Three years ago, Arbor Biotechnologies CEO Devyn Smith appeared at the J.P. Morgan Healthcare Conference and laid out a grand vision: With $215 million in new capital, the biotech would push forward CRISPR-based drugs for a series of liver and brain diseases, beginning by filing for a first trial in under two years.
It was, suffice to say, bold. Arbor had yet to even conduct a mouse experiment.
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“I mean, we set very aggressive targets,” Smith said in a recent interview. “You don’t set aggressive targets, you don’t get aggressive wins.”
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