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Study to Investigate CSL112 in Subjects With Acute Coronary Syndrome

Completed · Phase 3 · NCT03473223

Conditions: Acute Coronary Syndrome

At a glance

Research payments reported, 2025
$429,636
U.S. investigators named
5
Sites paid
5
Planned or actual enrollment
18,226

About the trial

Sponsor
CSL Behring
Tested
Apolipoprotein A-I [human] (apoA-I) (biological), Placebo (other)
Dates
Started 2018-03-21; completion 2023-11-17
Results posted
Yes

This is a phase 3, multicenter, double-blind, randomized, placebo-controlled, parallel-group study to evaluate the efficacy and safety of CSL112 on reducing the risk of major adverse CV events \[MACE - cardiovascular (CV) death, myocardial infarction (MI), and stroke\] in subjects with acute coronary syndrome (ACS) diagnosed with either ST-segment elevation myocardial infarction (STEMI) or non-ST-segment elevation myocardial infarction (NSTEMI), including those managed with percutaneous coronary intervention (PCI) or medically managed.

From ClinicalTrials.gov, last updated 2025-01-14. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Csl Behring reported $429,636 in research payments for this study in 2025 (7 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.