Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CSL112 is an investigational intravenous infusion therapy consisting of purified human plasma-derived apolipoprotein A-I (apoA-I) reconstituted with phosphatidylcholine into disc-shaped high-density lipoprotein (HDL) particles. Developed by CSL for the treatment of acute myocardial infarction (AMI), its primary mechanism is to rapidly enhance cholesterol efflux capacity from macrophages in atherosclerotic plaques via ABCA1-dependent and independent pathways. This process increases pre-beta HDL levels and promotes reverse cholesterol transport to the liver for clearance. In addition to promoting cholesterol efflux, it may exert anti-inflammatory effects that help stabilize vulnerable atherosclerotic plaques during the high-risk period following AMI. Unlike recombinant or mimetic agents, the apoA-I in CSL112 is purified from human plasma[1][3][4][6].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on CSL112.