drugset / Trial / NCT03194776

Study of LLG783 in Patients With Peripheral Artery Disease (PAD) and Intermittent Claudication

NCT03194776 ↗

Phase 2 Completed 46 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is designed to determine whether LLG783 displays the clinical safety and efficacy profile, after multiple i.v. doses, to support further development in patients with PAD and intermittent claudication.

Timeline

Start
2017-09-20
Primary completion
2018-09-07
Completion
2018-12-27

Outcome

Missed primary endpoint

registry analysis (superiority test); LLG783 6mg/kg vs Placebo; p = 0.2612; Mean Difference (Final Values) -17.74 NCT03194776 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject LLG783 Unknown — Intravenous