The U.S. Food and Drug Administration on Tuesday issued new draft guidance on reducing the use of lab monkeys in preclinical toxicity studies for certain monoclonal antibodies.
The agency said the shift would help cut development times and reduce research and development costs, which could translate into lower drug prices.
Under current FDA requirements for monoclonal antibodies, companies conduct studies in animals to test for any harmful effects of a drug.
US FDA moves to curtail primate testing in drug trials
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