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Resverlogix Corp T.RVX

Alternate Symbol(s):  RVXCF

Resverlogix Corp. is a Canada-based late-stage biotechnology company. The Company is engaged in epigenetics, with a focus on developing therapies for the benefit of patients with chronic diseases. Its epigenetic therapies are designed to regulate the expression of disease-causing genes. The Company's clinical program is focused on evaluating its lead candidate apabetalone (RVX-208) for the treatment of cardiovascular disease and associated comorbidities, and post-COVID-19 conditions. RVX-208 is a small molecule that is a selective bromodomain and extra-terminal (BET) inhibitor. BET bromodomain inhibition is an epigenetic mechanism that can regulate disease-causing genes. RVX-208 is a BET inhibitor selective for the second bromodomain (BD2) within the BET proteins. It partners with EVERSANA, to support the commercialization of RVX-208 for cardiovascular disease, post-COVID-19 conditions, and pulmonary arterial hypertension in Canada and the United States.


TSX:RVX - Post by User

Bullboard Posts
Post by priceless2on Dec 05, 2016 12:35pm
106 Views
Post# 25555345

DSBM 2nd postive recommendation

DSBM 2nd postive recommendationhttps://finance.yahoo.com/news/resverlogix-announces-second-positive-recommendation-171300385.html

CALGARY , Dec. 5, 2016 /CNW/ - Resverlogix Corp. ("Resverlogix" or the "Company") (RVX.TO) today announced that the independent Data and Safety Monitoring Board (DSMB) for the Company's Phase 3 BETonMACE trial in high-risk cardiovascular disease (CVD) patients has completed a second planned safety review and recommended that the study should continue as planned without any modifications. The DSMB reviewed available study data and noted that no safety or efficacy concerns were identified. The DSMB will conduct additional periodic reviews and will also perform a futility assessment once 125 adjudicated major adverse cardiac events (MACE) have been observed. Resverlogix, the clinical steering committee, and all investigators remain blinded to the actual safety and efficacy results.

"This second review and recommendation of the DSMB to continue as planned in the BETonMACE trial is clearly encouraging. The first patients in the trial have now surpassed the one year mark and apabetalone remains well-tolerated with a consistent safety profile." stated Dr. Michael Sweeney , M.D., Senior Vice President of Clinical Development. "We look forward to reporting additional updates."

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