- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT07634484
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
Přehled studie
Postavení
Podmínky
Intervence / Léčba
Typ studie
Zápis (Odhadovaný)
Fáze
- Fáze 4
Kontakty a umístění
Studijní kontakt
- Jméno: Kaho Ikegami
- Telefonní číslo: 81-3-3279-7454
- E-mail: ctrdinfo@kowa.co.jp
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Popis
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).
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Randomizované
- Intervenční model: Paralelní přiřazení
- Maskování: Čtyřnásobek
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Komparátor placeba: Placebo
|
Podává se perorálně jednou denně
|
|
Experimentální: Pemafibrate 0.2mg/day
|
Administered orally once daily
|
|
Experimentální: Pemafibrate 0.4mg/day
|
Administered orally once daily
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Percentage change from baseline in LDL-C (direct)
Časové okno: 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
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Achievement of lipid management targets based on the mean LDL-C (direct) values
Časové okno: 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
Časové okno: 4, 8, and 12 weeks after administration
|
4, 8, and 12 weeks after administration
|
Spolupracovníci a vyšetřovatelé
Sponzor
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Odhadovaný)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Další relevantní podmínky MeSH
Další identifikační čísla studie
- PALT03
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .