Finding studies
Finding studies
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Lead
Sumitomo Pharma America, Inc.
This study will be conducted at a single site as a double-blind, placebo-controlled, mulitple ascending oral doses evaluation of the safety, tolerability, and pharmacokinetics of DSP-1053 and its metabolites in healthy subjects with Major depressive disorder after the minimumally intolerated dose is reached in healthy subjects
Age
18–50
Sex
ALL
Healthy volunteers
Accepted
