4-week-old infants can safely use Ivacaftor (Kalydeko) for cystic fibrosis, expanding treatment options.

A new study indicates that a cystic fibrosis drug, Ivacaftor (Kalydeko), is safe and effective for newborn babies aged four weeks and above. This marks a significant breakthrough in Cystic Fibrosis treatment, opening up earlier intervention possibilities for infants. Currently, the drug is approved for use in babies aged four months and older, but the new research suggests it can also be effective for infants as young as four weeks.

April 10, 2024
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