A Study to Evaluate the Safety and Efficacy of Long Term Treatment With VX-661 in Combination With Ivacaftor in Subjects With Cystic Fibrosis Who Have an F508del-CFTR Mutation
Status: | Enrolling by invitation |
---|---|
Conditions: | Pulmonary |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 12 - Any |
Updated: | 11/24/2018 |
Start Date: | August 2015 |
End Date: | September 2019 |
A Phase 3, Open-label, Rollover Study to Evaluate the Safety and Efficacy of Long Term Treatment With VX-661 in Combination With Ivacaftor in Subjects Aged 12 Years and Older With Cystic Fibrosis, Homozygous or Heterozygous for the F508del-CFTR Mutation
This is a Phase 3, multicenter, open-label, 2-part rollover study in subjects with CF who are
homozygous or heterozygous for the F508del-CFTR mutation and who participated in Studies
NCT02070744, NCT02347657, NCT02516410, NCT02392234, NCT02412111, and NCT02508207. The study
is designed to evaluate the safety and efficacy of long term treatment of VX-661 in
combination with ivacaftor.
homozygous or heterozygous for the F508del-CFTR mutation and who participated in Studies
NCT02070744, NCT02347657, NCT02516410, NCT02392234, NCT02412111, and NCT02508207. The study
is designed to evaluate the safety and efficacy of long term treatment of VX-661 in
combination with ivacaftor.
Inclusion Criteria:
Part A:
- Subjects entering the Treatment Cohort must meet all of the following criteria:
- Elect to enroll in the Treatment Cohort
- Completed study drug Treatment Period in a parent study (NCT02070744, NCT02347657,
NCT02516410, NCT02392234, NCT02412111) or study drug treatment and the Safety Follow
up Visit for subjects from NCT02508207.
- Willing to remain on a stable CF regimen through the Safety Follow-up Visit.
- Subjects re-enrolling in the Part A Treatment Cohort must meet all of the following
criteria:
- Previously received at least 4 weeks of study drug before discontinuing in Part A
of Study NCT02565914 to participate in another qualified Vertex study.
- Completed the last required visit of another qualified Vertex study before or
during the Returning Visit in Part A Study NCT02565914.
- Subjects entering the Part A Observational Cohort must meet the following criteria:
- <18 years of age (age on the date of informed consent/assent in the parent study)
- Completed study drug Treatment Period in a parent study or study drug treatment
and the Safety Follow up Visit for subjects from NCT02508207, but do not elect to
enroll in the NCT02565914 Treatment Cohort; or
- Received at least 4 weeks of study drug treatment and completed visits up to the
last scheduled visit of the Treatment Period of a parent study (and the Safety
Follow up Visit for subjects from NCT02508207), but do not meet eligibility
criteria for enrollment into the Treatment Cohort
Part B:
Part B Subjects who meet all of the following inclusion criteria will be eligible for Part
B.
- Did not withdraw consent from the parent study or Part A of Study NCT02565914.
- Completed study drug treatment during the Treatment Period in Part A of NCT02565914,
Studies NCT02730208 or NCT03150719, or other eligible Vertex studies.
- Willing to remain on a stable CF medication (and supplement) regimen through the 96
week visit of Study NCT02565914.
Subjects re enrolling in Part B must meet all of the following criteria:
- Previously received at least 4 weeks of study drug before discontinuing Study
NCT02565914 to participate in another qualified Vertex study, which is defined as a
Vertex study of investigational CFTR modulators that allows participation of subjects
in Study NCT02565914.
- Completed the last required visit of another qualified Vertex study before or during
the Returning Visit in Part B.
- Willing to remain on a stable CF medication (and supplement) regimen through the 96
week visit in Part B.
Exclusion Criteria:
- History of any comorbidity that, in the opinion of the investigator, might confound
the results of the study or pose an additional risk to the subject.
- Pregnant and nursing females.
- Sexually active subjects of reproductive potential who are not willing to follow the
contraception requirements.
- History of drug intolerance in the parent study that would pose an additional risk to
the subject.
- Participation in an investigational drug trial (including studies investigating
VX-661/ivacaftor or lumacaftor/ivacaftor) other than the parent studies of NCT02565914
or other eligible Vertex studies investigating VX-661 in combination with ivacaftor,
or use of a commercially available CFTR modulator.
Other protocol defined Inclusion/Exclusion criteria may apply.
We found this trial at
70
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