Drug Candidate Significantly Outperforms Gilead’s Remdesivir Head-to-Head in SARS-CoV-2 (COVID-19) Model

By HospiMedica International staff writers
Posted on 20 Aug 2020
In a series of experiments in which a first-in-class ruthenium-based small molecule drug and Gilead Sciences’ (Foster City, CA, USA) remdesivir were tested head-to-head in a cytopathic effect assay against a live Wuhan strain of SARS-CoV-2 in Vero E6 cells, the new drug candidate clearly demonstrated its efficacy as a highly potent antiviral agent.

The new drug candidate, BOLD-100, developed by Bold Therapeutics, Inc. (Vancouver, BC, Canada), showed low nanomolar IC50 values, a magnitude lower (1/10th) than the IC50 values of remdesivir, the only currently approved therapeutic for COVID-19. BOLD-100 selectively inhibits stress-induced upregulation of the chaperone protein GRP78. In cancer, GRP78 plays a critical role in resistance, survival and proliferation, whereas in viral infections, GRP78 plays a critical role in host recognition, viral entry and viral replication. BOLD-100 has the potential to substantially reduce severity of infection, shortening hospital stays and reducing morbidity and mortality. Most importantly, BOLD-100 could be effective against not just the current pandemic, but also future viral pandemics.

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Bold Therapeutics has already manufactured more than sufficient drug product to support immediate clinical studies in COVID-19 due to an ongoing Phase 1/2 trial of BOLD-100 in combination with FOLFOX in the treatment of advanced GI cancers, with an open IND with the US FDA and a February 2020 NOL from Health Canada. In an earlier Phase 1 dose-escalation study of 46 patients with advanced cancer, BOLD-100 was safe and well-tolerated, potentially allowing BOLD-100 to move immediately into Phase 2 trials in COVID-19. These factors allow BOLD-100 to be developed and potentially approved as an anti-COVID-19 therapeutic in a relevant timeframe, rather than years from now.

“Bold Therapeutics’ ongoing collaboration with some of the top virologists in Canada continues to produce independent data supporting BOLD-100 as a novel antiviral,” said Dr. Mark Bazett, Bold Therapeutics’ Director of Preclinical Development. “Today’s data is particularly impressive, showing that BOLD-100 is substantially more potent as an antiviral than remdesivir, the only recently Health Canada approved treatment for COVID-19. The collective evidence on BOLD-100 supports further, rapid development of this novel treatment option to support patients with COVID-19.”

Related Links:

Bold Therapeutics, Inc.
Gilead Sciences

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