Status:
COMPLETED
Bioequivalence Study of Oral Suspension and Intravenous Formulation of Edaravone in Healthy Adult Subjects
Lead Sponsor:
Tanabe Pharma Corporation
Conditions:
Healthy Adult Subjects
Eligibility:
All Genders
20-45 years
Phase:
PHASE1
Brief Summary
To evaluate the single-dose bioequivalence of oral suspension and intravenous (IV) formulation of edaravone in the fasting state in healthy adult subjects
Eligibility Criteria
Inclusion
- Healthy adult male or female volunteers
- Japanese
- Subjects aged between 20 and 45 years at the time of informed consent
- Subjects who have thoroughly understood the contents of the study and voluntarily provided written informed consent to participate in the study
Exclusion
- Additional screening criteria check may apply for qualification:
- Subjects with a current or previous history of cardiac, hepatic, renal, gastrointestinal, respiratory, psychiatric/nervous, hematopoietic, or endocrine diseases, and those whom the investigator (or subinvestigator) deems unsuitable for the study
- Body mass index (BMI) of \<18.0 or \>30.0, or body weight of \<50 kg (BMI formula: body weight \[kg\]/height \[m\]2, rounded to one decimal place)
- Subjects who have undergone any surgery known to affect the gastrointestinal absorption of drugs
- Female subjects who do not agree to use an effective method of contraception from screening or 2 weeks before the start of investigational product administration, whichever comes earlier, to 14 days after the completion (or discontinuation) of investigational product administration. Male subjects who do not agree to use an effective method of contraception from the start of investigational product administration to 14 days after the completion (or discontinuation) of investigational product administration
- Subjects who have previously received edaravone
- Subjects who have participated in another clinical study and received an investigational product within 12 weeks before providing informed consent
Key Trial Info
Start Date :
March 22 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 9 2019
Estimated Enrollment :
42 Patients enrolled
Trial Details
Trial ID
NCT04493281
Start Date
March 22 2019
End Date
May 9 2019
Last Update
January 7 2026
Active Locations (1)
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1
Investigational site
Tokyo, Japan