A Post-Marketing Clinical Trial of Pemafibrate in Patients with Hypercholesterolemia and Inadequate Response to Statins
A Post-Marketing Clinical Trial of Pemafibrate in Patients With Hypercholesterolemia and Inadequate Response to Statins-Multicenter, Placebo Controlled, Randomized, Double Blind, Parallel Group Controlled Trial
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Phase
Phase
- Phase 4
Contacts and Locations
Study Contact
Study Contact
- Name: Kaho Ikegami
- Phone Number: 81-3-3279-7454
- Email: ctrdinfo@kowa.co.jp
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:Patients who meet all the following criteria shall be eligible for the clinical trial.
- Patients with hypercholesterolemia aged 18 years or older at the time of obtaining written informed consent
- Patients who have taken statins at a fixed dose and regimen within the approved dose range for at least four weeks prior to the first screening assessment.
- Patients who have received stable dietary and/or exercise therapy for at least 12 weeks prior to the first screening assessment.
- Patients with the fasting serum TG < 150 mg/dL on two consecutive occasions at screening
Patients who apply any of the following risk category with LDL-C level (direct) based on JAS2022 on two consecutive occasions at screening
- Low risk for primary prevention: LDL-C >=160 mg/dL
- Intermediate risk for primary prevention: LDL-C >=140 mg/dL
- High risk for primary prevention: LDL-C>=120 mg/dL or 100 mg/dL*
- Secondary prevention: LDL-C>=100 mg/dL
Familial hypercholesterolemia (heterozygous): LDL-C>=100 mg/dL
- For patients with diabetes, those with peripheral artery disease (PAD), microvascular complications (retinopathy, nephropathy, neuropathy), or current smoking are included if LDL-C>=100 mg/dL.
Exclusion Criteria:Patients who meet any of the following criteria will be excluded from the clinical trial.
- Patients who require administration of prohibited drugs during the post-marketing clinical trial period after written informed consent
- Patients with type 1 diabetes and uncontrolled type 2 diabetes [HbA1c(NGSP) >= 10.0 % at Screening]
- Patients whose LDL-C level changed by more than +20% or -20% in the second screening test compared to the the first.
- Patients with uncontrolled thyroid disease
- Patients who are undergoing or are scheduled to undergo LDL apheresis
- Patients with cirrhosis or those with biliary obstruction
- Patients with gallstones
- Patients with familial hypercholesterolemia (homozygotes)
- Patients with impaired renal function (eGFR < 30 mL/min/1.73 m2 at screening)
- Patients with uncontrolled hypertension (SBP >= 160 mmHg or DBP >= 100 mmHg) at screening
- Patients with AST and ALT levels three times or greater than the upper limit of normal at screening
- Patients with CK levels at least three times the upper limit of normal at screening
- Patients with any of the following experiences within 3 months prior to informed consent: myocardial infarction, severe or unstable angina pectoris, coronary angioplasty, coronary artery bypass surgery, stroke, transient ischemic attack, symptomatic carotid artery stenosis, symptomatic peripheral arterial disease, abdominal aortic aneurysm, uncontrolled severe arrhythmia and decompensated heart failure
- Patients who plan to undergo PCI, CABG, carotid artery or peripheral revascularization
- Patients with heart failure class III or higher according to NYHA cardiac function classification
- Patients with malignant tumor or those who are judged to have a high risk of recurrence
- Patients with a history of myopathy or rhabdomyolysis due to pemafibrate
- Patients with a history of hypersensitivity due to pemafibrate
- Patients with a history of serious drug allergies (anaphylactic shock, etc.)
- Pregnant women, lactating women, women planning to become pregnant or lactating during the study period, or pregnant women of childbearing potential*2 who do not use specific contraceptive methods*1
- Patients who have undergone whole blood donation of 400 mL or more within 16 weeks, or 200 mL or more within 4 weeks, or component donation (plasma or platelet donation) within 2 weeks prior to screening.
- Patients with alcoholics or drug addicts
- Patients who participated in other clinical trials of a drug with new active ingredients within 16 weeks or a drug with an approved active ingredients within 12 weeks prior to administration and received an investigational drug other than placebo,or those who will participate in other clinical trials at the same time as the clinical trial
Patients who are considered inappropriate for participation in this study by the investigator, etc
- 1 Acceptable contraceptive methods: Oral hormonal contraceptives (combination pills containing progestin and estrogen), intrauterine devices, intrauterine hormonal delivery systems, abstinence
2 Woman of childbearing potential refers to a woman who is physiologically capable of becoming pregnant with a male partner who has not undergone contraception. However, it does not apply if the investigator confirms that any of the following criteria is met.
- Patients with hysterectomy or tubal ligation before informed consent
- Post-menopausal women (those who have passed more than 1 year since their last menstrual period without other medical reasons).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Placebo Comparator: Placebo
|
Administered orally once daily
|
|
Experimental: Pemafibrate 0.2mg/day
|
Administered orally once daily
|
|
Experimental: Pemafibrate 0.4mg/day
|
Administered orally once daily
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage change from baseline in LDL-C (direct)
Time Frame: 4, 8, and 12 weeks after administration
|
Percent change = (measured value at each time point - baseline value) / baseline value
|
4, 8, and 12 weeks after administration
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Achievement of lipid management targets based on the mean LDL-C (direct) values
Time Frame: 4, 8, and 12 weeks after administration
|
Calculate the percentage of participants who achieved lipid management targets
|
4, 8, and 12 weeks after administration
|
|
Percentage change from baseline in LDL-C(Friedewald formula), HDL-C(direct), non-HDL-C, TC, TG
Time Frame: 4, 8, and 12 weeks after administration
|
4, 8, and 12 weeks after administration
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- PALT03
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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