← Back to all trials
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.
Source: ClinicalTrials.gov (NCT06275724). StuddyBuddy aggregates publicly available trial information.