Agenovir Corp. won't use gene-editing to cut out defects or add in missing pieces in a patient's genome like most companies that are working with CRISPR/Cas9 constructs. Instead, it will use the technology to kill DNA that sits in latent viral reservoirs.
South San Francisco-based Agenovir believes that it has carved out a unique niche in the gene-editing space. The company's lead drug candidate, which could move into a clinical trial by...
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