U.S. FDA declines emergency use approval for Humanigen's COVID-19 drug

Sept 9 (Reuters) - The U.S. Food and Drug Administration declined Humanigen Inc's request for emergency use authorization of its lenzilumab drug to treat newly hospitalized COVID-19 patients, the company said on Thursday.

"In its letter, FDA stated that it was unable to conclude that the known and potential benefits of lenzilumab outweigh the known and potential risks of its use as a treatment for COVID-19," the company said in a statement. (Reporting by Aakriti Bhalla in Bengaluru; Editing by Shounak Dasgupta)