Liquidia Technologies Reports Positive Interim LIQ861 Safety Data on 109 Patients from Pivotal INSPIRE Trial - Associated Press

Liquidia Technologies Reports Positive Interim LIQ861 Safety Data on 109 Patients from Pivotal INSPIRE Trial  Associated Press

LIQ861was well-tolerated in PAH patients at two-weeks of treatment, the safety endpoint requested by U.S. FDA -- NDA submission targeted for late 2019 ...



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