Efficacy and Safety of GWP42003-P for Seizures Associated With Lennox-Gastaut Syndrome in Children and Adults

This study was a 1:1:1 randomized, double-blind, 14-week comparison of 2 dose levels (10
milligram [mg] per kilogram [kg] per day [mg/kg/day] and 20 mg/kg/day) of GWP42003-P versus
placebo. Participants who satisfied all inclusion and none of the exclusion criteria began a
28-day baseline observation period. The treatment period consisted of a 2-week titration
period followed by a 12-week maintenance period. The 20 mg/kg/day dose was recommended by the
Data Safety Monitoring Committee (DSMC) after assessment of safety and pharmacokinetic data
from Part A of study GWEP1332 (NCT02091206). The 10 mg/kg/day dose was defined as 50% of the
20 mg/kg/day dose. The first participant was not enrolled into this study until the DSMC had
reviewed the safety data from Part A of study GWEP1332.

Participants who satisfied all eligibility criteria were randomized at Day 1 to receive 10
mg/kg/day GWP42003-P, 20 mg/kg/day GWP42003-P, or placebo at a 1:1:1 ratio. Participants in
the placebo group were split into 2 equivalent cohorts; one half received 10 mg/kg/day dosing
volumes and one half received 20 mg/kg/day dosing volumes. The 2 placebo cohorts were pooled
for the analyses of efficacy. Participants titrated GWP42003-P to the 10 mg/kg/day or 20
mg/kg/day (or equivalent volume of placebo) dose over 7 and 11 days, respectively, and
remained at this dose for the 12-week maintenance period. Following the end of treatment (Day
99), participants were invited to continue to receive GWP42003-P in an open-label extension
(OLE) study under a separate protocol (GWEP1415; NCT02224573). All participants who did not
immediately enter the OLE study tapered investigational medicinal product (IMP) (10% per day
over 10 days). However, the taper period could be interrupted if the participant wished to
enter the OLE study within a 7-day timeframe. Participants who down-titrated IMP returned for
an end of taper period visit (Day 109). Participants who did not enter the OLE study or who
withdrew prematurely had a safety follow-up visit 28 days later (Day 137).

Key Inclusion Criteria:

- Participant and/or parent(s)/legal representatives were willing and able to give
informed assent/consent for participation in the study.

- Participant and his or her caregivers were willing and able (in the investigator's
opinion) to comply with all study requirements.

- Participant was male or female aged between 2 and 55 years (inclusive).

- Participant had a documented history of LGS. This included written documentation of
having met electroencephalogram (EEG) diagnostic criteria during the participant's
history and evidence of at least 1 type of generalized seizure, including drop
seizures (atonic, tonic, tonic-clonic or myoclonic) for at least 6 months.

- Participant had a history of slow (<3.0 hertz [Hz]) spike-and-wave pattern in an EEG
prior to the enrollment into the baseline period.

- Participant had at least 2 drop seizures each week during the first 28 days of the
baseline period.

- Participant was refractory; that is having documented failures on more than 1
antiepileptic drug (AED).

- Participant was taking 1 or more AEDs at a dose which had been stable for at least 4
weeks prior to screening.

- All medications or interventions for epilepsy (including ketogenic diet and vagus
nerve stimulation [VNS]) were stable for 4 weeks prior to screening and the
participant was willing to maintain a stable regimen throughout the study. The
ketogenic diet and VNS treatments were not counted as an AED.

- Participant and/or parent(s)/legal representatives were willing to allow his or her
primary care practitioner and consultant to be notified of participation in the study.

- Participant completed his or her interactive voice response (IVRS) telephone diary on
at least 25 days of the baseline period.

Key Exclusion Criteria:

- Etiology of participant's seizures was a progressive neurologic disease. Participants
with tuberous sclerosis were not excluded from study participation, unless there was a
progressive tumor.

- Participant had an anoxic episode requiring resuscitation within 6 months of
screening.

- Participant had clinically significant unstable medical conditions other than
epilepsy.

- Participant had clinically relevant symptoms or a clinically significant illness in
the 4 weeks prior to screening or randomization, other than epilepsy.

- Participant had a history or presence of alcohol or substance abuse within the last 2
years prior to the study or daily consumption of 5 or more alcohol-containing
beverages.

- Participant was currently using or had in the past used recreational or medicinal
cannabis, or synthetic cannabinoid-based medications (including Sativex®) within the 3
months prior to study entry and was unwilling to abstain for the duration of the
study.

- Participant had a history of symptoms (for example, dizziness, light-headedness,
blurred vision, palpitations, weakness, syncope) related to a drop in blood pressure
due to postural changes.

- Participant had any known or suspected hypersensitivity to cannabinoids or any of the
excipients of the IMP, such as sesame oil.

- Female participant was of child bearing potential or male participant's partner was of
child bearing potential; unless willing to ensure that they or their partner used a
highly effective method of contraception for the duration of the study and for 3
months thereafter.

- Female participant was pregnant (positive pregnancy test), lactating or planning
pregnancy during the course of the study and for 3 months thereafter.

- Participant had been part of a clinical study involving another IMP in the previous 6
months.

- Patient had significantly impaired hepatic function at screening (Day -28) or
randomization (Day 1), defined as any of the following: alanine aminotransferase (ALT)
or aspartate aminotransferase (AST) > 5 × upper limit of normal (ULN); ALT or AST > 3
× ULN and total bilirubin > 2 × ULN or international normalized ratio (INR) > 1.5; ALT
or AST > 3 × ULN with the presence of fatigue, nausea, vomiting, right upper quadrant
pain or tenderness, fever, rash, and/or eosinophilia (>5%). This criterion could only
be confirmed once the laboratory results were available; participants randomized into
the study who were later found not to meet this criterion were withdrawn from the
study.

- Any history of suicidal behavior or any suicidal ideation of type 4 or 5 on the
Columbia Suicide Severity Rating Scale in the last month or at screening.

- Participant was unwilling to abstain from donation of blood during the study.

- Participant planned to travel outside his or her country of residence during the
study.

- Participant had previously randomized into the study.

- Participant was taking more than 4 concurrent AEDs.

- Participant had taken corticotropins in the 6 months prior to screening.

- Participant was currently taking long-term systemic steroids (excluding inhaled
medication for asthma treatment) or any other daily medication known to exacerbate
epilepsy. An exception was made of prophylactic medication, for example, idiopathic
nephrotic syndrome or asthma.

- Participant was taking felbamate, and he or she had been taking it for less than 1
year prior to screening.