AIR-CF1: Adverse Reactions

CAYSTON's safety profile was clinically evaluated in multiple studies

The safety profile of CAYSTON was evaluated in 344 patients from 2 placebo-controlled trials (AIR-CF1 and AIR-CF2) and 1 open-label follow-on trial (AIR-CF3).

In the 2 controlled trials, 146 patients with CF received 75 mg CAYSTON 3 times a day for 28 days.

Adverse reactions reported in ≥5% of patients treated with CAYSTON in the placebo-controlled trials

CAYSTON AIR-CF1: adverse reactions chart

Low incidence of altered taste: In AIR-CF1, dysgeusia (altered taste) was reported by 1 patient treated with 75 mg CAYSTON and 1 placebo-treated patient.4

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