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A phase I study of STN1013600 ophthalmic solution in healthy adult male volunteer

Phase 1
Conditions
Presbyopia
Registration Number
JPRN-jRCT2031210614
Lead Sponsor
Migita Yukie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
24
Inclusion Criteria

Subjects who can comply with scheduled visits, the examination and observation as specified in
the clinical study protocol

Exclusion Criteria

1)Subjects have a disease and/or abnormal laboratory value which is considered inappropriate from safety evaluation perspective
2)Subjects who are inappropriate as participants in this study in the opinion of the investigator or sub investigator

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Safety: Adverse events and adverse drug reactions
Secondary Outcome Measures
NameTimeMethod
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