Distinguished in Partial Familial Epilepsy

Wei-ping B. Liao

Key Laboratory Of Neurogenetics And Channelopathies Of Guangdong Province And The Ministry Of Education Of China, 
Guangzhou, CN 
Distinguished in Partial Familial Epilepsy
Key Laboratory Of Neurogenetics And Channelopathies Of Guangdong Province And The Ministry Of Education Of China, 
Guangzhou, CN 
OverviewLocationsClinical Research

Overview

Wei-ping Liao practices in Guangzhou, China. Liao is rated as a Distinguished expert by MediFind in the treatment of Partial Familial Epilepsy. Their top areas of expertise are Genetic Epilepsy with Febrile Seizures Plus (GEFS+), Partial Familial Epilepsy, Epilepsy, Lennox-Gastaut Syndrome (LGS), and Lithotripsy.

Their clinical research consists of co-authoring 80 peer reviewed articles and participating in 3 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 4 articles in the study of Partial Familial Epilepsy.

Locations

Key Laboratory Of Neurogenetics And Channelopathies Of Guangdong Province And The Ministry Of Education Of China, Guangzhou, China
Other Locations
Wuhan, 430030, China
Guangdong Provincial Key Laboratory Of Micro/Nano Optomechatronics Engineering, Shenzhen, 518060, China

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

3 Clinical Trials

A Phase 3, Prospective, Open-Label, Multisite, Extension of Phase 3 Studies To Assess the Long-Term Safety and Tolerability of Soticlestat as Adjunctive Therapy in Subjects With Dravet Syndrome or Lennox-Gastaut Syndrome (ENDYMION 2)
A Phase 3, Prospective, Open-Label, Multisite, Extension of Phase 3 Studies To Assess the Long-Term Safety and Tolerability of Soticlestat as Adjunctive Therapy in Subjects With Dravet Syndrome or Lennox-Gastaut Syndrome (ENDYMION 2)
Enrollment Status: Terminated
Publish Date: October 08, 2025
Intervention Type: Drug
Study Drug: Soticlestat
Study Phase: Phase 3
A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy, Safety, and Tolerability of Soticlestat as Adjunctive Therapy in Pediatric and Young Adult Subjects With Dravet Syndrome (DS)
A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy, Safety, and Tolerability of Soticlestat as Adjunctive Therapy in Pediatric and Young Adult Subjects With Dravet Syndrome (DS)
Enrollment Status: Completed
Publish Date: January 01, 2025
Intervention Type: Drug
Study Drug: Soticlestat
Study Phase: Phase 3
A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy, Safety, and Tolerability of Soticlestat as Adjunctive Therapy in Pediatric and Adult Subjects With Lennox-Gastaut Syndrome (LGS)
A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy, Safety, and Tolerability of Soticlestat as Adjunctive Therapy in Pediatric and Adult Subjects With Lennox-Gastaut Syndrome (LGS)
Enrollment Status: Completed
Publish Date: August 21, 2024
Intervention Type: Drug
Study Drug: Soticlestat
Study Phase: Phase 3
View 2 Less Clinical Trials

80 Total Publications

Variants in CSMD2 and CSMD3, genes involved in synaptogenesis, are associated with epilepsies.
Variants in CSMD2 and CSMD3, genes involved in synaptogenesis, are associated with epilepsies.
Journal: Epilepsia
Published: March 17, 2025

Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

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