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(Beijing, China) and ultraviolet spectrophotometry at a wavelength of 340 nm, in accordance with the manufacturers instructions

in the second single ascending dose Phase 1b trial (NCT02648269) composed of both a double-blind and open-label parts, we evaluate the safety of ImmTOR (primary endpoint) and its ability to prevent the formation of anti-drug antibodies against pegadricase and enhance its pharmacodynamic activity (secondary endpoint) in patients with hyperuricemia

A solution of 0.1% TFA gives a pH of approximately 1.82.0 in aqueous solutions [59]Snyder LR, Kirkland JJ, Glajch JL

AATS 105th Annual Meeting

doi: 10.1161/CIRCULATIONAHA.115.020406 8

2061-A INTEGRATION OF THE ENHANCED LIVER FIBROSIS (ELF) TEST FOR ADVANCED FIBROSIS AND CIRRHOSIS DETECTION IN A REAL-WORLD CLINICAL ENVIRONMENT Jessica C