The medical facility selected by Taisho Pharmaceutical Co., Ltd
Fukuoka, Japan
NCT Number: NCT04169906
The purpose of this study is to investigate the safety, pharmacokinetics, and pharmacodynamics of repeated dosing of TS-142 when administered once daily to healthy Japanese non-elderly participants.
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Notify Me20 year–39 year
Male
Interventional
Phase 1
Fukuoka, Japan
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive placebo once daily for 7 consective days
Participants will receive 10 mg of TS-142 once daily for 7 consective days
Participants will receive 20 mg of TS-142 once daily for 7 consective days
Participants will receive 30 mg of TS-142 once daily for 7 consective days
Time frame: Day 1 up to Day 14
Number of Treatment-emergent Adverse Events (TEAEs) and Serious AEs (SAEs) reported as mild, moderate, severe
Time frame: Day 1 up to Day 9
Concentration of TS-142 and its metabolites in plasma
Taisho Pharmaceutical Co., Ltd.
Industry
A Phase I Study of TS-142 in Non-Elderly Healthy Participants (Repeated Doses) (A Multiple Ascending Dose Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of TS-142 in Non-Elderly Participants)
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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