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ACTIVE NOT RECRUITING
NCT05726838

The Belgian REAL (BE.REAL) Registry

Sponsor: Novartis Pharmaceuticals

View on ClinicalTrials.gov

Summary

This is an observational non-interventional study. The visit schedule is according to the routine clinical practice. Only data corresponding to study variables within the specified study period will be collected. The study will recruit patients into one single cohort: Inclisiran in combination with other LLTs. The patients will receive Inclisiran therapy as per the approved label and Belgian reimbursement conditions.

Official title: A Belgian Registry to Evaluate the Real Life Treatment With Inclisiran on Top of Standard of Care Lipid-lowering Therapy in Patients With Atherosclerotic Cardiovascular Disease

Key Details

Gender

All

Age Range

18 Years - 99 Years

Study Type

OBSERVATIONAL

Enrollment

600

Start Date

2022-04-15

Completion Date

2029-03-30

Last Updated

2026-03-12

Healthy Volunteers

No

Interventions

OTHER

Inclisiran

There is no treatment allocation. Patients administered inclisiran by prescription will be enrolled. The patients will receive inclisiran therapy as per the approved label and Belgian reimbursement conditions.

Locations (15)

Novartis Investigative Site

Turnhout, Antwerpen, Belgium

Novartis Investigative Site

Genk, Limburg, Belgium

Novartis Investigative Site

Yvoir, Namur, Belgium

Novartis Investigative Site

Leuven, Vlaams Brabant, Belgium

Novartis Investigative Site

Kortrijk, West-Vlaanderen, Belgium

Novartis Investigative Site

Aalst, Belgium

Novartis Investigative Site

Anderlecht, Belgium

Novartis Investigative Site

Brasschaat, Belgium

Novartis Investigative Site

Brussels, Belgium

Novartis Investigative Site

Edegem, Belgium

Novartis Investigative Site

Ghent, Belgium

Novartis Investigative Site

Haine-Saint-Paul, Belgium

Novartis Investigative Site

Huy, Belgium

Novartis Investigative Site

Liège, Belgium

Novartis Investigative Site

Mechelen, Belgium