Cystic Fibrosis Clinical Trials in Boston, Massachusetts

11 studies are recruiting for cystic fibrosis in Boston, Massachusetts 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 now recruiting

  1. Streamlined Treatment of Pulmonary Exacerbations in Pediatrics

    The STOP PEDS RCT is a multicenter, parallel, open label randomized controlled trial evaluating the long-term (one year) and short-term safety and efficacy of two antibiotic treatment strategies for the management of outpatient pulmonary exacerbations (PEx) in the pediatric CF population.

    Stage
    Not phased
    Ages
    3 to 18
    Site
    Boston Children's Hospital & Harvard University, Boston, Massachusetts
    Locations
    33 in total
    Run by
    University of Washington, the Collaborative Health Studies Coordinating Center
  2. Study to Evaluate Biological & Clinical Effects of Significantly Corrected CFTR Function in Infants & Young Children

    This is a two-part, multi-center, prospective longitudinal, exploratory study of highly effective cystic fibrosis transmembrane conductance regulator (CFTR) modulators and their impact on children with cystic fibrosis (CF).

    Stage
    Not phased
    Ages
    Up to 10
    Site
    Boston Children's Hospital, Boston, Massachusetts
    Locations
    35 in total
    Run by
    Sonya Heltshe
  3. Standardizing Treatments for Pulmonary Exacerbations - Aminoglycoside Study

    The purpose of this study is to look at pulmonary exacerbations in people with cystic fibrosis (CF) that need to be treated with antibiotics given through a tube inserted into a vein (intravenous or IV). A pulmonary exacerbation is a worsening of respiratory symptoms in people with CF that needs me…

    Stage
    Phase 4
    Ages
    6 and older
    Site
    Boston Children's Hospital, Brigham & Women's Hospital, Boston, Massachusetts
    Locations
    60 in total
    Run by
    Chris Goss
  4. Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of SPL84 in Patients With Cystic Fibrosis

    The goal of this clinical trial is to learn if drug SPL84 is safe for adult patients with cystic fibrosis (CF). It will also learn if the drug works to treat works to treat CF with a specific mutation (3849 +10kb C-->T). The purpose of this research study is to test the safety and effectiveness of …

    Stage
    Phase 2
    Ages
    18 and older
    Site
    Boston Children'S Hospital, Boston, Massachusetts
    Locations
    3 in total
    Run by
    SpliSense Ltd.
  5. Safety, Tolerability and Efficacy Study of ARCT-032 in People With Cystic Fibrosis

    ARCT-032-02 is a Phase 2, open-label, multicenter, multiple-ascending dose study of ARCT-032 in adults with CF who are not eligible for CFTR modulator therapy or are not taking CFTR modulators due to drug intolerance, poor response, or lack of access to modulators.

    Stage
    Phase 2
    Ages
    18 and older
    Site
    Boston Children's Hospital, Boston, Massachusetts
    Locations
    13 in total
    Run by
    Arcturus Therapeutics, Inc.
  6. 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
    Massachusetts General Hospital, Boston, Massachusetts
    Locations
    18 in total
    Run by
    University of Pittsburgh
  7. 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
    Boston Children's Hospital, Boston, Massachusetts
    Locations
    18 in total
    Run by
    Boston Children's Hospital
  8. 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
  9. 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
    Massachusetts General Hospital, Boston, Massachusetts
    Locations
    68 in total
    Run by
    Nicole Hamblett
  10. 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
  11. 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
    Boston Children's Hospital, Brigham & Women's Hospital, Boston, Massachusetts
    Locations
    4 in total
    Run by
    Spirovant Sciences, Inc.

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.