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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

29 giugno 2026 aggiornato da: Novartis Pharmaceuticals

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

This study aims to evaluate the effectiveness and safety of implementing a systematic augmented low-density lipoprotein cholesterol (LDL-C) management care pathway initiated in hospitals for patients with Acute Coronary Syndrome. This pathway includes treatment with inclisiran on top of the standard of care (SOC), which consists of statins with or without ezetimibe, compared to a high-intensity SOC regimen alone (statins +/- ezetimibe).

Panoramica dello studio

Stato

Non ancora reclutamento

Intervento / Trattamento

Descrizione dettagliata

This multi-center phase IV study adopted a two-phase design. The first phase (Day 1 to Day 90) is an open-label, randomized, comparative parallel-group design comparing an LDL-C management strategy that includes inclisiran with SOC versus SOC alone. The second phase is an open-label extension design (Day 90 to Day 210). After the EOI visit, the participants from phase 2 will be invited to participate in a 1-year long-term observational phase to assess medication adherence and satisfaction.

Tipo di studio

Interventistico

Iscrizione (Stimato)

300

Fase

  • Fase 4

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

  • Nome: Novartis Pharmaceuticals

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

Participants eligible for inclusion in this study must meet all of the following criteria:

  1. Males and females ≥18 years of age.
  2. Recent ACS (in-patient/out-patient) within 7 days of index admission, as per 2023 ESC guidelines for the management of acute coronary syndrome
  3. 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.
  4. 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.
  5. Fasting triglycerides <4.52 mmol/L (<400 mg/dL) at screening.
  6. Estimated glomerular filtration rate (eGFR) >30 mL/min at screening.
  7. 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:

  1. 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.
  2. 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.
  3. New York Heart Association (NYHA) class IIIb or IV heart failure or last known left ventricular ejection fraction <25%.
  4. Significant cardiac arrhythmia within 3 months prior to randomization that is not controlled by medication or via ablation at the time of screening.
  5. Uncontrolled severe hypertension: systolic blood pressure >180 mmHg or diastolic blood pressure >110 mmHg prior to randomization (assessed at screening visit) despite antihypertensive therapy.
  6. Homozygous familial hypercholesterolemia (HoFH) defined as LDL-C ≥ 12 mmol/L.
  7. Statin intolerant patients defined as documented side effects on 2 different statins, including one at the lowest standard dose.
  8. Severe concomitant non-cardiovascular disease that carries the risk of reducing life expectancy to less than 2 years.
  9. 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.
  10. 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).
  11. Breastfeeding women.
  12. Treatment with other investigational products or devices within 30 days or five half-lives of the screening visit, whichever is longer.
  13. History of hypersensitivity to any of the study treatments or its excipients, or to drugs of similar chemical classes (statins, ezetimibe, and inclisiran).
  14. Planned use of other investigational products or devices during the course of the study.
  15. Any condition that, according to the investigator, could interfere with the conduct of the study, such as but not limited to:

    1. Participants who are unable to communicate or to cooperate with the investigator.
    2. 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).
    3. 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).
    4. Persons directly involved in the conduct of the study.
  16. 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.
  17. 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.
  18. Uncontrolled Diabetes Mellitus (DM) defined as HbA1c > 9%.

Other protocol-defined inclusion/exclusion criteria may apply

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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
Altri nomi:
  • KJX839
consists of statins with or without ezetimibe, compared to a high-intensity SOC regimen alone (statins +/- ezetimibe)
Comparatore attivo: 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)
Sperimentale: 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
Altri nomi:
  • KJX839
consists of statins with or without ezetimibe, compared to a high-intensity SOC regimen alone (statins +/- ezetimibe)

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Percent change in LDL-C from baseline at Day 60
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Absolute change from baseline in LDL-C levels
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Direttore dello studio: Novartis Pharmaceuticals, Novartis Pharmaceuticals

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

30 giugno 2026

Completamento primario (Stimato)

28 febbraio 2027

Completamento dello studio (Stimato)

31 ottobre 2028

Date di iscrizione allo studio

Primo inviato

29 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

29 giugno 2026

Primo Inserito (Effettivo)

6 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

29 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

Descrizione del piano 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

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Sindrome coronarica acuta

Prove cliniche su inclisiran

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