drugset / Trial / NCT06132360

the Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamic Effects in Adult Subjects With Elevated LDL-C

NCT06132360 ↗

Phase 1 Completed 32 enrolled Shanghai Rona Therapeutics Co., Ltd.
RandomizedSequentialSingle-blindTreatment

Summary

This is a randomized, placebo-controlled, single ascending-dose (SAD) study of administered SC to adult subjects with elevated LDL-C. Subjects who have signed an Ethics Committee (EC)-approved informed consent form (ICF) and have met all the protocol eligibility criteria during screening may be enrolled into the study.

Timeline

Start
2024-01-18
Primary completion
2024-07-02
Completion
2024-09-23

Drugs

EvaluationDrugModalityDoseRoute
Subject RN0191 Unknown — Subcutaneous