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Assessment of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of a New Formulation of Inclisiran Containing Polysorbate 80 Compared to the Currently Marketed Formulation
Sponsor: Novartis Pharmaceuticals
Summary
The purpose of this study is to compare safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of the currently marketed formulation of inclisiran with a new formulation containing polysorbate 80 (PS80), after a single 284 mg subcutaneous (SC) administration.
Official title: A Randomized, Open-label, Single-dose, Parallel-group Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Inclisiran Containing Polysorbate 80 Versus Inclisiran Alone in Participants With Elevated Low-density Lipoprotein Cholesterol
Key Details
Gender
All
Age Range
18 Years - 60 Years
Study Type
INTERVENTIONAL
Enrollment
120
Start Date
2026-06-09
Completion Date
2026-12-21
Last Updated
2026-07-10
Healthy Volunteers
Yes
Conditions
Interventions
Inclisiran formulation containing PS80
Inclisiran 284 mg
Currently marketed inclisiran formulation
Inclisiran 284 mg
Locations (3)
Lenexa Research Unit
Lenexa, Kansas, United States
Cardiovasular Renal Metabolism
San Antonio, Texas, United States
Salt Lake City Research Unit
Salt Lake City, Utah, United States