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Clinical Trials/JPRN-UMIN000033055
JPRN-UMIN000033055Completed未知

Clinical study about in vitro - in vivo correlation in supersaturation of poorly soluble basic drug - Clinical study about IVIVC in poorly soluble basic drug

Ritsumeikan University0 sites18 target enrollmentStarted: June 19, 2018Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Enrollment
18

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20years-old to 40years-old (—)
Sex
Male

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1. Subjects who had gastrointestinal resection and vagotomy 2. Subjects with present illness which requires treatment. 3. Subjects with past medical history which was considered not adequate for this study. 4. Subjects with past history of drug allergy. 5. Subjects who took prescribed medicine and/or OTC drug 1 week prior to admission of period 1. 6. Subjects who donated and/or withdrawn whole blood more than 400mL within 12 weeks, 200 mL within 4 weeks, and/or blood component within 2 weeks prior to admission of period 1. 7. Subjects who participated in a clinical trial and was administered study drug within 16 weeks prior to admission of period 1. 8. Subjects with history of alcohol and/or drug abuse. 9. Subjects who were judged not appropriate for this study by study physician.

Investigators

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