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Clinical Trial Summary

A Phase 2 Study to Assess the Safety, Tolerability, Exploratory Efficacy, and pharmacokinetics of Orally Administered JBPOS0101 for Refractory Infantile Spasms Patients.


Clinical Trial Description

This open label, multicenter study allowed JBPOS0101 (investigational product) to be given as either add-on therapy or monotherapy for patients with refractory infantile spasms. The design and choice of study population of this Phase 2 clinical study was based on the need to provide initial safety, tolerability, pharmacokinetics (PK), and efficacy outcomes of the investigational product for future clinical studies. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03976076
Study type Interventional
Source Bio-Pharm Solutions Co., Ltd.
Contact
Status Terminated
Phase Phase 2
Start date April 15, 2020
Completion date December 10, 2021