Tilman P.
- Country
- Germany
- Department
- Department for Epilepsy
Research Overview
- Evaluation of Radiprodil's Safety, Tolerability, and Pharmacokinetics in Pediatric GRIN-Related Disorder: A Multicenter Study
- Long-term Safety Evaluation of Fenfluramine Hydrochloride as Adjunctive Therapy in Patients with Myoclonic Astatic Epilepsy (Doose Syndrome)
- Open-label, Single-arm, Phase 3 Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Fenfluramine (Hydrochloride) in Infants 1 Year to less Than 2 Years of Age with Dravet Syndrome
Data & Insights
Has run more than one trial at 9 of 45 partner sites.
Specializations
Rare Epileptic Conditions
This investigator specializes in treating severe and rare epileptic disorders, with particular focus on Myoclonic Astatic Epilepsy (Doose Syndrome). Their research extends to managing complex seizure patterns in pediatric populations.
- Doose Syndrome Management
- Long-term Seizure Control
- Add-on Therapeutic Approaches
The investigator's work emphasizes innovative therapeutic strategies for treatment-resistant epilepsy cases.
Early-Onset Epilepsy
Focusing on Dravet syndrome in infants, the investigator studies therapeutic interventions for early-life epileptic conditions. Their expertise includes evaluating treatment responses in very young patients between ages 1-2 years.
- Infant Epilepsy Treatment
- Safety Monitoring in Young Patients
- Pharmacological Response Assessment
Special attention is given to developing safe and effective treatment protocols for infant populations.
Genetic Disorders
The investigator conducts research in CDKL5 Deficiency Disorder, exploring treatment options for this rare genetic condition. Their work encompasses both pediatric and adult patients affected by this disorder.
- Genetic Epilepsy Treatment
- Long-term Clinical Management
- Multi-age Treatment Strategies
Research focuses on developing comprehensive treatment approaches for genetic epileptic disorders.
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