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NCT05399992Active, not recruiting

Study Evaluating LDL-C Change and Adherence to Inclisiran Lipid-lowering Therapy in ASCVD

VICTORION REAL: An International Prospective Real-world Study to Evaluate the LDL-C changE and Adherence to incLisiran in Participants With Primary Hypercholesterolemia or Mixed Dyslipidemia

Source: ClinicalTrials.gov · Last updated 24 Sept 2026

Brief summary (registry, in English)

This observational prospective study aims to evaluate the LDL-C change and adherence to inclisiran in combination with other lipid lowering therapies or lipid lowering treatments (LLTs) under conditions of routine clinical practice.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
847 (actual)
First submitted
27 May 2022
Start date
12 Sept 2022
Primary completion date
5 Oct 2026
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT05399992

What you commit to

  • Study type: Observational
  • Participants enrolled: 847
  • From 12 Sept 2022 to the primary completion date, 5 Oct 2026
  • 34 sites in 8 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participants that have received inclisiran previously
  • Participants participating in a clinical trial with investigational product 3 Participants switching from previous PCSK9 mab treatment (within 90 days prior to Index date)

Who the study is looking for

  • Participants who are 18 years or older
  • Participants with hypercholesterolemia having a diagnosis of ASCVD, ASCVD RE or HeFH
  • Participants who are not at LDL-C goal as per their CV risk according to respective clinical guidelines
  • Participants who per physician's criteria need to optimize their LLT
  • Participants who provide written informed consent to participate in the study
  • Participants who initiate inclisiran under conditions per local label and have LDL-C values available at baseline or within 3 months before treatment initiation.

Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (34)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Novartis Investigative Site
Coordinator of this site? Confirm its status
Abu DhabiUnited Arab EmiratesUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
Al Ain CityUnited Arab EmiratesUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
DubaiUnited Arab EmiratesUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
FeldkirchAustriaUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
GrazAustriaUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
LinzAustriaUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
Sankt Veit im PongauAustriaUnknown status
Novartis Investigative Site
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ViennaAustriaUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
BaselSwitzerlandUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
FribourgSwitzerlandUnknown status
Novartis Investigative Site
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GenevaSwitzerlandUnknown status
Novartis Investigative Site
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LausanneSwitzerlandUnknown status
Novartis Investigative Site
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OltenSwitzerlandUnknown status
Novartis Investigative Site
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Sankt GallenSwitzerlandUnknown status
Novartis Investigative Site
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ZurichSwitzerlandUnknown status
Novartis Investigative Site
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ShenzhenChinaUnknown status
Novartis Investigative Site
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BelfastUnited KingdomUnknown status
Novartis Investigative Site
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BromwichUnited KingdomUnknown status
Novartis Investigative Site
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Burton-on-TrentUnited KingdomUnknown status
Novartis Investigative Site
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High WycombeUnited KingdomUnknown status
Novartis Investigative Site
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HullUnited KingdomUnknown status
Novartis Investigative Site
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LancasterUnited KingdomUnknown status
Novartis Investigative Site
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LiverpoolUnited KingdomUnknown status
Novartis Investigative Site
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LondonUnited KingdomUnknown status
Novartis Investigative Site
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LouthUnited KingdomUnknown status
Novartis Investigative Site
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MiddlesexUnited KingdomUnknown status
Novartis Investigative Site
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SunderlandUnited KingdomUnknown status
Novartis Investigative Site
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HolonIsraelUnknown status
Novartis Investigative Site
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Petah TikvaIsraelUnknown status
Novartis Investigative Site
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Tel AvivIsraelUnknown status
Novartis Investigative Site
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Kuala LumpurMalaysiaUnknown status
Novartis Investigative Site
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JeddahSaudi ArabiaUnknown status
Novartis Investigative Site
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RiyadhSaudi ArabiaUnknown status
Novartis Investigative Site
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TabukSaudi ArabiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.