BEGIN Novel ImagiNG Biomarkers

Description

To determine the treatment effect of triple-combination therapy in 6-8 year olds after presumed FDA approval, using rapid structural and functional pulmonary and abdominal MRI (UTE and 129Xe).

Conditions

Cystic Fibrosis

Study Overview

Study Details

Study overview

To determine the treatment effect of triple-combination therapy in 6-8 year olds after presumed FDA approval, using rapid structural and functional pulmonary and abdominal MRI (UTE and 129Xe).

BEGIN Novel ImagiNG Biomarkers

BEGIN Novel ImagiNG Biomarkers

Condition
Cystic Fibrosis
Intervention / Treatment

-

Contacts and Locations

Kansas City

University of Kansas Medical Center, Kansas City, Kansas, United States, 66160

Cincinnati

Carrie Stevens, Cincinnati, Ohio, United States, 45229

Charlottesville

University of Virginia, Charlottesville, Virginia, United States, 22903

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Written informed consent (and assent where appropriate) obtained from the subject or subject's legal representative.
  • 2. Willingness to adhere to the study-visit schedule and other protocol requirements.
  • 3. Ages 6-8 years old at baseline MRI visit (may be enrolled up to 60 days before 6th birthday).
  • 4. Documentation of CF diagnosis as evidenced by one or more clinical features consistent with the CF phenotype and one or more of the following criteria:
  • 1. Sweat chloride equal to or greater than 60 mEq/liter by quantitative pilocarpine iontophoresis test
  • 2. Two well-characterized mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene
  • 5. Physician intent to prescribe triple-combination therapy
  • 6. Clinically-stable with no respiratory tract infection at the time of enrollment.
  • 7. No change in chronic maintenance therapies in the 28 days prior to enrollment.
  • 8. Ability to cooperate with MRI procedures
  • 1. Individuals currently on ivacaftor therapy (including Kalydeco, Orkambi, and Symdeko) and with at least one gating mutation. Gating mutations include G551D, G178R, S549N, S549R, G551S, G970R, G1244E, S1251N, S1255P, or G1349D.
  • 2. Acute respiratory symptoms (e.g. wheezing) at the time of the MRI.
  • 3. Acute respiratory infection, defined as increased cough, wheezing or respiratory rate in the 28 days prior to enrollment.
  • 4. Chronic lung disease not related to CF
  • 5. Chronic liver disease not related to CF
  • 6. Acute pancreatitis, defined by clinical criteria (45).
  • 7. Chronic pancreatic disease not related to CF.
  • 8. Physical findings that would compromise the safety of the subject or the quality of the study data as determined at the discretion of the site investigator.
  • 9. Any other condition that, in the opinion of the Site Investigator/designee, would preclude informed consent or assent, make study participation unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.

Ages Eligible for Study

6 Years to 8 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Children's Hospital Medical Center, Cincinnati,

Jason Woods, PhD, PRINCIPAL_INVESTIGATOR, Children's Hospital Medical Center, Cincinnati

Study Record Dates

2028-11-01