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Adherence and Persistence to Inclisiran Among Early Users in Germany

Adherence and Persistence to Inclisiran Among Early Users in Germany

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05870657
Enrollment
1109
Registered
2023-05-23
Start date
2022-02-16
Completion date
2022-05-12
Last updated
2023-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High Levels of Low-density Lipoprotein Cholesterol

Brief summary

The present study was a descriptive, non-interventional, retrospective cohort study aimed at evaluating early data on adherence, persistence, and treatment patterns among patients receiving inclisiran and other lipid-lowering therapies (LLT) in a real-world setting in Germany. Analysis was carried out using the IQVIA™ LRx database.

Interventions

None listed

Sponsors

Novartis Pharmaceuticals
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Study subjects ≥18 years old who were prescribed an inclisiran dose.

Exclusion criteria

None

Design outcomes

Primary

MeasureTime frame
Number and percentage of patients with at least 5 months of potential follow-up who were prescribed a second dose of inclisiran8 months
Percentage of patients who were prescribed a second dose of inclisiran between 1 and 6 months after prescription of first dose8 months
Median time between first and second prescribed doses8 months

Secondary

MeasureTime frame
Age and gender characteristics6 months
Age and gender distribution6 months
Prescriber specialty distribution for patients6 months

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026