The safety, tolerability, and effectiveness of PTL-101, an oral cannabidiol formulation, in pediatric intractable epilepsy: A phase II, open-label, single-center study

Alexis Mitelpunkt*, Uri Kramer, Moran Hausman Kedem, Efrat Zilbershot Fink, Rotem Orbach, Veronika Chernuha, Aviva Fattal-Valevski, Lisa Deutsch, Daphna Heffetz, Hagit Sacks

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

Introduction: Several works have reported on the antiepileptic impact of cannabis-based preparations in patients with treatment-resistant epilepsy (TRE). However, current formulations suffer from low bioavailability and side effects. PTL-101, an oral formulation containing highly purified cannabidiol (CBD) embedded in seamless gelatin matrix beadlets was designed to enhance bioavailability and maintain a constant gastrointestinal transit time. Methods: This phase II, prospective study was open to pediatric patients with TRE on stable antiepileptic drugs' (AEDs) doses, who experienced ≥ 4 seizures within four weeks of enrolment and with a history of ≥ 4 AEDs failing to provide seizure control. Following a 4-week observation period, patients began a 2-week dose-titration phase (up to ≤ 25 mg/kg or 450 mg, the lower of the two), followed by a 10-week maintenance treatment period. Caregivers recorded seizure frequency, type, and severity and ranked their global impressions after 7 and 12 weeks of treatment. Responders were those showing a ≥ 50% reduction from baseline monthly seizure frequency. Safety assessments monitored vital signs, adverse effects, physical and neurological exams, and laboratory tests. Results: Sixteen patients (age: 9.1 ± 3.4) enrolled in the study; 11 completed the full treatment program. The average maintenance dose was 13.6 ± 4.2 mg/kg. Patient adherence to treatment regimens was 96.3 ± 9.9%. By the end of the treatment period, 81.9% and 73.4 ± 24.6% (p < 0.05) reductions from baseline median seizure count and monthly seizure frequency, respectively, were recorded. Responders' rate was 56%; two patients became fully seizure-free. By study end, 8 (73%) caregivers reported an improved/very much improved condition, and 9 (82%) reported reduced/very much reduced seizure severity. Most commonly reported treatment-related adverse effects were sleep disturbance/insomnia, (4 (25.0%) patients), followed by somnolence, increased seizure frequency, and restlessness (3 patients each (18.8%)). None were serious or severe, and all resolved. Conclusions: PTL-101 was safe and tolerable for use and demonstrated a potent seizure-reducing effect among pediatric patients with TRE.

Original languageEnglish
Pages (from-to)233-237
Number of pages5
JournalEpilepsy and Behavior
Volume98
DOIs
StatePublished - Sep 2019

Funding

FundersFunder number
PSW Ltd
PhytoTech Therapeutics Ltd

    Keywords

    • Cannabidiol
    • Cannabinoids
    • Clinical study
    • Intractable epilepsy
    • Oral drug delivery
    • Pediatric

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