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BOLD-100 MoA Research to Be Presented at the AACR Annual Meeting


Queen s University Belfast, Northern Ireland
Van Schaeybroeck s AACR poster presentation Targeting the DNA repair pathway with BOLD-100 in BRAF-mutant colorectal cancer (Poster# 1183, Session PO.ET04.03 on April 10) highlights the promising research conducted by the Drug Resistance Group at the Patrick G. Johnston Centre for Cancer Research at Queen s University Belfast, which investigated BOLD-100 s mechanism-of-action and identified promising treatment combinations in difficult-to-treat BRAF-mutant colorectal cancers.
Colon cancer is one of the most frequently diagnosed malignancies in adults, responsible for approximately 11% of all new cases of cancers worldwide and one-third of cancer deaths. BRAF-mutant colorectal cancers comprise 10% of those patients, and this subgroup has morphological, clinical, and therapeutic characteristics that differ substantially from patients without this genetic alteration. Importantly, there is no established standard of care for BRAF- ....

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Bold Therapeutics Secures Funding to Prepare BOLD-100 for COVID-19 Clinical Trials


COVID-19 cases continue to escalate worldwide
The original announcement by the National Research Council of Canada is available at bit.ly/2JRa4fQ.
BOLD-100 is a first-in-class ruthenium-based small molecule drug which selectively inhibits stress-induced upregulation of the chaperone protein GRP78. Currently, the investigational treatment is in a Phase 1b clinical trial in gastrointestinal cancer. 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. Preclinical studies have repeatedly demonstrated BOLD-100 has a robust antiviral response against COVID-19.
We are thankful to have this support from NRC IRAP to continue developing BOLD-100 as an antiviral stated Mark Bazett, PhD, Director of Preclinical Development of Bold Therapeutics. We look forward to completing the next required set of nonclinical and manufacturing studies so ....

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