Exclusive Rights to Cas12 and Cas13 Maintains Sherlock Biosciences as Leading CRISPR Diagnostic Manufacturer, While Providing Partners with the Most Comprehensive Portfolio of Diagnostic CRISPR Enzymes
December 04, 2020 08:30 AM Eastern Standard Time
CAMBRIDGE, Mass.--(BUSINESS WIRE)--Sherlock Biosciences, an Engineering Biology company dedicated to making diagnostic testing better, faster and more affordable, today announced exclusive license agreements with Shanghai-based Tolo Biotech. Tolo has granted Sherlock exclusive rights in the United States to its CRISPR-Cas12 (including Cas12a and Cas12b) diagnostic technology, and Sherlock has granted Tolo exclusive rights to the CRISPR-Cas13 SHERLOCK™ diagnostic platform in Greater China. Financial details have not been disclosed.“We are very pleased to enter this agreement with Tolo, which complements Sherlock’s diagnostic rights to the Cas12 and Cas13 proteins licensed from the Broad Institute,” said Rahul Dhanda, co-founder, president and CEO of Sherlock Biosciences. “With the addition of these exclusive Cas12 rights to Sherlock’s IP portfolio, as well as partnering with Tolo as our exclusive partner in China, we have secured our position as the global leader in CRISPR diagnostics.”"The advent of CRISPR technology is ushering in the next generation of molecular diagnostics,” said Jin Wang, co-founder and chief science officer of Tolo Biotech. “This agreement with Sherlock will enable both companies to develop diagnostic tools that can detect multiple pathogens or targets, improving disease screening, precision medicine and beyond. Tolo highly values this opportunity for close collaboration with Sherlock to promote the development of CRISPR diagnostics.”The SHERLOCK diagnostic platform can achieve single molecule detection of nucleic acid targets; its name stands for Specific High Sensitivity Enzymatic Reporter unLOCKing. SHERLOCK utilizes CRISPR activity for “smart amplicon detection” and can be adapted for use with existing diagnostic instruments, improving time to result due to its significant multiplexing capacity. When a specific sequence of DNA or RNA is present, a CRISPR enzyme is activated and, much like a pair of scissors, starts cutting nearby genetic material, releasing a fluorescent signal that indicates a positive result. In May 2020, Sherlock received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for its Sherlock™ CRISPR SARS-CoV-2 kit, the first FDA-authorized use of CRISPR technology.
Exclusive Rights to Cas12 and Cas13 Maintains Sherlock Biosciences as Leading CRISPR Diagnostic Manufacturer, While Providing Partners with the Most Comprehensive Portfolio of Diagnostic CRISPR Enzymes
December 04, 2020 08:30 AM Eastern Standard Time
CAMBRIDGE, Mass.--(BUSINESS WIRE)--Sherlock Biosciences, an Engineering Biology company dedicated to making diagnostic testing better, faster and more affordable, today announced exclusive license agreements with Shanghai-based Tolo Biotech. Tolo has granted Sherlock exclusive rights in the United States to its CRISPR-Cas12 (including Cas12a and Cas12b) diagnostic technology, and Sherlock has granted Tolo exclusive rights to the CRISPR-Cas13 SHERLOCK™ diagnostic platform in Greater China. Financial details have not been disclosed.“We are very pleased to enter this agreement with Tolo, which complements Sherlock’s diagnostic rights to the Cas12 and Cas13 proteins licensed from the Broad Institute,” said Rahul Dhanda, co-founder, president and CEO of Sherlock Biosciences. “With the addition of these exclusive Cas12 rights to Sherlock’s IP portfolio, as well as partnering with Tolo as our exclusive partner in China, we have secured our position as the global leader in CRISPR diagnostics.”"The advent of CRISPR technology is ushering in the next generation of molecular diagnostics,” said Jin Wang, co-founder and chief science officer of Tolo Biotech. “This agreement with Sherlock will enable both companies to develop diagnostic tools that can detect multiple pathogens or targets, improving disease screening, precision medicine and beyond. Tolo highly values this opportunity for close collaboration with Sherlock to promote the development of CRISPR diagnostics.”The SHERLOCK diagnostic platform can achieve single molecule detection of nucleic acid targets; its name stands for Specific High Sensitivity Enzymatic Reporter unLOCKing. SHERLOCK utilizes CRISPR activity for “smart amplicon detection” and can be adapted for use with existing diagnostic instruments, improving time to result due to its significant multiplexing capacity. When a specific sequence of DNA or RNA is present, a CRISPR enzyme is activated and, much like a pair of scissors, starts cutting nearby genetic material, releasing a fluorescent signal that indicates a positive result. In May 2020, Sherlock received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for its Sherlock™ CRISPR SARS-CoV-2 kit, the first FDA-authorized use of CRISPR technology.