Publications! See pages 23-24 of Annual Information Form, also copied below.
We already knew about the first one below. But one more has been accepted with revision and two more have been submitted, including the long awaited BETonMACE trial design and rationale paper!
I am very impressed by the volume of research that Resverlogix and collaborators have been publishing over the years. So much informative published on apabetalone research.
- "A manuscript titled “Apabetalone (RVX-208) reduces vascular inflammation in vitro and in CVD patients by a BET-dependent epigenetic mechanism” was recently accepted by Clinical Epigenetics (In Press). This publication highlights the effects of apabetalone treatment on markers of vascular inflammation and cellular adhesion in vitro and in clinical plasma samples, as well as showing a reduction of monocyte adhesion to endothelial cells in cell models, with additional data supporting the BET dependent nature of these processes.
- Currently, an additional manuscript has been accepted with revisions to the Journal of Translational Medicine, titled “Epigenetic modulation by apabetalone counters cytokine driven acute phase response in vitro, in mice and in cardiovascular disease patients”. This work compiles all findings to date regarding apabetalone’s effects on the acute phase response, related targets and pathways.
- A manuscript has been submitted to the American Heart Journal titled “Effect of selective BET protein inhibitor apabetalone on cardiovascular outcomes in patients with acute coronary syndrome and diabetes: Rationale, design, and baseline characteristics of the BETonMACE trial” outlining details of BETonMACE study design and patient characteristics collected at enrollment.
- We have submitted a manuscript titled “Apabetalone Lowers Serum Alkaline Phosphatase and Improves Cardiovascular Risk in Patients with Cardiovascular Disease”, led and written in collaboration with clinical experts in the area ALP and CKD, This publication has been re-submitted with requested edits to Atheroslcerosis. Data contained in this manuscript highlights the role of ALP in cardiovascular risk, and the benefits of apabetalone induced reduction of ALP in reducing cardiovascular risk in treated CVD patients."