Apabetalone Treatment Prevents COVID-19 Infection of Human Lung Cells

Apabetalone Inhibits SARS-CoV-2 Infection at Levels Comparable to Approved Antiviral

CALGARY, Alberta, March 15, 2021 (GLOBE NEWSWIRE) -- Resverlogix Corp. ("Resverlogix") (TSX:RVX) announced today the publishing of a new article titled: “Bromodomain and extraterminal protein inhibitor, apabetalone (RVX-208), reduces ACE2 expression and attenuates SARS-CoV-2 infection in vitro”, on the pre-print server, bioRxiv. The findings, made in collaboration with Dr. Dalia ElGamal’s research group at the University of Nebraska Medical Center (UNMC), Omaha, NE, provide a strong rationale for use of apabetalone, a bromodomain and extraterminal (BET) protein inhibitor, as a therapeutic for COVID-19.

The publication can be viewed using the following LINK.

“Our COVID-19 research program has yielded some truly extraordinary results, demonstrating apabetalone’s ability to prevent SARS-CoV-2 infection of human lung cells,” said Dr. Ewelina Kulikowski, Senior Vice President, Research & Development at Resverlogix. “Reducing cellular entry of virus particles into the lung tissue is one pillar of apabetalone’s unique dual-mechanism – alongside inhibiting damaging inflammation – in combatting COVID-19.”

“This work would not have been possible without the invaluable contribution of Dr. ElGamal and colleagues at UNMC,” said Donald McCaffrey, President and CEO of Resverlogix. “We are grateful to work with world-class scientific leaders to characterize apabetalone as a therapeutic for COVID-19 infection for the future benefit of patients.”

“Together with St. Patrick Reid, a prominent virologist at UNMC who's lab is dedicated to molecular pathogenesis of emerging viral pathogens, we found that apabetalone clearly inhibited SARS-CoV-2 infection of human lung epithelial cells,” said Dr. Dalia ElGamal, co-author and Assistant Professor at the Eppley Institute for Research in Cancer and Allied Diseases at UNMC. “Given apabetalone’s anti-inflammatory properties, and its favorable safety profile in human trails, I am excited to see apabetalone move forward in clinical trials for COVID-19.”

Publication Highlights include:

• Angiotensin-converting enzyme 2 (ACE2) and dipeptidyl-peptidase 4 (DPP4) are key proteins used by SARS-CoV-2 to gain entry into human cells
• Treatment with apabetalone reduces the expression of both ACE2 and DPP4 at the surface of human lung epithelial cells
• Viral spike proteins, which bind ACE2 and initiate cell entry, adhere significantly less to apabetalone treated cells than control cells
• Apabetalone prevents human SARS-CoV-2 infection of human lung epithelial cells at comparable levels to the antivirals remdesivir – a currently approved treatment for COVID-19 by the US Food and Drug Administration - and camostat mesylate
• Cell viability is not impacted by drug treatment, the authors also note apabetalone’s well-established safety record in patients
• Apabetalone’s observed dual mechanism of action on viral infection and inflammation support the use of apabetalone in clinical trials for COVID-19.

Program Update: