A QT/QTc Evaluation Study of TS-142 in Healthy Adult Subjects

Healthy Subjects Clinical Trial

Official title:

A Study to Evaluate the Effects on QT/QTc Interval of TS-142 in Healthy Adult Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04873323
• Other study ID #: TS142-209
• Status: Completed
• Phase: Phase 1
• Start date: June 7, 2021
• Est. completion date: September 28, 2021

Study information

• Verified date: October 2021
• Source: Taisho Pharmaceutical Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A clinical study to evaluate the effects on QT/QTc Interval of TS-142 in Healthy Adult Subjects

Recruitment information / eligibility

• Status: Completed
• Enrollment: 59
• Est. completion date: September 28, 2021
• Est. primary completion date: September 28, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 39 Years

Eligibility

Inclusion Criteria:

• Japanese Males or females aged 20 years or older but less than 40 years at the time of informed consent
• those with a BMI of 18.5 in male (17.6 in female) or more and less than 25.0 and a body weight of 40.0 kg or more at screening test
• those whose pulse rate measured by standard 12-lead ECG is 50 beats/min or more but no more than 90 beats/min at screening test and at the time before administration of investigational drug in period 1
• those who are judged eligible to participate in the study by the principal investigator or sub-investigator based on the results of screening test and test conducted before administration of investigational drug in period 1. However, if who showed abnormal findings but not clinically significant, they can be enrolled in clinical trials based on comprehensive consideration of medical viewpoints by the principal investigator or subinvestigator.
• those who are able to receive the explanation before participating in the study, understand the content of the study, and provide written informed consent by the subjects themselves.

Exclusion Criteria:

• Subjects who have any disease and are not considered healthy subjects based on the medical judgment of the principal investigator or sub-investigator.
• Subjects with a medical history considered inappropriate for participation in the study, including respiratory, cardiovascular, gastrointestinal, hepatic, renal, urological, endocrine, metabolic, hematological, immune, skin, neurological, and psychiatric diseases.
• Subjects with a history of drug allergy or food allergy.
• Subjects with a history of hypersensitivity to moxifloxacin or other quinolone antimicrobials
• Subjects with risk factors or with a history of risk factors for aortic aneurysm, aortic dissection (such as Marfan syndrome)
• Subjects with significant allergic predisposition (such as asthma requiring medical treatment)
• Subjects with congenital disease, heart disease, or a history of heart disease
• Subjects with risk factors or with a history of risk factors for torsade de pointes (TdP) (heart failure, hypokalemia, family history of long QT syndrome, etc.)
• Subjects with a history of unconscious seizures suspected of involving TdP.
• Subjects with waveforms difficult to assess for QTc interval prolongation in standard 12-lead ECG at screening and the timing before administration of investigational product in period 1 (drift, electromyography contamination, T-wave geometry, marked sinus arrhythmia, frequent premature beats, etc.)
• Subjects with QTcF(Fridericia correction method) of at least 450 msec in men and at least 470 msec in women in standard-12-lead ECG at screening test and at the time before administration of investigational product in period 1.
• Subjects with suicidal ideation, suicide attempt on the Colombian Suicide Assessment Scale (C-SSRS) on Day-1 or a history of suicide attempt within the previous 5 years.
• Other protocol defined inclusion criteria could apply

Related Conditions & MeSH terms

• Healthy Subjects

Intervention

Drug:
• TS-142
Single dose of TS-142 10 mg or TS-142 30 mg in the morning under fasting in each period
• Moxifloxacin
Single dose of moxifloxacin 400 mg in the morning under fasting in each period
• Placebo
Single dose of TS-142 placebo in the morning under fasting in each period

Locations

Country	Name	City	State
Japan	Taisho Pharmaceutical Co., Ltd selected site	Toshima-ku

Sponsors (1)

Lead Sponsor	Collaborator
Taisho Pharmaceutical Co., Ltd.

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	QTcF:QT-interval corrected by Fridericia corrections in Holter ECGs	Difference (??QTc) in change from baseline (?QTc) in QTc interval at each time point in each group compared with the placebo group	Up to 24 hours postdose during each period