The Pharmacokinetics, Safety, and Ease of Use of a Portable Metered-Dose Cannabis Inhaler
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ClinicalTrials.gov Identifier: NCT02729623 |
Recruitment Status : Unknown
Verified July 2016 by Kite Systems.
Recruitment status was: Enrolling by invitation
First Posted : April 6, 2016
Last Update Posted : July 25, 2016
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Condition or disease | Intervention/treatment | Phase |
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Healthy | Drug: Kite Systems cannaHALER cannabis Inhaler. | Phase 1 |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 12 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Single (Participant) |
Primary Purpose: | Treatment |
Official Title: | The Pharmacokinetics, Safety, and Ease of Use of a Portable Metered-Dose Cannabis Inhaler: A Phase 1a Study |
Study Start Date : | August 2016 |
Estimated Primary Completion Date : | December 2016 |
Estimated Study Completion Date : | August 2017 |
Arm | Intervention/treatment |
---|---|
Experimental: Single CannaHALER dose 10 ± 0.1 mg
Single dose 10 ± 0.1 mg of cannabis using the Kite Systems CannaHALER cannabis Inhaler device.
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Drug: Kite Systems cannaHALER cannabis Inhaler. |
Experimental: Single CannaHALER dose 15 ± 0.1 mg
Single dose 15 ± 0.1 mg of cannabis using the Kite Systems CannaHALER cannabis Inhaler device.
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Drug: Kite Systems cannaHALER cannabis Inhaler. |
Experimental: Single CannaHALER dose 20 ± 0.1 mg
Single dose 20 ± 0.1 mg of cannabis using the Kite Systems CannaHALER cannabis Inhaler device.
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Drug: Kite Systems cannaHALER cannabis Inhaler. |
Experimental: Single CannaHALER dose 25 ± 0.1 mg
Single dose 25 ± 0.1 mg of cannabis using the Kite Systems CannaHALER cannabis Inhaler device.
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Drug: Kite Systems cannaHALER cannabis Inhaler. |
- Δ9-tetrahydrocannabinol levels (THC) [ Time Frame: 30 Minutes ]
- Adverse event monitoring [ Time Frame: 4 hours ]
- Δ9 Carboxy-THC levels [ Time Frame: 30 Minutes ]
- Short Blessed cognitive Test [ Time Frame: 30 Minutes ]
- Blood pressure [ Time Frame: 120 Minutes ]
- Pulse rate [ Time Frame: 120 Minutes ]
- Oxygen saturation [ Time Frame: 120 Minutes ]

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 30 Years to 70 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- aged 30-70 years;
- healthy
- if applicable, negative pregnancy test (β human chorionic gonadotropin pregnancy test).
Exclusion Criteria:
- significant cardiac or pulmonary disease,
- history of a psychotic or anxiety disorder,
- pregnancy, pregnancy attempt or breastfeeding,
- presence of a neuropathic or non-neuropathic pain,
- low blood pressure, below 90 mm Hg (systolic)
- Diabetes is diagnosed,
- first degree family history of psychotic or anxiety disorder,
- history of drug addiction,
- history of drug misuse,
- using the following drugs: Rifampicin, Rifabutin, Carbamazepine, Phenobarbital, Primidone,
- using the following plants: Hypericum perforatum, troglitazone,
- Alcohol consumption up to 12 hours before the study,
- abnormal parameters such as Heart Rate above 100 BPM, Blood pressure, below 90 mm Hg (systolic), Saturation below 91 percent,
- Cannabis use up to 12 hours before the study,
- health condition which could affect or alter the experiment results,
- Volunteer has a legal guardian.
- Chronic use of drugs,
- age less than 30 or more than 70,
- a health condition that could affect the outcome of the trial or constitutes a risk factor for participation in the trial.
- The experiment will not include special populations such as pregnant women, children and without judgement.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02729623
Principal Investigator: | Ofir Ben-Ishay, MD. | Rambam Health Care Campus |
Responsible Party: | Kite Systems |
ClinicalTrials.gov Identifier: | NCT02729623 |
Other Study ID Numbers: |
cannaHALER-1A |
First Posted: | April 6, 2016 Key Record Dates |
Last Update Posted: | July 25, 2016 |
Last Verified: | July 2016 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Marijuana Abuse Substance-Related Disorders Chemically-Induced Disorders Mental Disorders |