A Phase 3, Placebo-Controlled Study to Investigate LP352 in Children and Adults With Dravet Syndrome (DS)
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Investigate the Efficacy, Safety, and Tolerability of LP352 in the Treatment of Seizures in Children and Adults With Dravet Syndrome
2 other identifiers
interventional
160
17 countries
97
Brief Summary
This (DEEp SEA Study) is a double-blind, randomized, placebo-controlled, multicenter study to investigate the efficacy, safety, and tolerability of LP352 in the treatment of seizures in children and adults with DS. The study consists of 3 main phases: Screening, Titration period, and Maintenance period, followed by a Taper period and Follow-Up. Participants will be randomized to LP352 or placebo. The total duration of the study will be approximately 24 months.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_3
Started Sep 2024
97 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 25, 2024
CompletedFirst Submitted
Initial submission to the registry
October 24, 2024
CompletedFirst Posted
Study publicly available on registry
October 28, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 21, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
October 2, 2026
April 15, 2026
April 1, 2026
1.9 years
October 24, 2024
April 13, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Frequency Percent Change in Countable Motor Seizures During Treatment Compared to Baseline
The percent change from Baseline in countable motor seizure frequency during Treatment will be calculated as countable motor seizure frequency during Treatment minus countable motor seizure frequency during Screening and divided by seizure frequency during Screening and multiplied by 100 where each seizure frequency will be based on number of seizures.
Baseline and up to 15 Weeks
Secondary Outcomes (3)
Safety and Tolerability of LP352
Up to 21 Weeks
Percentage of participants with ≥ 50% Reduction in countable motor seizures during Treatment compared to Baseline
Baseline and up to 15 Weeks
Frequency Percent Change in Countable Motor Seizures during Maintenance compared to Baseline
Baseline and up to 15 Weeks
Study Arms (2)
LP352
EXPERIMENTALParticipants will be titrated up to highest tolerated dose of LP352 during the Titration period (Visit 2 - Visit 5), followed by maintenance period (Visit 5 - Visit 8) and then taper/down titration period.
Placebo
PLACEBO COMPARATORPlacebo for LP352
Interventions
Eligibility Criteria
You may qualify if:
- Diagnosis of DS must fulfill all of the following criteria:
- Participants with seizure onset age \>1 and \<20 months
- The participant has a history of at least 1 of the following seizure type(s): prolonged generalized tonic-clonic, hemiclonic, myoclonic, tonic, atonic, atypical absence, focal impaired awareness, nonconvulsive status epilepticus
- The participant has a current occurrence of at least 1 of the following countable motor seizure types: generalized tonic-clonic, tonic (bilateral), clonic (bilateral), atonic (bilateral) with truncal/leg involvement, focal motor (including hemiclonic), and focal to bilateral tonic-clonic
- The participant has demonstrated an average of at least 4 countable motor seizures per month for the 3 months prior to Screening.
- The participant has been taking 1 to 4 antiseizure medications (ASMs) at a stable dose for at least 4 weeks prior to Screening.
- The participant, parent, or caregiver is willing and able (in the judgment of the investigator) to comply with completion of the diaries throughout the study.
- The participant must be willing and able to provide written informed consent.
You may not qualify if:
- The participant has a history of infantile/epileptic spasms.
- The participant has been admitted to a medical facility for treatment of status epilepticus requiring mechanical ventilation within 3 months prior to Screening.
- The participant has a neurodegenerative disorder as indicated by magnetic resonance imaging or genetic testing.
- The participant has an acquired lesion/injury unrelated to the primary etiology that could contribute as a secondary cause of seizures.
- The participant is currently using any cannabis product or cannabidiol that is not in oral solution/capsule/tablet form, not obtained from a government-approved dispensary, or contains ≥50% Delta-9-tetrahydrocannabinol (THC).
- The participant has unstable, clinically significant neurologic (other than the disease being studied, eg, recurrent strokes), psychiatric, cardiovascular (eg, pulmonary arterial hypertension, cardiac valvulopathy, orthostatic hypotension/tachycardia), pulmonary, hepatic, renal, metabolic, gastrointestinal, urologic, immunologic, hematopoietic, or endocrine disease or other abnormality which may impact the ability of the participant to participate or potentially confound the study results.
- The participant is unwilling to comply with any of the study requirements or timelines.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (97)
Arkansas Children's Hospital - PIN
Little Rock, Arkansas, 72202-3500, United States
Children's Hospital Los Angeles - PIN
Los Angeles, California, 90027-6062, United States
David Geffen School of Medicine at UCLA
Los Angeles, California, 90095-3075, United States
The Stanford Division of Child Neurology
Palo Alto, California, 94304-1510, United States
UCSF Children's Hospital
San Francisco, California, 94143-2350, United States
Children's Hospital Colorado.
Aurora, Colorado, 80045-7106, United States
NW FL Clinical Research Group, LLC
Gulf Breeze, Florida, 32561-4458, United States
Nicklaus Children's Hospital - PIN
Miami, Florida, 33155-3009, United States
Research Institute of Orlando LLC
Orlando, Florida, 32806-5411, United States
Pediatric Epilepsy and Neurology Specialists
Tampa, Florida, 33609-4190, United States
Rare Disease Research, LLC - Atlanta - RDR - PIN
Atlanta, Georgia, 30329, United States
Ann and Robert H Lurie Childrens Hospital of Chicago - PIN
Chicago, Illinois, 60611, United States
Mid-Atlantic Epilepsy and Sleep Center
Bethesda, Maryland, 20817-1844, United States
Mayo Clinic - PIN
Rochester, Minnesota, 55905-0001, United States
Institute of Neurology and Neurosurgery at Saint Barnabas, LLC
Livingston, New Jersey, 07039-5817, United States
Northeast Regional Epilepsy Group - Morristown - 310 Madison Ave
Morristown, New Jersey, 07960, United States
NYU Comprehensive Epilepsy Center - BRANY - PPDS
New York, New York, 10016-4852, United States
Oregon Health and Science University
Portland, Oregon, 97239-3011, United States
Le Bonheur Childrens Outpatient Center - PIN
Memphis, Tennessee, 38103-2816, United States
Child Neurology Consultants of Austin - 6811 Austin Center Blvd
Austin, Texas, 78757, United States
Cook Children's Jane and John Justin Neurosciences Center - PIN
Fort Worth, Texas, 76104-2710, United States
The University of Texas Medical School at Houston
Houston, Texas, 77030, United States
Multicare Health System - Mary Bridge Pediatrics
Tacoma, Washington, 98405, United States
Prince of Wales Hospital
Randwick, New South Wales, 2031, Australia
Sydney Children's Hospital
Randwick, New South Wales, 2031, Australia
Children's Hospital at Westmead
Westmead, New South Wales, 2145, Australia
Royal Brisbane & Women's Hospital
Herston, Queensland, 4029, Australia
Queensland Children's Hospital
South Brisbane, Queensland, 4101, Australia
Austin Hospital
Heidelberg, Victoria, 3084, Australia
Royal Children's Hospital Melbourne
Parkville, Victoria, 3052, Australia
The Alfred Hospital
Melbourne, 3004, Australia
UZ Leuven
Leuven, Vlaams Brabant, 3000, Belgium
UZ Antwerpen
Antwerp, 2650, Belgium
Instituto de Neurologia de Curitiba (INC)
Curitiba, Paraná, 81210-310, Brazil
Hospital Das Clinicas da Faculdade de Medicina de Ribeirão Preto - USP - PPDS
Ribeirão Preto, São Paulo, 14051-140, Brazil
Fundacao Faculdade Regional de Medicina de Sao Jose Do Rio Preto Hospital de Base - PPDS
São José do Rio Preto, São Paulo, 15090-000, Brazil
Instituto de Psiquiatria HC FMUSP
São Paulo, 05403-010, Brazil
Children's and Women's Health Centre of British Columbia-4480 Oak St
Vancouver, British Columbia, V6H 3V4, Canada
London Health Sciences Centre -800 Commissioners Rd E
London, Ontario, N6A 5W9, Canada
Hospital For Sick Children
Toronto, Ontario, M5G 1X8, Canada
Toronto Western Hospital
Toronto, Ontario, M5T 2S8, Canada
Peking University First Hospital - Daxing Campus
Beijing, Beijing Municipality, 102627, China
The Second Affiliated Hospital of Guangzhou Medical University
Guangzhou, Guangdong, 510260, China
Shenzhen Children's Hospital
Shenzhen, Guangdong, 518000, China
Wuhan Children's Hospital
Wuhan, Hubei, 430010, China
Children's Hospital of Fudan University
Shanghai, Shanghai Municipality, 201102, China
Beijing Children's Hospital, Capital Medical University - PIN
Beijing, 100045, China
Hôpital Roger Salengro
Lille, Nord, 59000, France
Hospices Civils de Lyon - Hôpital Pierre Wertheimer
Bron, 69500, France
AP-HM- Hôpital de La Timone
Marseille, 13386, France
Hôpital Necker - Enfants Malades
Paris, 75015, France
AP-HP - Hôpital universitaire Robert-Debré
Paris, 75019, France
CHU de Rennes - Hôpital Pontchaillou
Rennes, 35203, France
CHU de Strasbourg - Hôpital de Hautepierre
Strasbourg, 67098, France
Centre Hospitalier Universitaire de Toulouse
Toulouse, 31330, France
Klinikum der Johann-Wolfgang Goethe-Universitat
Frankfurt am Main, Hesse, 60596, Germany
Universitätsklinikum Bonn
Bonn, North Rhine-Westphalia, 53127, Germany
Gesellschaft für Epilepsieforschung e.V.
Bielefeld, 33617, Germany
Universitätsklinikum Schleswig-Holstein - Campus Kiel
Kiel, 24105, Germany
Epilepsie-Zentrum Bodensee
Ravensburg, 88214, Germany
IRCCS Ospedale Pediatrico Bambino Gesù - INCIPIT - PIN
Roma, 00165, Holy See
Fondazione Policlinico Universitario A Gemelli - Rome - PPDS
Rome, Lazio, 00168, Italy
Fondazione Istituto Neurologico Nazionale Casimiro Mondino IRCCS
Pavia, Lombardy, 27100, Italy
Azienda Ospedaliero Universitaria A Meyer - INCIPIT - PIN
Florence, Tuscany, 50139, Italy
Azienda Ospedaliera Universitaria Integrata Di Verona
Verona, Veneto, 37126, Italy
Istituto G Gaslini Ospedale Pediatrico IRCCS - INCIPIT - PIN
Genova, 16147, Italy
IUHW Narita Hospital
Narita-shi, Chiba, 286-8520, Japan
Hokkaido University Hospital
Sapporo, Hokkaidô, 060-8648, Japan
Fukuoka Children's Hospital
Fukuoka, Hukuoka, 813-0017, Japan
National Hospital Organization Nishi-Niigata Chuo National Hospital
Niigata, Niigata, 950-2074, Japan
Okayama University Hospital
Okayama, Okayama-ken, 700-8558, Japan
Saitama Prefectural Children's Medical Center
Saitama-shi, Saitama, 330-8777, Japan
National Hospital Organization Shizuoka Institute of Epilepsy and Neurological Disorders
Shizuoka, Shizuoka, 420-0953, Japan
Dokkyo Medical University Hospital
Mibu-Machi, Tochigi, 321-0293, Japan
National Center of Neurology and Psychiatry
Kodaira-Shi, Tokyo, 187-8502, Japan
Osaka City General Hospital
Osaka-Shi Miyakojima-Ku, Ôsaka, 534-0021, Japan
Children's Clinical University Hospital
Riga, LV-1004, Latvia
Instituto Nacional de Pediatría
Mexico City, 4530, Mexico
ULS de Coimbra, EPE - Hospital Pediátrico de Coimbra
Coimbra, 3000-602, Portugal
ULS de Santa Maria,EPE - Hospital de Santa Maria - PPDS
Lisbon, 1649-035, Portugal
ULS de Santo António, EPE - Centro Materno Infantil Norte
Porto, 4050-651, Portugal
University Clinical Center of Serbia - Dr Subotica 6 - PPDS
Belgrade, Belgrade, 11000, Serbia
Clinic for Neurology and Psychiatry for Children and Youth
Belgrade, 11000, Serbia
Mother and Child Health Care Institute of Serbia Dr Vukan Cupic
Belgrade, 11000, Serbia
University Clinical Center Kragujevac
Kragujevac, 34000, Serbia
Hospital Sant Joan de Deu - PIN
Espluges de Llobregat, Barcelona, 08950, Spain
Hospital Regional Universitario de Malaga - Hospital General
Málaga, Málaga, 29010, Spain
Hospital Universitario de Navarra
Pamplona, Navarre, 31008, Spain
Hospital Universitario Vall d'Hebron - PPDS
Barcelona, 08035, Spain
Hospital de La Santa Creu i Sant Pau
Barcelona, 8041, Spain
Hospital Universitario Vithas Madrid La Milagrosa
Madrid, 28010, Spain
Hospital Ruber Internacional (Grupo Quironsalud)
Madrid, 28034, Spain
Hospital Vithas Malaga
Málaga, 29016, Spain
Royal Victoria Infirmary
Newcastle upon Tyne, Northamptonshire, NE1 4LP, United Kingdom
Queen Elizabeth University Hospital - PPDS
Glasgow, G51 4TF, United Kingdom
University College London Hospitals (UCLH) - PPDS
London, NW1 2PG, United Kingdom
Great Ormond Street Hospital - PPDS
London, WC1N 3JH, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 24, 2024
First Posted
October 28, 2024
Study Start
September 25, 2024
Primary Completion (Estimated)
August 21, 2026
Study Completion (Estimated)
October 2, 2026
Last Updated
April 15, 2026
Record last verified: 2026-04