Cystic Fibrosis Clinical Trials
45 studies are recruiting for cystic fibrosis in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies, page 2
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Dose Escalation Study Evaluating the Safety and Pharmacokinetics of VX-272 in Healthy Participants
The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics of single and multiple ascending doses of VX-272.
- Stage
- Phase 1
- Ages
- 18 to 55
- Site
- Celerion - Tempe, Tempe, Arizona
- Run by
- Vertex Pharmaceuticals Incorporated
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Exercise in Child Health
This study is a cooperative investigation funded by the NIH. The project is a collaboration among three major NIH Clinical Translational Science Awardees: 1) UCI (lead site with its affiliate CHOC), 2) Northwestern University (with its affiliate Lurie Children's Hospital), and 3) USC (with its affi…
- Stage
- Not phased
- Ages
- 10 to 17
- Site
- University of California, Irvine, Irvine, California
- Run by
- University of California, Irvine
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Personalized Theratyping Trial
The purpose of this study is to explore the use of off-label CFTR modulators that may affect CFTR function in patients with CFTR mutations that are not currently approved for these drugs.
- Stage
- EARLY_Phase 1
- Ages
- 6 and older
- Site
- University of Alabama at Birmingham, Birmingham, Alabama
- Run by
- George Solomon
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Beta-cell Response to Incretin Hormones in Cystic Fibrosis
In recent years, diabetes has emerged as one of the most significant co-diseases that many Cystic Fibrosis (CF) patients develop. Type 1 (T1D) and Type 2 (T2D) diabetes results when either the body does not make enough insulin or the body does not respond correctly to this insulin, respectively. In…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, Pennsylvania
- Run by
- University of Pennsylvania
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Regional Monitoring of CF Lung Disease
The main reason for this research study is to learn more about some new tests that are being developing for patients with Cystic Fibrosis (CF) to measure changes in the lungs. In this study, the focus will be to learn how stopping Airway Clearance (ACT) and re-starting ACT can affect these tests. T…
- Stage
- EARLY_Phase 1
- Ages
- 12 to 21
- Site
- Cincinnati Children's Hospital, Cincinnati, Ohio
- Run by
- Children's Hospital Medical Center, Cincinnati
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Skin-interfaced Colorimetric Bifluidic Sweat Sensor Device for the Diagnosis of Cystic Fibrosis (CF)
Cystic fibrosis (CF) is a multisystem autosomal recessive inherited disease affecting approximately 75,000 individuals in USA. The sweat chloride (Cl) test remains the gold standard for diagnosis of CF but still has a number of limitations. The objectives of this study are: 1)To evaluate a skin-int…
- Stage
- Not phased
- Ages
- 18 to 80
- Site
- Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania
- Run by
- Milton S. Hershey Medical Center
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Testing Drug Efficacy in Cystic Fibrosis Through N-of-1 Trials
The purpose of this study is to validate and utilize a personalized medicine approach to identify potential treatments with current FDA approved CFTR modifiers for non-approved CF gene mutations. The study will perform ex vivo testing of CFTR function and current marketed CFTR modulating drugs on e…
- Stage
- Not phased
- Ages
- 6 and older
- Site
- CCHMC, Cincinnati, Ohio
- Run by
- Children's Hospital Medical Center, Cincinnati
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Impact of Highly Effective Modulator Therapy on the Cystic Fibrosis Microbiome
The goal of this observational study is to learn about the effects of a specific cystic fibrosis therapy (Cystic Fibrosis Transmembrane Conductance Regulator Modulator Therapy) on chronic sinonasal disease. The main questions it aims to answer are: 1. How does this therapy impact bacterial communit…
- Stage
- Not phased
- Ages
- 18 to 99
- Site
- Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire
- Run by
- Dartmouth-Hitchcock Medical Center
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Estrogen Supplementation and Bone Health in Women With CF
The goal of this study is to learn about the role of estrogen and other hormones in bone development in adolescent and young adult women with cystic fibrosis (CF). The study has two main components, an observational study and a feasibility sub-study. The main questions it aims to answer are: * How …
- Stage
- Phase 4
- Ages
- 0 to 100
- Site
- Johns Hopkins, Baltimore, Maryland
- Run by
- Johns Hopkins University
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Health Outcomes of Parents With Cystic Fibrosis-Aim 2
The goal of this observational prospective study is to determine the health impact of parenthood on United States (US) people with CF in the era of CF transmembrane regulator protein (CFTR) modulators. The investigators will collect physical and mental health data to comprehensively evaluate the im…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Alabama-Birmingham, Birmingham, Alabama
- Locations
- 18 in total
- Run by
- University of Pittsburgh
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Restarting Triple Therapy With Robust Monitoring for Adverse Events (RETRIAL)
RETRIAL is a multi-site observational study of people with Cystic Fibrosis (PWCF) ages 6 and up starting the new triple-therapy modulator (vanzacaftor/tezacaftor/deutivacaftor (VTD)), after having experienced neuropsychiatric events and/or liver injury while taking elexacaftor/tezacaftor/ivacaftor …
- Stage
- Not phased
- Ages
- 6 and older
- Site
- University of Alabama at Birmingham, Birmingham, Alabama
- Locations
- 18 in total
- Run by
- Boston Children's Hospital
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Skeletal Health and Bone Marrow Composition in Adolescents With Cystic Fibrosis
The investigators will be evaluating bone marrow composition via magnetic resonance imaging in adolescents diagnosed with cystic fibrosis (CF) compared to healthy, matched controls. The investigators will also be assessing their bone mineral density via other imaging modalities, including dual-ener…
- Stage
- Not phased
- Ages
- 13 to 20
- Site
- Boston Children's Hospital, Boston, Massachusetts
- Run by
- Massachusetts General Hospital
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Acoustic Waveform Respiratory Evaluation
The study will evaluate the feasibility of using smartphone speakers and microphones to evaluate the caliber of the airways, detect airway obstruction, aid in airway disease diagnosis, and identify disease exacerbations.
- Stage
- Not phased
- Ages
- 8 to 70
- Site
- Indiana University, Indianapolis, Indiana
- Locations
- 2 in total
- Run by
- Indiana University
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A Research Study to Advance the CF Therapeutics Pipeline for People Without Modulators
The REACH study is for people with CF who do not take cystic fibrosis transmembrane conductance regulator (CFTR) modulators. The goal of the REACH study is to collect research data, including health data and specimens, from people with CF who do not take CFTR modulators. This data may be used to in…
- Stage
- Not phased
- Ages
- 12 and older
- Site
- The Children's Hospital Alabama, University of Alabama at Birmingham, Birmingham, Alabama
- Locations
- 68 in total
- Run by
- Nicole Hamblett
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The Effects of a Low Glycemic Load Diet on Dysglycemia and Body Composition in Adults With Cystic Fibrosis-Related Diabetes
This study will evalute the effect of a low glycemic load (LGL diet on dysglycemia, insulin requirements, DXA-derived body composition, gastrointestinal symptoms and quality of life measures in adults with cystic fibrosis-related diabetes (CFRD). We will use continuous glucose monitors (CGM) to ass…
- Stage
- Not phased
- Ages
- 18 to 70
- Site
- Boston Children's Hospital, Boston, Massachusetts
- Locations
- 2 in total
- Run by
- Rhode Island Hospital
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Targeting Inflammation With Losartan to Improve Response to Modulator Therapy in Cystic Fibrosis.
The goal of this clinical trial is to test use of losartan in those with cystic fibrosis (CF) on modulator therapy. The main question it aims to answer is if treatment with losartan improves response of the CF transmembrane conductance regulator (CFTR) channel to modulator therapy. Participants wil…
- Stage
- Phase 2
- Ages
- 12 and older
- Site
- University of Kansas Medical Center, Kansas City, Kansas
- Run by
- University of Kansas Medical Center
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Regional Phenotyping of CF and Non-CF Bronchiectasis
The Investigators propose to study pediatric subjects who are diagnosed with cystic fibrosis (CF) and patients with non-CF bronchiectasis, with the goal of developing markers of CF lung disease severity, progression, and therapy response. The Investigator's central hypothesis is that image-based ma…
- Stage
- Not phased
- Ages
- 5 to 100
- Site
- Penny New, Cincinnati, Ohio
- Run by
- Children's Hospital Medical Center, Cincinnati
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Lung Transplant READY CF 2: CARING CF Ancillary RCT
Lung transplant is an option for treating end-stage lung disease in cystic fibrosis (CF). In the United States, more people with CF and low lung function die each year than undergo lung transplant. More than half of people with CF who die without a lung transplant were never referred for considerat…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Washington Medical Center - Montlake, Seattle, Washington
- Run by
- University of Washington
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A Phase 1/2 Trial of SP-101 for the Treatment of Cystic Fibrosis (CF)
This is a Phase 1/2 multicenter, open-label, single dose trial of SP-101 investigational gene therapy in adults with CF who are ineligible for or intolerant to CFTR modulator therapy.
- Stage
- Phase 1
- Ages
- 18 to 65
- Site
- University of Kansas Medical Center, Kansas City, Kansas
- Locations
- 4 in total
- Run by
- Spirovant Sciences, Inc.
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BEGIN Novel ImagiNG Biomarkers
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).
- Stage
- Phase 4
- Ages
- 6 to 8
- Site
- University of Virginia, Charlottesville, Virginia
- Locations
- 3 in total
- Run by
- Children's Hospital Medical Center, Cincinnati
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.