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A minimum of an 8-week cycle and a maximum of 16 weeks is recommended with injections administered once per week

A phase 1/2, randomized, double-blinded, placebo-controlled, combined single and multiple ascending dose study evaluating the safety, tolerability, and biological activity of MRT5005 administered by nebulization to adult subjects with cystic fibrosis

Consequently, many research programs emphasize documentation, consistency, and quality-focused evaluation procedures throughout the research process

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