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Phase1 Study of TS-141 in Healthy Volunteers

Phase 1
Completed
Conditions
-
Registration Number
JPRN-jRCT2080225139
Lead Sponsor
Taisho Pharmaceutical Co.Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
completed
Sex
Male
Target Recruitment
48
Inclusion Criteria

Healthy Volunteers

Exclusion Criteria

Patients with a current medical history or medical history deemed inappropriate for participation in this study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
safety<br>pharmacokinetics<br>To investigate Pharmacokinetics parameter of TS-141 and its metabolite<br>To investigate incidence of Treatment-emergent Adverse Events and Serious AEs, vital-sign, weight, 12-leads ECG and clinical laboratory test
Secondary Outcome Measures
NameTimeMethod
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