A Study to Evaluate Next Day Effects of TS-142 on Driving Performance in Healthy Subjects
NCT04696952 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 61
Last updated 2025-02-28
Summary
A clinical study to evaluate the residual effects of TS-142 on driving performance in healthy and elderly subjects.
Conditions
- Healthy Subjects
Interventions
- DRUG
-
TS-142
TS-142
- DRUG
-
Zopiclone
Zopiclone
- DRUG
-
Placebo
Sponsors & Collaborators
-
Taisho Pharmaceutical Co., Ltd.
lead INDUSTRY
Principal Investigators
-
Taisho Director · Taisho Pharmaceutical Co., Ltd.
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 21 Years
- Max Age
- 79 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-01-16
- Primary Completion
- 2022-01-05
- Completion
- 2022-01-05
Countries
- Japan
Study Locations
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