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Active Not Recruiting NCT06275724

Specified Drug-use Survey of Leqvio for s.c. Injection.

Conditions: Familial Hypercholesterolaemia, Hypercholesterolaemia

Sex: All
Ages: 15 Years – 100 Years
Healthy volunteers: No
Enrollment: 585
Sponsor: Novartis Pharmaceuticals

Location: Novartis Investigative Site Handa Aichi-ken

Summary

The objective of this study is to evaluate the long-term safety of Leqvio in patients with familial hypercholesterolaemia or hypercholesterolaemia in post-marketing clinical practice

Eligibility Criteria

Inclusion Criteria: * Patients who provided written informed consent to participate in this survey prior to the start of treatment with Leqvio. * Patients who received treatment with Leqvio as per the package insert. Exclusion Criteria: * Patients who received treatment with a formulation containing the same ingredients as Leqvio in the past. * Patients participating in other interventional studies at the time of informed consent. * Patients planning to participate in other interventional studies during this survey.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT06275724). StuddyBuddy aggregates publicly available trial information.