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Study identifier: NCT07626281 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Assessment of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of a New Formulation of Inclisiran Containing Polysorbate 80 Compared to the Currently Marketed Formulation

Condition: Inclisiran Formulation  ·  Sponsor: Novartis Pharmaceuticals

PhasePhase 1
Planned participants120
Who can joinAll sexes, 18 Years to 60 Years
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Novartis Pharmaceuticals  ·  1-888-669-6682  ·  novartis.email@novartis.com

Novartis Pharmaceuticals

Always discuss trial participation with your own doctor first.

Locations (3)

Lenexa Research UnitLenexa, Kansas, United StatesRecruiting
Cardiovasular Renal MetabolismSan Antonio, Texas, United StatesRecruiting
Salt Lake City Research UnitSalt Lake City, Utah, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07626281