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Randomization and administration of investigational drug Participants ( n = 39, Intention to Treat (ITT) population) with severe or moderate IPTB risk were randomized to receive either a high-dose NAC regimen or placebo per os , preceded by an initial intravenous ( iv )-infusion in the subgroup of severe IPTB (Fig

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If youre within 48 hours of your scheduled dose, take it as soon as you remember, then resume your regular schedule