The clinical study is expected to enroll about 348 subjects from up to 40 different centers in the U.S, Canada, and Europe for a 12-week double-blind treatment phase, followed by a 52-week open-label extension phase.
With the BTD, the US FDA will provide additional support and guidance to a quicker path to a NDA application.
“Existing pharmacotherapies for schizophrenia is limited in their efficacy. Our SND13 study presents a new, patient-centered treatment approach for schizophrenia patients, to bring up the much needed social skills and cognitions in order to improve patients’ overall daily functioning at work and/or home” said the CEO and Chairman of SyneuRx International (Taiwan) Corp, Emil Tsai, MD, PhD, MAS.
About SND13 study
To learn more about the SND13 study, please click http://syneurxtrials.com/Trials/Adult-Schizophrenia for more information about study and recruitment.
About SyneuRx International (Taiwan) Corp.
SyneuRx (6575) is a global biotech company listed at the Emerging Board of Taiwan. The company specializes in the development of new-class drug therapies for CNS disorders. Several programs are currently in progress in late-phase clinical trials or late-phase clinical trials ready in major CNS conditions including schizophrenia, dementia, and depression.