
In this Phase, IIb dose-finding trial, the CFTR potentiator icenticaftor (QBW251) was compared to a placebo in patients with COPD and chronic bronchitis. While the primary endpoint, FEV1 improvement over 12 weeks, wasn't met, cautious interpretation reveals positive results. Icenticaftor enhanced through FEV1, lessened cough, sputum, rescue medication use, and lowered fibrinogen levels at 24 weeks.
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