Thorough QT (TQT) Study to Evaluate the Effect of LC350189 on Cardiac Repolarization in Healthy Male and Female Subjects
Early Phase 1
Completed
- Conditions
- HyperuricemiaGoutQt Interval, Variation in
- Interventions
- Registration Number
- NCT04966325
- Lead Sponsor
- LG Chem
- Brief Summary
This is a Phase 1, single-center, randomized, partially double-blind, placebo- and positive controlled, 4-way crossover study to evaluate the effect of a therapeutic and a supratherapeutic dose of LC350189 on the QTcF in healthy male and female subjects.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 37
Inclusion Criteria
- The subject is 18 to 55 years of age, inclusive, with a body mass index (BMI) 18 to 33 kg/m2, inclusive, at screening.
- The subject is considered by the investigator to be in good general health as determined by medical history, clinical laboratory test results, vital sign measurements, 12-lead ECG results, and physical examination findings at screening.
- The subject is able to provide written informed consent and agrees to comply with all protocol requirements.
Exclusion Criteria
- The subject has a history of risk factors for torsades de pointes, including unexplained syncope, known long QT syndrome, heart failure, myocardial infarction, or angina.
- The subject has a family history of long QT syndrome, Brugada syndrome, or sudden death.
- The subject has a resting HR of <40 bpm or >100 bpm when vital signs are measured at screening or check-in.
- The subject has history or presence of unstable cardiovascular disease, including myocardial infarction, cardiac arrhythmia, or cerebrovascular disease (eg, cerebrovascular accident/stroke or transient ischemic attack).
- The subject has a history of other acute or chronic cardiovascular disease or coronary revascularization surgery (eg, coronary artery bypass graft, percutaneous transluminal coronary angioplasty).
- The subject uses a cardiac pacemaker.
- The subject has a history of any other medical, psychological, or social condition that, in the opinion of the investigator or the medical monitor, would prevent the subject from fully participating in the study, would represent a concern for study compliance, or would constitute a safety concern to the subject.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Treatment T (Therapeutic dose) LC350189 200mg Single oral dose of 200 mg LC350189 (1 × 200 mg tablet) and 2 × placebo tablets. Treatment P (Placebo) Placebo Single oral dose of 3 × placebo tablets. Treatment ST (Supratherapeutic dose) LC350189 600mg Single oral dose of 600 mg LC350189 (3 × 200 mg tablets). Treatment M (positive control) Moxifloxacin 400mg Single oral dose of moxifloxacin 400 mg (1 × 400 mg tablet; open label)
- Primary Outcome Measures
Name Time Method The placebo-corrected change from baseline in QTcF Before dosing (Baseline) through 24 hours after the dose on Day 1 in each treatment period QTcF will be analyzed using concentration-QT (cQT) modeling
- Secondary Outcome Measures
Name Time Method The placebo-corrected change from baseline in QRS Before dosing (Baseline) through 24 hours after the dose on Day 1 in each treatment period QRS will be evaluated at each postdose time point
The placebo-corrected change from baseline in HR (heart rate) Before dosing (Baseline) through 24 hours after the dose on Day 1 in each treatment period HR will be evaluated at each postdose time point
The placebo-corrected change from baseline in PR Before dosing (Baseline) through 24 hours after the dose on Day 1 in each treatment period PR will be evaluated at each postdose time point
Trial Locations
- Locations (1)
PPD
🇺🇸Austin, Texas, United States