drugset / Trial / NCT03466203

Safety Study of LLF580 in Obese Volunteers

NCT03466203 ↗

Phase 1 Completed 61 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of the study is to evaluate the safety and tolerability of multiple doses of LLF580 administered subcutaneously over 3 months in obese subjects. In addition, the study will also determine early efficacy signals in various metabolic diseases associated with elevated triglycerides and/or obesity.

Timeline

Start
2018-02-26
Primary completion
2019-11-13
Completion
2019-11-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Efimosfermin alfa Unknown 300 mg Subcutaneous

Indications