OP-724-001 study
- Conditions
- Healthy volunteers
- Registration Number
- JPRN-jRCT2031230432
- Lead Sponsor
- Yuushi Haruyama
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Male
- Target Recruitment
- 6
1: Healthy Japanese male subjects.
2: Age at the time of obtaining written informed consent is >=18 to <45 years old.
3: Subjects who are capable of fully understanding the clinical trial and providing written informed consent.
1: Subjects with any clinilcal abnormality assessed by the investigator or subinvestigator in laboratory tests, vital signs, or 12-lead ECG in eligibility testing.
2: Subjects with a QTcF of > 450 msec on a 12-lead ECG in the eligibility test.
3: Subjects who weighs < 50.0 kg in the eligibility test.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pharmacokinetics
- Secondary Outcome Measures
Name Time Method Satety