drugset / Trial / NCT04325737

Study Assessing the Safety, Tolerability, and Pharmacokinetics of SEP-363856 in Japanese Male and Female Subjects With Schizophrenia

NCT04325737

Phase 1 Completed 13 enrolled Sumitomo Pharma Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multiple oral dose, randomized, double-blind, placebo-controlled study assessing the safety, tolerability and pharmacokinetics (PK) of SEP-363856 when administered qhs to Japanese subjects with schizophrenia.

Timeline

Start
2020-03-31
Primary completion
2020-08-07
Completion
2020-08-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Ulotaront Small molecule 100 mg Oral

Indications