BEGIN Novel ImagiNG Biomarkers

Cystic Fibrosis Clinical Trial

— BEGINNING  

Official title:

BEGIN Novel ImagiNG Biomarkers

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05517655
• Other study ID #: 2021-0325
• Status: Recruiting
• Phase: Phase 4
• Start date: May 1, 2022
• Est. completion date: November 1, 2028

Study information

• Verified date: October 2023
• Source: Children's Hospital Medical Center, Cincinnati
• Contact: Carrie Stevens, BS
• Phone: (513) 636-9973
• Email: carrie.stevens[@]cchmc.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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).

Description:

The overall hypothesis is that multi-organ MRI will provide more sensitive, robust outcome measures in young CF patients than traditional measures employed in the BEGIN study and that these novel measures will be more sensitive to treatment effects, tested here by comparison before and after triple-combination modulator therapy. By understanding the nature of early lung obstruction and characteristic changes in the liver and pancreas over time, we continue to lay the groundwork for more personalized medicine in the future.

Assessing treatment response and clinical benefit in children with CF who are clinically normal per standard outcomes (e.g., spirometry, pancreatic function) will become paramount as triplecombination therapy is extended to younger patients with milder CF clinical presentation than their historic peers. Here the sensitivity and profile free of ionizing-radiation exposure of MRI can be leveraged to follow an individual with CF over time to quantify changes with therapy-with additional spatial resolution unavailable from standard clinical testing.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 44
• Est. completion date: November 1, 2028
• Est. primary completion date: November 1, 2028
• Accepts healthy volunteers: No
• Gender: All
• Age group: 6 Years to 8 Years

Eligibility

Inclusion 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

Exclusion Criteria:

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.

Related Conditions & MeSH terms

• Cystic Fibrosis

Intervention

Drug:
• 129Xe
Rapid spatial mapping of lung, liver, and pancreatic structure and function is now possible with a combination of hyperpolarized 129Xe and traditional proton MRI, all absent sedation and ionizing radiation.

Locations

Country	Name	City	State
United States	University of Virginia	Charlottesville	Virginia
United States	Carrie Stevens	Cincinnati	Ohio
United States	University of Kansas Medical Center	Kansas City	Kansas

Sponsors (4)

Lead Sponsor	Collaborator
Children's Hospital Medical Center, Cincinnati	University of Iowa, University of Kansas, University of Virginia

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Ventilation Defect Percentage change from baseline	For pulmonary MRI, the primary outcome measure is the change in 129Xe ventilation defect percentage (VDP) from pre-therapy baseline to the one-year follow-up visit.	1 year
Primary	Pancreas volume	For pancreatic MRI, the primary outcome measure is change in pancreas volume normalized to BSA between pre-therapy baseline and one-year follow-up visit.	1 year
Secondary	Abdominal T1 values	Changes in MRI T1 average in the liver and pancreas, from baseline to follow up at 1 year	1 year
Secondary	Lung reader score	Changes in reader score for visible structural defects from proton MRI, from baseline to follow up at 1 year	1 year