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It used the FDA's new Commissioner's National Priority Voucher (CNPV) pathway a faster review track and became the first new molecular entity approved under that program

(Given the potential long-term consequences of NMOSD relapses, the company could not ethically include a direct placebo arm in its Phase III trial.) Ultomiris was well-tolerated overall, and most treatment-emergent events were mild or moderate in severity, according to AstraZeneca

It is found and made in every cell of the body, but occurs in higher concentrations in the heart, muscle tissue and liver

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