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Inflammatory Changes in Epithelial Lining Fluid Sampled Non-invasively by Nasal Lavage in CF Patients With G551D Receiving KalydecoKPNSINCT02311140

Effects of Kalydeco on Upper Airway and Paranasal Sinus Inflammation Measured by Nasal Lavage and on Symptoms

An observational study of Inflammatory Changes in Epithelial Lining Fluid Sampled Non-invasively by Nasal Lavage in CF Patients With G551D Receiving Kalydeco, run by University of Jena at 1 site in Germany.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The aim of the proposed trial in assessment of effects of Kalydeco™ treatment on sinonasal involvement in CF patients with at least one mutation of G551D receiving a new therapy with the CFTR potentiator. Read more about this study

Who is it for?
Ages 6 years and older
What is being tested?
nasal lavage (routine diagnostic procedure in our centre), assessment of symptoms
How many people
10 participants
Where
1 siteGermany
Study dates
Jul 2012to Dec 2018
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: CF patients with G551D mutation receiving Kalydeco

Who may be able to join

  • G551D and Kalydeco therapy

Who cannot join

  • no G551D

Trial locations and contacts

1 site in 1 country.

Germany1 site
  • Jena University Hospital, CF Center

    Jena, 07743

Other trials in Germany

About this study

The aim of the proposed trial in assessment of effects of Kalydeco™ treatment on sinonasal involvement in CF patients with at least one mutation of G551D receiving a new therapy with the CFTR potentiator. The focus will be given on changes in epithelial lining fluid inflammatory markers from CF upper airways sampled by nasal lavage.

The program is subdivided into a part A assessing inflammatory markers in NL and sinonasal symptoms longitudinally from pre-treatment to months with the new therapy.

Part B will only be performed in a smaller subgroup and assess inflammatory markers in NL every second day in the first month of treatment and then every week until the end of month 3 with Kalydeco™ therapy.

Read the detailed description

Enrollment of Patients In this longitudinal trial, 10 CF patients with a G551D mutation, newly receiving ivacaftor 150 mg bid, as approved (1), were included in the Jena (Germany) and Innsbruck (Austria) University CF centers. Inclusion criteria were: CF patients' age ≥ 6 years with a diagnosis confirmed by two positive sweat tests and/or detection of two disease-causing CFTR mutations; one of them being G551D. Patients were required to strictly follow the procedures defined in the SOPs and they and/or their parents gave informed written consent prior to enrolment. Exclusion criteria were: inability to perform NL in a standardized manner as described below, contraindication for ivacaftor, pregnancy or breast-feeding, and participation in another clinical study within 30 days prior to study drug administration. Nasal Lavage Patients were thoroughly trained to perform NL in standardized home-based conditions (Figures 1A-C) by using the instructionvideo from our publication in Journal of Immunological Methods 2014 (14) and an illustrated SOP sheet. The pooled native NLF was transferred into disposed reaction tubes containing 15 μL of protease inhibitor (Figures 1D, E) and, within 30 minutes after sampling, stored in a freezer below -18°C until transfer on ice to the centers. Here, the vials were directly stored at - 80°C until performance of laboratory analyses. Prior to the initiation of ivacaftor therapy, NL was collected at least once a week (mean: 5.5 ± 3.9 samplings/patient) during a mean time of 30.3 ± 19.7 days. During the first month of therapy (days 0-30), NL was collected every second day and once/week from month two onward (mean: 25.9 ± 4.1 samplings/patient). Follow-up range after initiation of ivacaftor: 2.3-16.1 months, (median: 5.7 months). Assessment of Inflammatory Mediators Concentrations of IL-1b, IL-6, and IL-8 were measured in undiluted NL fluid using Milliplex® MAP Kits (Human High Sensitivity HS TCMAG-28K, Merck Millipore; Darmstadt, Germany) and a Bio-Plex® 200 system (Bio-Rad; Hercules, California, USA) according to the manufacturer's instructions. Measurements of Neutrophil Elastase (NE) were performed using Human PMN Elastase ELISA (DEH3311, Demeditec Diagnostics GmbH; Kiel, Germany) and read by a FLUOstar Galaxy spectrometer (BMG LABTECH GmbH; Offenburg, Germany). As specified by the manufacturer, lower detection limits were 0.12 pg/mL (IL-1b), 0.13 pg/mL (IL-6), 0.12 pg/mL (IL-8), and 0.2 ng/mL (NE). Statistical Analyses Descriptive statistics were used to describe clinical characteristics of the study population. Linear mixed-effects models were performed to analyze overall trends of inflammatory markers. To smooth effects caused by outliers in inflammatory marker values, individual changes regarding cumulative periods for each patient were determined by calculating medians for the time periods before and after treatment initiation (i.e. regarding periods of 4, 8 and 12 weeks during treatment as shown in Figure 2). The resulting individual patients' medians were used to calculate medians and interquartile ranges (IQR) of the entire cohort at the end of the above-mentioned time periods. Wilcoxon signedrank test (two-tailed) was applied to determine changes in the aforementioned inflammatory mediators, sweat test, FEV1 and their statistical significance (using p<0.05) during the new therapy. All statistical analyses were performed with IBM SPSS 19 (SPSS Inc., Chicago, IL, USA); figures were created with GraphPad Prism (GraphPad Software Inc., La Jolla, CA, USA).

Being tested
nasal lavage (routine diagnostic procedure in our centre), assessment of symptoms
Keywords
cystic fibrosis, nasal lavage, inflammation, Interleukin (IL)-6, IL-8, pulmonary function
Medical subject headings
Cystic Fibrosis, Inflammation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • nasal lavage (routine diagnostic procedure in our centre), assessment of symptomsOther

Study groups in NCT02311140
Study groupRoleWhat they receive
Cystic Fibrosis patients with G551D mutationCohort Description Ten participants (6 Jena/4 Innsbruck) were included, of whom 6 were female and 4 were male. At the start of the study, patients were aged 7-45 years (mean age: 16.55 ± 13.42 years). Results of sweat tests and lung function FEV1 were available only from 8 patients. Lung function at baseline, as obtained from those patients, ranged from 0.96 to 4.07 L (mean FEV1: 99.7 ± 20.3% predicted, median: 103.6% predicted, IQR=20.4% predicted).
Receives: Other: nasal lavage (routine diagnostic procedure in our centre), assessment of symptoms

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Changes in concentration of inflammatory markers

    Concentrations of IL-1b, IL-6, and IL-8 were measured in undiluted NL fluid using Milliplex® MAP Kits (Human High Sensitivity HS TCMAG-28K, Merck Millipore; Darmstadt, Germany) and a Bio-Plex® 200 system (Bio-Rad; Hercules, California, USA) according to the manufacturer's instructions. Measurements of Neutrophil Elastase (NE) were performed using Human PMN Elastase ELISA (DEH3311, Demeditec Diagnostics GmbH; Kiel, Germany) and read by a FLUOstar Galaxy spectrometer (BMG LABTECH GmbH; Offenburg, Germany). As specified by the manufacturer, lower detection limits were 0.12 pg/mL (IL-1b), 0.13 pg/mL (IL-6), 0.12 pg/mL (IL-8), and 0.2 ng/mL (NE).

    Measured: 3 yrs

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Dec 2014 (estimated)
  2. Study startJul 2012
  3. Primary completionJun 2017
  4. Study completionDec 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
10 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02311140
Sponsor's protocol ID
UKJ-IVA-Nasal
Acronym
KPNSI
Status last verified
Jul 2021
First submitted
4 Dec 2014
Last updated
15 Jul 2021
Results posted
No
Data monitoring committee
No

Publications

  • Mainz JG, Arnold C, Wittstock K, Hipler UC, Lehmann T, Zagoya C, Duckstein F, Ellemunter H, Hentschel J. Ivacaftor Reduces Inflammatory Mediators in Upper Airway Lining Fluid From Cystic Fibrosis Patients With a G551D Mutation: Serial Non-Invasive Home-Based Collection of Upper Airway Lining Fluid. Front Immunol. 2021 May 5;12:642180. doi: 10.3389/fimmu.2021.642180. eCollection 2021.

    PubMed 34025651

Questions about this trial

What is this clinical trial studying?

An observational study of Inflammatory Changes in Epithelial Lining Fluid Sampled Non-invasively by Nasal Lavage in CF Patients With G551D Receiving Kalydeco, run by University of Jena at 1 site in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 15 Jul 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Changes in concentration of inflammatory markers (time frame: 3 yrs). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02311140, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Jul 2021.

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