- ICH GCP
- US-Register für klinische Studien
- Klinische 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
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Studientyp
Einschreibung (Geschätzt)
Phase
- Phase 4
Kontakte und Standorte
Studienkontakt
- Name: Novartis Pharmaceuticals
- Telefonnummer: +41613241111
- E-Mail: novartis.email@novartis.com
Studieren Sie die Kontaktsicherung
- Name: Novartis Pharmaceuticals
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: 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
Andere Namen:
consists of statins with or without ezetimibe, compared to a high-intensity SOC regimen alone (statins +/- ezetimibe)
|
|
Aktiver Komparator: 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)
|
|
Experimental: 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
Andere Namen:
consists of statins with or without ezetimibe, compared to a high-intensity SOC regimen alone (statins +/- ezetimibe)
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Percent change in LDL-C from baseline at Day 60
Zeitfenster: 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
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Absolute change from baseline in LDL-C levels
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Studienleiter: Novartis Pharmaceuticals, Novartis Pharmaceuticals
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- CKJX839A1SA03
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
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
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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