Distinguished in Autosomal Dominant Partial Epilepsy with Auditory Features

Dr. Pavel Klein

Neurology

6410 Rockledge Dr, Suite 610,

Bethesda, MD

Accepting New Patients

Offers Telehealth

Distinguished in Autosomal Dominant Partial Epilepsy with Auditory Features

6410 Rockledge Dr, Suite 610,

Bethesda, MD

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Overview

Pavel Klein is a Neurologist in Bethesda, Maryland. Dr. Klein is rated as a Distinguished provider by MediFind in the treatment of Autosomal Dominant Partial Epilepsy with Auditory Features. His top areas of expertise are Seizures, Epilepsy, Generalized Tonic-Clonic Seizure, and Post-Traumatic Epilepsy. Dr. Klein is currently accepting new patients.

His clinical research consists of co-authoring 97 peer reviewed articles and participating in 11 clinical trials. MediFind looks at clinical research from the past 15 years.

Specialties

Neurology

Licenses

Psychiatry & Neurology in MD

Languages Spoken

English

Czech

German

Russian

Gender

Male

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Locations

6410 Rockledge Dr, Suite 610, Bethesda, MD 20817

Call: 301-530-9744

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers 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.

11 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)

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 Adult Subjects With Lennox-Gastaut Syndrome (LGS)