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For subjects who lack documentation of either a positive sweat chloride test or an abnormal NPD, and who have only one well-characterized genetic mutation of the CFTR gene, the diagnosis of CF is determined by the Investigator.\n* FEV1 ≥ 25% predicted and ≤ 90% predicted.\n* ≥ 2 lower respiratory tract cultures positive for PA with results documented in the subject's medical history.\n* Subject must be able to provide written informed consent\u002Fassent prior to any study related procedure; parent\u002Fguardian must be able to give written informed consent as necessary prior to any study related procedure.\n\nKey Exclusion Criteria:\n\nSubjects who meet the following exclusion criterion are not to be enrolled in this study.\n\n• Any serious active medical or psychiatric illness that, in the opinion of the Investigator, would interfere with subject assessment.\n\nNote: Other protocol defined Inclusion\u002FExclusion criteria may apply.","ALL","6 Years",{"count":300,"type":301},510,"ACTUAL","OBSERVATIONAL","This is a prospective, longitudinal, 5-year study that will enroll participants from the existing Cystic Fibrosis Foundation (CFF) patient registry. 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