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RECRUITING
NCT07626281
PHASE1

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

View on ClinicalTrials.gov

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

Interventions

DRUG

Inclisiran formulation containing PS80

Inclisiran 284 mg

DRUG

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