CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 189 enrolled
Drug / intervention
ACZ885 +1 moredrug
Likely dose
ACZ885 150 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00995930
NCT00995930Phase 2Completed

A Multi-center, Randomized , Double Blind, Placebo-controlled, Study of the Safety, Tolerability, and Effects on Arterial Structure and Function of ACZ885 in Patients With Clinically Evident Atherosclerosis and Either T2DM or IGT

Novartis Pharmaceuticals·interventional·Posted Oct 16, 2009·Updated Jun 29, 2015

In Brief

A Phase 2 clinical trial evaluating ACZ885 and Placebo for Diabetes Mellitus, Type 2 and 2 related conditions. Completed, enrolled 189 participants across 9 sites in 5 countries.

Detailed Summary

This study will evaluate the effect of ACZ885 on vascular function in patients with documented atherosclerotic disease and T2DM or IGT.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, Germany, Israel, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedOct 16, 2009
Enrollment StartDec 1, 2009
Primary CompletionFeb 1, 2014
TodayJul 2, 2026
Enrollment to primary: 4.2 yearsPosted 16.7 years ago

Interventions

ACZ885drug

ACZ885 150 mg was administered subcutaneously once a month for 12 months.

Placebodrug

Matching placebo to ACZ885 was administered subcutaneously once a month for 12 months.