Back to resultsA Study of the Safety and Tolerability of GWP42006 in Healthy Subjects
Primary Purpose
Epilepsy
Status
Completed
Phase
Phase 1
Locations
United Kingdom
Study Type
Interventional
Intervention
Placebo
GWP42006
Sponsored by
About this trial
This is an interventional treatment trial for Epilepsy focused on measuring Safety, Tolerability, Assessment of potential adverse events, Assessment of potential laboratory abnormalities
Eligibility Criteria
Inclusion Criteria:
- Healthy females of non-childbearing potential or healthy males
- Age 18 to 65 years, inclusive
- Body mass index of 18 to 30 kg/m2 inclusive or, if outside the range, considered not clinically significant by the investigator
- Must have no clinically significant abnormal findings on physical examination, vital signs, electrocardiogram, medical history, or clinical laboratory results during screening or Day -1 (admission)
- Must be willing and able to communicate and participate in the whole study
- Must provide written informed consent
- Must be willing to allow his or her primary care practitioner and consultant, if appropriate, to be notified of participation in the study
- Must agree to use an adequate method of contraception: Two or more of the following methods are acceptable and must include at least one barrier method:
- Surgical sterilisation (i.e. bilateral tubal ligation, hysterectomy for female partners; vasectomy for males)
- Placement of an intrauterine device or intrauterine system
- Hormonal contraception (implantable, patch, oral)
- Barrier methods (for male subjects, this must be a condom; for female subjects, either their partner's use of a condom or the subject's use of an occlusive cap [diaphragm or cervical/vault caps] with spermicidal foam/gel/film/cream/suppository).
- Alternatively, true abstinence is acceptable when it is in line with the subject's preferred and usual lifestyle.
Exclusion Criteria:
- Participation in a clinical research study/receiving an Investigational Medicinal Product within the 3 months prior to screening
- Subjects who are study site employees, or immediate family members of a study site or sponsor employee
- Subjects who have previously been randomised in this study
- History of any drug or alcohol abuse in the past 2 years, or current habituation to any medications or illegal drugs
- Regular alcohol consumption in males >21 units per week and females >14 units per week (1 unit = 0.5 pint beer, 25 mL of 40% spirit or a 125 mL glass of wine)
- Tobacco product use in the previous 6 months. A breath carbon monoxide reading of greater than 10 ppm at screening
- Subjects who do not have suitable veins for multiple venepunctures/cannulation as assessed by the investigator at screening
- Clinically significant abnormal clinical chemistry, haematology or urinalysis as judged by the investigator
- Positive drugs of abuse test result
- Positive hepatitis B surface antigen, hepatitis C virus antibody or human immunodeficiency virus-1 and -2 results
- History of clinically relevant physical abnormalities, medical conditions or clinical laboratory test results e.g. cardiovascular, renal, hepatic, pulmonary, haematological, endocrinological, neurological, psychiatric, chronic respiratory or gastrointestinal disease as judged by the investigator
- Clinically relevant symptoms or a clinically significant illness in the 4 weeks prior to screening
- Known cardiovascular condition or history of a cardiovascular condition or clinically relevant abnormalities in the 12-lead electrocardiogram measured at screening
- Subject has a postural drop of 20 mmHg or more in systolic blood pressure at screening, with features of postural hypotension, in the opinion of the investigator
- Concurrent cardiovascular conditions, which will, in the investigators opinion, interfere with the ability to read their electrocardiograms
- Current use or past use of recreational or medicinal cannabis, or cannabinoid based medications (including Sativex) within the 3 months prior to study entry and is unwilling to abstain for the duration for the study
- Serious adverse reaction or serious hypersensitivity to any drug or the formulation excipients (e.g. cannabinoids, sesame oil)
- Presence or history of clinically significant allergy requiring treatment as judged by the investigator. Hayfever is allowed unless it is active
- Donation or loss of greater than 500 mL of blood within the previous 3 months
- Unwilling to abstain from donation of blood during the planned study
- Subjects who are taking, or have taken, any prescribed or over-the-counter drug (other than 4 g per day paracetamol and hormone replacement therapy) or herbal remedies in the 14 days before Investigational Medicinal Product administration
- Travel outside the country of residence planned during the study
- Failure to satisfy the investigator of fitness to participate for any other reason
Sites / Locations
- Quotient Clinical
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Arm 7
Arm 8
Arm 9
Arm 10
Arm Type
Experimental
Placebo Comparator
Experimental
Placebo Comparator
Experimental
Placebo Comparator
Experimental
Placebo Comparator
Experimental
Placebo Comparator
Arm Label
Group/dose level 1a
Group/dose level 1b
Group/dose level 2a
Group/dose level 2b
Group/dose level 3a
Group/dose level 3b
Group/dose level 4a
Group/dose level 4b
GWP42006 1, 2, or 3 times daily
Placebo 1, 2, or 3 times daily
Arm Description
25 mg GWP42006 oral solution. As a safety precaution, subjects will be split into two sub-groups for sentinel dosing. On the first day of dosing , only two subjects will be dosed (randomisation schedule designed so that one placebo one active will be dosed on first day). Following a review of the safety data for the first set of subjects, the remaining subjects will be dosed.
Matching placebo for Group/dose level 1a. As a safety precaution, subjects will be split into two sub-groups for sentinel dosing. On the first day of dosing , only two subjects will be dosed (randomisation schedule designed so that one placebo one active will be dosed on first day). Following a review of the safety data for the first set of subjects, the remaining subjects will be dosed.
75 mg GWP42006 oral solution. As a safety precaution, subjects will be split into two sub-groups for sentinel dosing. On the first day of dosing , only two subjects will be dosed (randomisation schedule designed so that one placebo one active will be dosed on first day). Following a review of the safety data for the first set of subjects, the remaining subjects will be dosed.
Matching placebo for Group/dose level 2a. As a safety precaution, subjects will be split into two sub-groups for sentinel dosing. On the first day of dosing , only two subjects will be dosed (randomisation schedule designed so that one placebo one active will be dosed on first day). Following a review of the safety data for the first set of subjects, the remaining subjects will be dosed.
200 mg GWP42006 oral solution (single dose) followed by an intravenous administration of 5 mg GWP42006 after the oral dose
Matching placebo for Group/dose level 3a
400 mg GWP42006 oral solution
Matching placebo for Group/dose level 4a
Subjects will receive the selected dose of GWP42006 once, twice or three times daily (the number of daily doses and actual dose will be decided upon based on results from Part 1 of the study) for a total of 5 days, with the final dose given on the morning of Day 5.
Subjects will receive placebo once, twice or three times daily (the number of daily doses and actual dose will be decided upon based on results from Part 1 of the study) for a total of 5 days, with the final dose given on the morning of Day 5.
Outcomes
Primary Outcome Measures
The incidence of adverse events as measure of subject safety
The number of subjects who experienced an adverse event during each arm of the study is presented.
Secondary Outcome Measures
To determine the plasma concentration time curves for GWP42006, 7-hydroxy-GWP42006 and 6-hydroxy-GWP42006 compounds, following escalating single doses and multiple doses of pure GWP42006.
For oral dosing, the pre-dose blood sample was taken ≤1 h before dosing.
For intravenous dosing, the pre-dose sample was taken immediately before the intravenous bolus infusion.
0 to 1 h post-dose samples were taken within ± 2 min of the nominal post-dose sampling time (the 0.04 and 0.08 h pharmacokinetic samples taken post-intravenous dosing only were taken at the middle and the end of the intravenous bolus infusion).
>1 to 12 h post-dose samples were taken within ± 10 min of the nominal post-dose sampling time.
>12 h post-dose samples were taken within ± 30 min of the nominal post-dose sampling time if subjects were resident in the clinic.
The following pharmacokinetic parameters were investigated: Tmax, Area Under the plasma concentration Curve (AUC)(0-inf), AUC(0-t), T1/2el, F, AUC(0-tau) and Kel.
To investigate cognitive function following single ascending and multiples doses of GWP42006
A cognitive assessment was carried using the Fepsy battery. The following tests were carried out: auditory reaction times (left and right), recognition simultaneously (6 words, 4 figures), visual reaction task (white square, left and right), computerised visual searching task (24 small figures), finger tapping task, recognition serially (6 words, 4 figures) and binary choice task (random).
To investigate gene expression following multiple doses of GWP42006
Analysis of gene expression was carried out for subjects participating in the multiple dose phase of the study.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01918735
Brief Title
A Study of the Safety and Tolerability of GWP42006 in Healthy Subjects
Official Title
A Randomised, Double-Blind, Placebo-Controlled, Dose Escalation, Safety, Tolerability and Pharmacokinetics Study of Single Ascending and Multiple Doses of GWP42006 in Healthy Volunteers
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
August 2013 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Jazz Pharmaceuticals
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The primary objective of this study is to evaluate the safety and tolerability of single ascending (increasing) and multiple doses of GWP42006 compared with placebo.
Detailed Description
This is a single-centre, randomised, double-blind, placebo-controlled, parallel group dose escalation, safety, tolerability and pharmacokinetic (PK) study of single escalating and multiple doses of GWP42006 in healthy volunteers. The study consists of 5 single dosing occasions, and a five day repeated dose period.
Part 1 Single Dosing:
Four parallel groups of 11 subjects will participate in the oral single dosing, dose escalation study phase. In each group, subjects will be randomly assigned so that eight subjects receive active and three subjects receive placebo. It is planned for Groups 1 and 2, that a staggered 'sentinel' dose design will be used, with two sub-groups:
The first will comprise of one placebo and one active subject.
In the second, seven subjects will receive active and two will receive placebo after a review of the 24 h post-dose safety data of the first group.
Sentinel subject dosing will be performed in higher-dose groups if there is no measurable plasma GWP42006 in Group 1 or 2.
One group within the single dosing part (Group 3/dose level 3) will then receive an intravenous administration of 5 mg GWP42006 to allow assessment of bioavailability. There will be a minimum of seven days between doses.
Up to three further groups may be added for further evaluations, e.g. to assess additional dose levels or food effect. The need for additional groups will be based on a review of the safety, tolerability and PK data by the safety advisory committee.
Dose Escalation:
The planned dose levels are 25 mg (Group 1/dose level 1), 75 mg (Group 2/dose level 2), 200 mg (Group 3/dose level 3) and 400 mg (Group 4/dose level 4), with a maximum dose of 800 mg. Administration of each successive dose will be dependent on safety, tolerability and PK data of previous doses.
Part 2 Multiple Dosing:
The doses and dose regimens assessed in Part 2 will be selected based upon the safety, and PK data from Part 1 of the study.
It is planned that one group of 11 subjects will participate in the multiple dose phase, and subjects will be randomly assigned so that eight subjects receive active and three receive matching placebo. Each subject will receive the selected dose of GWP42006 or placebo once, twice or three times daily for a total of five days, with the final dose administered on the morning of Day 5.
Up to two further groups may be added for further evaluations, e.g. to assess a different dose level or a different dosing frequency. As for single dosing, the decision to include further groups will be taken based on safety, tolerability and PK data. All further groups would be added on blinded information.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Epilepsy
Keywords
Safety, Tolerability, Assessment of potential adverse events, Assessment of potential laboratory abnormalities
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
66 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group/dose level 1a
Arm Type
Experimental
Arm Description
25 mg GWP42006 oral solution. As a safety precaution, subjects will be split into two sub-groups for sentinel dosing. On the first day of dosing , only two subjects will be dosed (randomisation schedule designed so that one placebo one active will be dosed on first day). Following a review of the safety data for the first set of subjects, the remaining subjects will be dosed.
Arm Title
Group/dose level 1b
Arm Type
Placebo Comparator
Arm Description
Matching placebo for Group/dose level 1a. As a safety precaution, subjects will be split into two sub-groups for sentinel dosing. On the first day of dosing , only two subjects will be dosed (randomisation schedule designed so that one placebo one active will be dosed on first day). Following a review of the safety data for the first set of subjects, the remaining subjects will be dosed.
Arm Title
Group/dose level 2a
Arm Type
Experimental
Arm Description
75 mg GWP42006 oral solution. As a safety precaution, subjects will be split into two sub-groups for sentinel dosing. On the first day of dosing , only two subjects will be dosed (randomisation schedule designed so that one placebo one active will be dosed on first day). Following a review of the safety data for the first set of subjects, the remaining subjects will be dosed.
Arm Title
Group/dose level 2b
Arm Type
Placebo Comparator
Arm Description
Matching placebo for Group/dose level 2a. As a safety precaution, subjects will be split into two sub-groups for sentinel dosing. On the first day of dosing , only two subjects will be dosed (randomisation schedule designed so that one placebo one active will be dosed on first day). Following a review of the safety data for the first set of subjects, the remaining subjects will be dosed.
Arm Title
Group/dose level 3a
Arm Type
Experimental
Arm Description
200 mg GWP42006 oral solution (single dose) followed by an intravenous administration of 5 mg GWP42006 after the oral dose
Arm Title
Group/dose level 3b
Arm Type
Placebo Comparator
Arm Description
Matching placebo for Group/dose level 3a
Arm Title
Group/dose level 4a
Arm Type
Experimental
Arm Description
400 mg GWP42006 oral solution
Arm Title
Group/dose level 4b
Arm Type
Placebo Comparator
Arm Description
Matching placebo for Group/dose level 4a
Arm Title
GWP42006 1, 2, or 3 times daily
Arm Type
Experimental
Arm Description
Subjects will receive the selected dose of GWP42006 once, twice or three times daily (the number of daily doses and actual dose will be decided upon based on results from Part 1 of the study) for a total of 5 days, with the final dose given on the morning of Day 5.
Arm Title
Placebo 1, 2, or 3 times daily
Arm Type
Placebo Comparator
Arm Description
Subjects will receive placebo once, twice or three times daily (the number of daily doses and actual dose will be decided upon based on results from Part 1 of the study) for a total of 5 days, with the final dose given on the morning of Day 5.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Placebo control
Intervention Description
Placebo control matched to the oral or intravenous experimental comparator drug
Intervention Type
Drug
Intervention Name(s)
GWP42006
Intervention Description
Oral administration of 25 (Group/dose level 1a and 1b), 75 (Group/dose level 2a and 2b), 200 (Group/dose level 3a and 3b) and 400 mg GWP42006 (Group/dose level 4a and 4b), provided as 50 mg/mL GWP42006 solution in sesame oil containing flavourings and sweetener, for dilution on the day of dosing, as required.
Additional intravenous administration of 5 mg GWP42006 and 10 mL Solutol HS 15 solution to Group/dose level 3a and 3b subjects.
Primary Outcome Measure Information:
Title
The incidence of adverse events as measure of subject safety
Description
The number of subjects who experienced an adverse event during each arm of the study is presented.
Time Frame
Day 0 - Day 10
Secondary Outcome Measure Information:
Title
To determine the plasma concentration time curves for GWP42006, 7-hydroxy-GWP42006 and 6-hydroxy-GWP42006 compounds, following escalating single doses and multiple doses of pure GWP42006.
Description
For oral dosing, the pre-dose blood sample was taken ≤1 h before dosing.
For intravenous dosing, the pre-dose sample was taken immediately before the intravenous bolus infusion.
0 to 1 h post-dose samples were taken within ± 2 min of the nominal post-dose sampling time (the 0.04 and 0.08 h pharmacokinetic samples taken post-intravenous dosing only were taken at the middle and the end of the intravenous bolus infusion).
>1 to 12 h post-dose samples were taken within ± 10 min of the nominal post-dose sampling time.
>12 h post-dose samples were taken within ± 30 min of the nominal post-dose sampling time if subjects were resident in the clinic.
The following pharmacokinetic parameters were investigated: Tmax, Area Under the plasma concentration Curve (AUC)(0-inf), AUC(0-t), T1/2el, F, AUC(0-tau) and Kel.
Time Frame
Pre-dose then 0, 0.04, 0.08, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 24, 36, 48 h post-dose
Title
To investigate cognitive function following single ascending and multiples doses of GWP42006
Description
A cognitive assessment was carried using the Fepsy battery. The following tests were carried out: auditory reaction times (left and right), recognition simultaneously (6 words, 4 figures), visual reaction task (white square, left and right), computerised visual searching task (24 small figures), finger tapping task, recognition serially (6 words, 4 figures) and binary choice task (random).
Time Frame
Admission (Day -1) and 2 h post-dose
Title
To investigate gene expression following multiple doses of GWP42006
Description
Analysis of gene expression was carried out for subjects participating in the multiple dose phase of the study.
Time Frame
Pre-dose on multiple dose Days 1-4 then 2 h post-dose on multiple dose Day 5
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Healthy females of non-childbearing potential or healthy males
Age 18 to 65 years, inclusive
Body mass index of 18 to 30 kg/m2 inclusive or, if outside the range, considered not clinically significant by the investigator
Must have no clinically significant abnormal findings on physical examination, vital signs, electrocardiogram, medical history, or clinical laboratory results during screening or Day -1 (admission)
Must be willing and able to communicate and participate in the whole study
Must provide written informed consent
Must be willing to allow his or her primary care practitioner and consultant, if appropriate, to be notified of participation in the study
Must agree to use an adequate method of contraception: Two or more of the following methods are acceptable and must include at least one barrier method:
Surgical sterilisation (i.e. bilateral tubal ligation, hysterectomy for female partners; vasectomy for males)
Placement of an intrauterine device or intrauterine system
Hormonal contraception (implantable, patch, oral)
Barrier methods (for male subjects, this must be a condom; for female subjects, either their partner's use of a condom or the subject's use of an occlusive cap [diaphragm or cervical/vault caps] with spermicidal foam/gel/film/cream/suppository).
Alternatively, true abstinence is acceptable when it is in line with the subject's preferred and usual lifestyle.
Exclusion Criteria:
Participation in a clinical research study/receiving an Investigational Medicinal Product within the 3 months prior to screening
Subjects who are study site employees, or immediate family members of a study site or sponsor employee
Subjects who have previously been randomised in this study
History of any drug or alcohol abuse in the past 2 years, or current habituation to any medications or illegal drugs
Regular alcohol consumption in males >21 units per week and females >14 units per week (1 unit = 0.5 pint beer, 25 mL of 40% spirit or a 125 mL glass of wine)
Tobacco product use in the previous 6 months. A breath carbon monoxide reading of greater than 10 ppm at screening
Subjects who do not have suitable veins for multiple venepunctures/cannulation as assessed by the investigator at screening
Clinically significant abnormal clinical chemistry, haematology or urinalysis as judged by the investigator
Positive drugs of abuse test result
Positive hepatitis B surface antigen, hepatitis C virus antibody or human immunodeficiency virus-1 and -2 results
History of clinically relevant physical abnormalities, medical conditions or clinical laboratory test results e.g. cardiovascular, renal, hepatic, pulmonary, haematological, endocrinological, neurological, psychiatric, chronic respiratory or gastrointestinal disease as judged by the investigator
Clinically relevant symptoms or a clinically significant illness in the 4 weeks prior to screening
Known cardiovascular condition or history of a cardiovascular condition or clinically relevant abnormalities in the 12-lead electrocardiogram measured at screening
Subject has a postural drop of 20 mmHg or more in systolic blood pressure at screening, with features of postural hypotension, in the opinion of the investigator
Concurrent cardiovascular conditions, which will, in the investigators opinion, interfere with the ability to read their electrocardiograms
Current use or past use of recreational or medicinal cannabis, or cannabinoid based medications (including Sativex) within the 3 months prior to study entry and is unwilling to abstain for the duration for the study
Serious adverse reaction or serious hypersensitivity to any drug or the formulation excipients (e.g. cannabinoids, sesame oil)
Presence or history of clinically significant allergy requiring treatment as judged by the investigator. Hayfever is allowed unless it is active
Donation or loss of greater than 500 mL of blood within the previous 3 months
Unwilling to abstain from donation of blood during the planned study
Subjects who are taking, or have taken, any prescribed or over-the-counter drug (other than 4 g per day paracetamol and hormone replacement therapy) or herbal remedies in the 14 days before Investigational Medicinal Product administration
Travel outside the country of residence planned during the study
Failure to satisfy the investigator of fitness to participate for any other reason
Facility Information:
Facility Name
Quotient Clinical
City
Nottingham
ZIP/Postal Code
NG11 6JS
Country
United Kingdom
12. IPD Sharing Statement
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A Study of the Safety and Tolerability of GWP42006 in Healthy Subjects
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