921 compared to placebo.

7. Evaluation of the accuracy of sleep data obtained by actigraphy as compared to traditional PSG.

Conditions

Insomnia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

CHI-921

During the double-blind treatment period (9 weeks), subjects will take 0.5 mL of their randomized treatment (CHI-921) for 3 weeks, followed by another 3 weeks of treatment at 1.0 mL for and another 3 weeks of treatment at 2.0 mL.

Group Type: ACTIVE_COMPARATOR

CHI-921

Intervention Type: DRUG

a standardized cannabis extract in sunflower oil administered in oral liquid (oil) form

Placebo

During the double-blind treatment period (9 weeks), subjects will take 0.5 mL of their randomized treatment (placebo) for 3 weeks, followed by another 3 weeks of placebo treatment at 1.0 mL for and another 3 weeks of placebo treatment at 2.0 mL.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Placebo is a vehicle oil will match CHI-921

Interventions

CHI-921

a standardized cannabis extract in sunflower oil administered in oral liquid (oil) form

Intervention Type: DRUG

Placebo

Placebo is a vehicle oil will match CHI-921

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Male or female subjects 25 to 70 years of age, inclusive

2. Willing and able to give informed consent for study participation

3. Each patient must have insomnia disorder based on criteria (ICSD-3 or DSM-5) with predominant complaints of difficulty in initiating or maintaining sleep for at least three months preceding the study visit and having clinically significant distress or impairment in social occupational or other important areas of functioning

4. Normal vital signs as follows:

• Sitting systolic blood pressure (SBP) between 90 and 140 mmHg, inclusive
• Sitting diastolic blood pressure (DBP) between 55 and 90 mmHg, inclusive
• Pulse rate between 50 and 100 bpm inclusive

5. Willing to comply with all study requirements and procedures for the duration of the clinical study

6. Willing to comply with the study restrictions including:

• Adherence to concomitant drug washout requirements, as applicable, for the duration of the clinical study
• Willing to abstain from alcohol for the duration of the clinical study
• Willing to abstain from caffeine 10 hours before each recording
• If a smoker, willing to abstain from smoking at night from approximately 10 pm to 8 am for the duration of the clinical study

7. Female subjects who:

• Are postmenopausal, with amenorrhea for at least 1 year before the screening visit,
• Are surgically sterile, OR
• If of childbearing potential agree to practice effective double barrier methods of contraception, from the time of the signing of informed consent through the last dose of study drug and for 30 days after dosing stops (1 ovulatory cycle), or agree to completely abstain from intercourse
• Males with female partners of childbearing potential are also expected to practice effective barrier methods of contraception from the time of signing informed consent through the last dose of study drug and for 30 days after dosing stops.

8. Self-reported bedtime between 9 pm and midnight on 4-7 nights per week

9. Based on the PSG recordings during the screening nights (V2; SN1 and SN2), one of the following criteria must be present:

1. Mean WASO calculated on SN1 and SN2 > 30 min or

2. Mean LPS: calculated on SN1 and SN2 > 30 min

Exclusion Criteria

1. Body mass index > 32 calculated from patient's height (m) and weight (kg); weight (kg)/square height (m²)

2. Presence of a sleep disorder (for sleep apnea syndrome, an apnea-hypopnea index > 15 per hour of sleep on the first screening night will be used as an exclusion criterion; for periodic limb movement disorder, an index of periodic limb movements during sleep associated with an arousal > 10 per hour of sleep on the first screening night will be used as an exclusion criterion)

3. Patients with a history of epilepsy or seizures (not including benign neonatal and childhood convulsions)

4. Serious head injury or stroke within the past year

5. Any evidence of psychiatric disorder (including Beck Depression Inventory [BDI] ≥ 20) and/or history of psychosis excluding insomnia

6. Evidence of any clinically significant, severe or unstable, acute or chronically progressive medical or surgical disorder (including planned medical procedures that may impact sleep), or any condition that may interfere with the absorption, metabolism, distribution, or excretion of the study drug, or may affect patient safety

7. Clinically significant and abnormal electrocardiogram (ECG; including QTc ≥ 450 ms for males, 460 ms for females) or patients with a history of cardiovascular disease including poorly controlled hypertension, ischaemic heart disease, arrhythmia, or severe heart failure

8. Positive qualitative urine drug screen (opiates, cocaine, amphetamine, cannabinoids, barbiturates, phencyclidine, benzodiazepines, methadone, propoxyphene), at screening

9. Use of any substance with psychotropic effects or properties known to affect sleep/wake, including neuroleptics, morphine/opioid derivatives, antihistamines, stimulants antidepressants, clonidine, within one week or five half-lives (whichever is longer) prior to screening

10. Use of any over-the-counter sleep medications including tryptophan, valerian root (Valeriana officinalis), kava (Piper methysticum Forst), melatonin, St John's Wort (Hypericum perforatum), Alluna (herbal sleep supplement with valerian root), and hemp within 1 week or 5 half-lives (whichever is longer) prior to screening

11. Consumption of xanthine-containing beverages (i.e., tea, coffee, or cola) of more than 5 cups or glasses per day

12. Participation in any other trial within 30 days before the screening visit

13. Night shift workers (during the 12 months prior to the study and during the study)

14. Individuals who nap 3 or more times per week over the preceding month

15. Individuals having to travel across more than 3 time zones in the month prior to screening or individuals who plan on travelling outside of their country of residence at any time during the study

17. Women who are pregnant, are planning to become pregnant, or are breastfeeding

18. Individuals may be excluded from participating in the study based on the investigator's professional judgement

• Minimum Eligible Age: 25 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Galenova Inc

OTHER

Sponsor Role: collaborator

Algorithme Pharma Inc

INDUSTRY

Sponsor Role: collaborator

Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal

OTHER

Sponsor Role: collaborator

McGill University Health Centre/Research Institute of the McGill University Health Centre

OTHER

Sponsor Role: collaborator

Centre hospitalier de l'Université de Montréal (CHUM)

OTHER

Sponsor Role: collaborator

Canopy Growth Corporation

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Dr M Ware, MD

Role: STUDY_DIRECTOR

Canopy Growth Corporation

Locations

Algorithme Pharma Inc.

Montreal, Quebec, Canada

Countries

Canada

Other Identifiers

H2017-01

Identifier Type: -

Identifier Source: org_study_id