- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT07684469
Comparative Assessment of Inclisiran on Top of Standard of Care Versus Standard of Care Alone for LDL-C Evaluation in Acute Coronary Syndrome Patients in Saudi Arabia
Comparative, Randomized, Multicenter, Followed by an Open Label Extension Trial in Patients With a Recent Acute Coronary Syndrome Evaluating the Early Inclusion of Inclisiran Into Standard of Care Versus Standard of Care Alone in Kingdom of Saudi Arabia
Přehled studie
Postavení
Podmínky
Intervence / Léčba
Detailní popis
Typ studie
Zápis (Odhadovaný)
Fáze
- Fáze 4
Kontakty a umístění
Studijní kontakt
- Jméno: Novartis Pharmaceuticals
- Telefonní číslo: +41613241111
- E-mail: novartis.email@novartis.com
Studijní záloha kontaktů
- Jméno: Novartis Pharmaceuticals
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Popis
Inclusion Criteria:
Participants eligible for inclusion in this study must meet all of the following criteria:
- Males and females ≥18 years of age.
- Recent ACS (in-patient/out-patient) within 7 days of index admission, as per 2023 ESC guidelines for the management of acute coronary syndrome
- Serum LDL-C ≥1.8 mmol/L (≥70 mg/dL) or non-HDL ≥100 mg/dL at screening for participants who were receiving SOC [including lipid lowering therapy and/or ezetimibe] prior enrollment.
- Serum LDL-C ≥2.6 mmol/L (≥100 mg/dL) or non-HDL ≥124 mg/dL at screening for participants who were SOC treatment naïve prior enrollment.
- Fasting triglycerides <4.52 mmol/L (<400 mg/dL) at screening.
- Estimated glomerular filtration rate (eGFR) >30 mL/min at screening.
- Participants must be willing and able to give informed consent before initiation of any study related procedures and willing to comply with all required study procedures.
Exclusion Criteria:
Participants meeting any of the following criteria are not eligible for inclusion in this study:
- Any uncontrolled or serious disease, or any medical or surgical condition, that may either interfere with participation in the clinical study and/or put the participant at significant risk (according to investigator's [or delegate] judgment) if he/she participates in the clinical study.
- An underlying known disease, or surgical, physical, or medical condition that, in the opinion of the investigator (or delegate) might interfere with interpretation of the clinical study results.
- New York Heart Association (NYHA) class IIIb or IV heart failure or last known left ventricular ejection fraction <25%.
- Significant cardiac arrhythmia within 3 months prior to randomization that is not controlled by medication or via ablation at the time of screening.
- Uncontrolled severe hypertension: systolic blood pressure >180 mmHg or diastolic blood pressure >110 mmHg prior to randomization (assessed at screening visit) despite antihypertensive therapy.
- Homozygous familial hypercholesterolemia (HoFH) defined as LDL-C ≥ 12 mmol/L.
- Statin intolerant patients defined as documented side effects on 2 different statins, including one at the lowest standard dose.
- Severe concomitant non-cardiovascular disease that carries the risk of reducing life expectancy to less than 2 years.
- History of malignancy that required surgery (excluding local and wide-local excision), radiation therapy and/or systemic therapy during the three years prior to randomization.
- Women of childbearing potential, defined as all women physiologically capable of becoming pregnant from menarche until becoming post-menopausal, unless they have had surgical bilateral oophorectomy (with or without hysterectomy), total hysterectomy or bilateral salpingectomy at least six weeks before taking study treatment. In the case of oophorectomy alone, the reproductive status of the woman needs to have been confirmed by follow-up hormone level assessment. Women are considered post-menopausal if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile (e.g., hormonal profile confirming menopause and/or age-appropriate history of vasomotor symptoms).
- Breastfeeding women.
- Treatment with other investigational products or devices within 30 days or five half-lives of the screening visit, whichever is longer.
- History of hypersensitivity to any of the study treatments or its excipients, or to drugs of similar chemical classes (statins, ezetimibe, and inclisiran).
- Planned use of other investigational products or devices during the course of the study.
Any condition that, according to the investigator, could interfere with the conduct of the study, such as but not limited to:
- Participants who are unable to communicate or to cooperate with the investigator.
- Unable to understand the protocol requirements, instructions and study-related restrictions, the nature, scope, and possible consequences of the study (including participants whose cooperation is doubtful due to drug abuse or alcohol dependency).
- Unlikely to comply with the protocol requirements, instructions, and study-related restrictions (e.g., uncooperative attitude, inability to return for follow-up visits, and improbability of completing the study).
- Persons directly involved in the conduct of the study.
- Treatment with monoclonal antibodies directed towards PCSK9 or inclisiran within 60 days of screening or planned use of it as SOC during next 210 days.
- Active liver disease defined as any known current infectious, neoplastic, or metabolic pathology of the liver or (ii) alanine aminotransferase (ALT) elevation >3x ULN, aspartate aminotransferase (AST) elevation >3x ULN, or total bilirubin elevation >2x ULN (except patients with Gilbert's syndrome) at screening confirmed by a repeat measurement at least one week apart.
- Uncontrolled Diabetes Mellitus (DM) defined as HbA1c > 9%.
Other protocol-defined inclusion/exclusion criteria may apply
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Randomizované
- Intervenční model: Paralelní přiřazení
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Experimentální: Phase 1: inclisiran + SOC
Inclisiran sodium 300 mg administered on Day 1 and Day 90 on top of standard of care (SOC)
|
Inclisiran sodium 300 mg
Ostatní jména:
consists of statins with or without ezetimibe, compared to a high-intensity SOC regimen alone (statins +/- ezetimibe)
|
|
Aktivní komparátor: Phase 1: SOC
standard of care (SOC) alone
|
consists of statins with or without ezetimibe, compared to a high-intensity SOC regimen alone (statins +/- ezetimibe)
|
|
Experimentální: Phase 2: inclisiran + SOC
Inclisiran sodium 300 mg administered on Day 90 and Day 180 for switched group (SOC alone group from first phase) on top of SOC
|
Inclisiran sodium 300 mg
Ostatní jména:
consists of statins with or without ezetimibe, compared to a high-intensity SOC regimen alone (statins +/- ezetimibe)
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Percent change in LDL-C from baseline at Day 60
Časové okno: Baseline and Day 60
|
Difference in percent change from baseline in Low-Density Lipoprotein Cholesterol (LDL-C) between inclisiran + SOC group and SOC alone group
|
Baseline and Day 60
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Absolute change from baseline in LDL-C levels
Časové okno: Baseline, Day 14, Day 30, Day 60, Day 90 in phase 1 and Day 150 in phase 2
|
Absolute change from baseline in LDL-C levels in the inclisiran + SOC group compared to SOC group at Days 14, 30, 60, 90 in phase 1 and Day 150 in all participants in phase 2
|
Baseline, Day 14, Day 30, Day 60, Day 90 in phase 1 and Day 150 in phase 2
|
|
Average percent change from baseline in LDL-C levels
Časové okno: Baseline, Day 14, Day 30, Day 60, Day 90 in phase 1 and Day 150 in phase 2
|
Average percent change from baseline in LDL-C levels in the inclisiran + SOC group compared to SOC group at Days 14, 30, 60, 90 in phase 1 and Day 150 in all participants in phase 2.
|
Baseline, Day 14, Day 30, Day 60, Day 90 in phase 1 and Day 150 in phase 2
|
|
Average absolute change from baseline in LDL-C levels
Časové okno: Baseline, Day 14, Day 30, Day 60, Day 90 in phase 1 and Day 150 in phase 2
|
Average absolute change from baseline in LDL-C levels in the inclisiran + SOC group compared to SOC group at Days 14, 30, 60, 90 in phase 1 and Day 150 in all participants in phase 2.
|
Baseline, Day 14, Day 30, Day 60, Day 90 in phase 1 and Day 150 in phase 2
|
|
Proportion of participants achieving LDL-C levels <1.4 mmol/L
Časové okno: Day 30, Day 60, Day 90 in phase 1 and Day 150 in phase 2
|
Proportion of participants achieving LDL-C levels <1.4 mmol/L in each treatment group (inclisiran + SOC vs. SOC alone) at Days 30, 60, 90 in phase 1 and Day 150 in all participants in phase 2.
|
Day 30, Day 60, Day 90 in phase 1 and Day 150 in phase 2
|
|
Proportion of participants achieving LDL-C levels <1.8 mmol/L
Časové okno: Day 30, Day 60, Day 90 in phase 1 and Day 150 in phase 2
|
Proportion of participants achieving LDL-C levels <1.8 mmol/L in each treatment group (inclisiran + SOC vs. SOC alone) at Days 30, 60, 90 in phase 1 and Day 150 in all participants in phase 2.
|
Day 30, Day 60, Day 90 in phase 1 and Day 150 in phase 2
|
|
Absolute change from baseline in VLDL, non-HDL-C, TC, HDL-C and TG
Časové okno: Baseline and Day 90
|
Absolute change from baseline in very low-density lipoprotein (VLDL), non-high-density lipoprotein cholesterol (non-HDL-C), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C) and triglycerides (TG) in the inclisiran + SOC group compared to the SOC group at Day 90 in phase 1
|
Baseline and Day 90
|
|
Absolute change from baseline in Lp(a)
Časové okno: Baseline and Day 90
|
Absolute change from baseline in lipoprotein(a) (Lp(a)) in the inclisiran + SOC group compared to the SOC group at Day 90 in phase 1
|
Baseline and Day 90
|
|
Proportion of participants needing additional lipid lowering therapy
Časové okno: Day 90 in phase 1 and Day 150 in phase 2
|
Proportion of participants needing additional lipid lowering therapy in the inclisiran + SOC group compared to the SOC group at Day 90 in phase 1 and Day 150 in all participants in phase 2.
|
Day 90 in phase 1 and Day 150 in phase 2
|
|
Average percent change in LDL-C levels
Časové okno: Between Day 30 and Day 90 in phase 1 and Day 150 in phase 2
|
Average percent change in LDL-C levels in the inclisiran + SOC group compared to the SOC group between Day 30 and Day 90 in phase 1 and Day 150 in all participants in phase 2
|
Between Day 30 and Day 90 in phase 1 and Day 150 in phase 2
|
|
Average absolute change in LDL-C levels
Časové okno: Between Day 30 and Day 90 in phase 1 and Day 150 in phase 2
|
Average absolute change in LDL-C levels in the inclisiran + SOC group compared to the SOC group between Day 30 and Day 90 in phase 1 and Day 150 in all participants in phase 2.
|
Between Day 30 and Day 90 in phase 1 and Day 150 in phase 2
|
|
Proportion of participants achieving a target LDL-C level <1.4 mmol/L
Časové okno: Day 210
|
Proportion of participants achieving a target LDL-C level <1.4 mmol/L in all participants in Phase 2 at Day 210.
|
Day 210
|
|
Proportion of participants achieving a target LDL-C level <1.8 mmol/L
Časové okno: Day 210
|
Proportion of participants achieving a target LDL-C level <1.8 mmol/L in all participants in Phase 2 at Day 210.
|
Day 210
|
|
Average percent change from baseline in LDL-C levels
Časové okno: Day 210
|
Average percent change from baseline in LDL-C levels in all participants in Phase 2 at Day 210.
|
Day 210
|
|
Average absolute change from baseline in LDL-C levels
Časové okno: Day 210
|
Average absolute change from baseline in LDL-C levels in all participants in Phase 2 at Day 210
|
Day 210
|
|
Number of participants with AEs and SAEs
Časové okno: Up to 210 days
|
Number of participants with adverse events (AEs), serious adverse events (SAEs), including abnormal values in hematology evaluation, blood chemistry and urine, vital signs, and physical examinations.
|
Up to 210 days
|
|
Mean score in the Treatment Satisfaction Questionnaire for Medication (TSQMII)
Časové okno: Day 210
|
The Treatment Satisfaction Questionnaire about Medication (TSQMII) version II is a validated 11 item scale which, in this study, will assess a patients' satisfaction (with regard to their lipid lowering treatments), providing scores on four scales: 1) side effects, 2) effectiveness, 3) convenience and 4) global, overall, satisfaction. TSQMII assesses patients' satisfaction with medication with a higher score, reflecting greater overall satisfaction (1=extremely dissatisfied and 7=extremely satisfied) |
Day 210
|
Spolupracovníci a vyšetřovatelé
Sponzor
Vyšetřovatelé
- Ředitel studie: Novartis Pharmaceuticals, Novartis Pharmaceuticals
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
- CKJX839A1SA03
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Popis plánu IPD
Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations.
This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com
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 .
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