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Abstract Details

Tuberous Sclerosis Complex (TSC)–Associated Neuropsychiatric Disorders (TAND) Outcomes Following Adjunctive Cannabidiol (CBD) Treatment: 6-Month Intermediate Analysis of the EpiCom Trial
Epilepsy/Clinical Neurophysiology (EEG)
S5 - Clinical Epilepsy (1:48 PM-2:00 PM)
005

This prespecified 6-month analysis of the ongoing EpiCom phase 3b/4 study (NCT05864846) investigated TAND outcomes after adjunctive cannabidiol (CBD; Epidiolex® [US]/Epidyolex® [EU], 100 mg/mL oral solution) initiation in participants with TSC-associated seizures.

TAND reduce quality of life in a majority of people with TSC, yet treatment options remain limited. Anecdotal evidence suggests some neuropsychiatric benefits of CBD.

Participants with TSC and moderate/severe behavioral challenges received CBD ≤25 mg/kg/day plus standard of care (SOC) for 26 weeks, followed by CBD+SOC or SOC alone for ≤26 additional weeks. Most problematic behavior (MPB), TAND Self-Report Quantified Checklist (TAND-SQ), Aberrant Behavior Checklist (ABC), Caregiver Global Impression of Severity (CareGI-S), and Clinician Global Impression of Severity (CGI-S) scales were assessed at baseline, Week (W) 13, and W26.

Of 79 participants enrolled at 6 months, 62 had ≥1 postbaseline assessment. At baseline, median (range) age was 16.0 (3–42) years; 2.0 (1–6) antiseizure medications were used and median MPB numerical rating scale (NRS) value was 9.0 of 10, suggesting severe TAND. At W26, median change from baseline in MPB NRS was −2.0. Greatest changes among TAND-SQ clusters were eat/sleep (−2.0) and overactive/impulsive (−1.3); among ABC subscales, irritability (−8.0) and hyperactive noncompliance (−7.0). Compared with baseline, fewer caregivers and clinicians rated behavioral problems as severe/very severe post-treatment at W13 and W26, respectively (CareGI-S severe: 38% vs 14% and 13%; very severe: 18% vs 4% and 13%; CGI-S severe: 47% vs 10% and 0%; very severe: 10% vs 0% and 0%). Treatment-emergent adverse events occurred in 49 participants (62%). Of 6 serious adverse events (7.6%) reported, 4 were deemed treatment-related (resolved).

In this intermediate analysis, reductions were seen in TAND-SQ, ABC scores, and severity of caregiver- and clinician-reported behavioral problems at 26 weeks after CBD initiation. The safety profile remained consistent with previous studies.

Authors/Disclosures
Elizabeth Thiele, MD (Massachusetts General Hospital)
PRESENTER
Dr. Thiele has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for GW Pharma/Jazz. Dr. Thiele has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for zogenix/UCB. Dr. Thiele has received personal compensation in the range of $500-$4,999 for serving as a Consultant for nobelpharma. Dr. Thiele has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Biocodex. Dr. Thiele has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Stoke Therapeutics. Dr. Thiele has received personal compensation in the range of $500-$4,999 for serving as a Consultant for livanova. Dr. Thiele has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Noema Pharma. Dr. Thiele has received personal compensation in the range of $500-$4,999 for serving as a Consultant for pyros pharmaceutical/upsher smith. Dr. Thiele has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Marinus Pharmaceuticals. The institution of Dr. Thiele has received research support from GW Pharma/Jazz. The institution of Dr. Thiele has received research support from Zogenix/UCB. The institution of Dr. Thiele has received research support from Stoke Therapeutics. The institution of Dr. Thiele has received research support from Biocodex. Dr. Thiele has received publishing royalties from a publication relating to health care.
Agnies van Eeghen, PhD The institution of Dr. van Eeghen has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Jazz Pharmaceuticals . The institution of Dr. van Eeghen has received research support from jazz pharmaceuticals . The institution of Dr. van Eeghen has received research support from ForWishdoem . The institution of Dr. van Eeghen has received research support from European Commission / ERN ITHACA .
Sarah L. Wilson, MD (UT Houston Medical School) Dr. Wilson has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Jazz Pharmaceuticals.
Stevie Roszkowski, PhD (University of Kentucky) Dr. Roszkowski has received personal compensation for serving as an employee of Jazz Pharmaceuticals. Dr. Roszkowski has stock in Jazz Pharmaceuticals.
maria dunaway-Bryant, Director of Clinical Operation Mrs. dunaway-Bryant has received personal compensation for serving as an employee of Jazz Pharmaceutical Company .
Kasia Wajer, BSC , MSc Miss Wajer has received personal compensation for serving as an employee of Jazz Pharmaceuticals . Miss Wajer has stock in Jazz Pharmaceuticals.
Teresa Greco Teresa Greco has nothing to disclose.
Joanne Stevens, BA (Jazz Pharmaceuticals) Ms. Stevens has stock in Jazz Pharmaceuticals.
Lisa Moore-Ramdin, MBBS Dr. Moore-Ramdin has received personal compensation for serving as an employee of Jazz Pharmaceuticals. Dr. Moore-Ramdin has stock in Jazz Pharmaceuticals.
Petrus J. de Vries, MBChB, FRCPsych, PhD The institution of Prof. de Vries has received research support from National Institute of Mental Health. The institution of Prof. de Vries has received research support from U.S. Department of Defense. Prof. de Vries has a non-compensated relationship as a Consultant with Jazz Pharmaceuticals that is relevant to AAN interests or activities.