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Trial · NCT07892443

Type 2 Inflammation in Adults With Cystic Fibrosis

NCT07892443, Not yet recruiting, University of Virginia

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Type 2 Inflammation in Adults With Cystic Fibrosis. Trials, record NCT07892443. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07892443

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Type 2 Inflammation in Adults With Cystic Fibrosis
NCT number
NCT07892443
Status
Not yet recruiting
Enrollment
100 participants, estimated
Lead sponsor
University of Virginia
Conditions
Cystic Fibrosis (CF), Type 2 Inflammatory Disorders
First posted
2026-10-23
Last updated
2026-10-23

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryBaseline Stable-State Absolute Peripheral Blood Eosinophil CountBaseline
Absolute peripheral blood eosinophil count measured during clinical stability at baseline. Eosinophil counts will be compared between participants who, after 36 months of prospective observation, are classified as having modulator-refractory CF (average of ≥2 qualifying pulmonary exacerbations per year) or modulator-responsive CF (average of \<2 qualifying pulmonary exacerbations per year).
SecondaryChange in Nasal Epithelial Gene Expression from Baseline to Pulmonary ExacerbationBaseline and qualifying pulmonary exacerbations occurring up to Month 36.
Within-participant changes in nasal epithelial gene expression from stable-state baseline to qualifying pulmonary exacerbations will be evaluated using RNA sequencing. Exploratory analyses will characterize changes in gene-expression patterns associated with type 2 inflammation and recurrent pulmonary exacerbations in adults with cystic fibrosis.
SecondaryChange in Exhaled Breath Condensate Inflammatory Mediator Concentrations from Baseline to Pulmonary ExacerbationBaseline and qualifying pulmonary exacerbations occurring up to Month 36.
Within-participant changes in inflammatory mediator concentrations in exhaled breath condensate will be evaluated between stable-state baseline and qualifying pulmonary exacerbations. These analyses will explore noninvasive biomarkers of airway inflammation and their association with changes in clinical state.
SecondaryChange in Peripheral Blood Immune Cell Phenotypes from Baseline to Pulmonary ExacerbationBaseline and qualifying pulmonary exacerbations occurring up to Month 36.
Within-participant changes in peripheral blood immune-cell populations from stable-state baseline to qualifying pulmonary exacerbations will be characterized using high-dimensional flow cytometry. Analyses will emphasize changes in the frequency of CRTH2-positive CD4-positive Th2 effector cells, with exploratory characterization of additional immune-cell populations associated with type 2 inflammation.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
39543951BACKGROUND

Source PubMed

Grants1

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
K23HL183757Importance of type 2 inflammation in cystic fibrosis patients with recurrent pulmonary exacerbationsSomerville, Lindsay A. L.UNIVERSITY OF VIRGINIANATIONAL HEART LUNG AND BLOOD INSTITUTE2026

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07892443

GET https://conductscience.org/api/trials/v1/NCT07892443/registered