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The primary objective of the study is to evaluate the efficacy of DSP-5423P compared with placebo in patients with schizophrenia.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
3 Sites
Beijing, Etc., China
53 Sites
Tokyo Etc., Japan
14 Sites
Kuala Lumpur, Etc., Malaysia
9 Sites
Manila, Etc., Philippines
8 Sites
Smolensk, Etc, Russia
7 Sites
Seoul, Etc., South Korea
6 Sites
Taipei, Etc., Taiwan
8 Sites
Poltava, Etc, Ukraine
Start Date
December 1, 2014
Primary Completion Date
December 1, 2018
Completion Date
December 1, 2018
Last Updated
April 12, 2022
580
ACTUAL participants
DSP-5423P Placebo
DRUG
DSP-5423P 40mg
DRUG
DSP-5423P 80mg
DRUG
DSP-5423P Placebo-to-Flex
DRUG
DSP-5423P Active-to-Flex
DRUG
Lead Sponsor
Sumitomo Pharma Co., Ltd.
NCT07455929
NCT06740383
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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