Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Vertex Pharmaceuticals Incorporated
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Male or female participants with confirmed diagnosis of CF
Must have the F508del-CFTR mutation on at least 1 allele.
FEV1 greater than equal (\>=) 40% of predicted normal for age, gender, and height (Knudson standards)(Cohort 1, 2, and 3); FEV1 40-90% of predicted normal for age, gender, and height (Hankinson standards (Cohort 4)
Participant of child-bearing potential and who are sexually active must meet the contraception requirements
You may not be if
History of any illness or condition that, in the opinion of the investigator might confound the results of the study or pose an additional risk in administering study drug to the participant (e.g., cirrhosis with portal hypertension).
An acute illness including acute upper or lower respiratory infection, pulmonary exacerbation or changes in therapy (including antibiotics) for pulmonary disease within 14 days (Cohort 1, 2, and 3) or 28 days (Cohort 4) before receiving the first dose of study drug.
History of solid organ or hematological transplantation.
History of alcohol abuse or drug addiction in the past year, including cannabis, cocaine, and opiates.
Ongoing participation in another therapeutic clinical study, or prior participation in an investigational drug study without appropriate washout
Pregnant or nursing females; females of childbearing potential who are unwilling or unable to use an acceptable method of non-hormonal contraception
Participants enrolled in Cohort 1 or Cohort 2 will not be eligible for Cohort 3
Ongoing or prior participation in an investigational drug study within 30 days of the Screening Visit
Heterozygous participants who participated in Cohort 2 and meet the eligibility criteria for Cohort 4 may participate in Cohort 4
Evidence of lens opacity or cataract as determined by the ophthalmologic examination (Cohort 4 only)
Clareo Health | Study of VX-809 Alone and in Combination With VX-770 in Cystic Fibrosis (CF) Patients Homozygous or Heterozygous for the F508del-CFTR Mutation
