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Cystic FibrosisKaf-PseudoNCT05675592

Trikafta/Kaftrio and Pseudomonas Aeruginosa

An observational study of Cystic Fibrosis, run by Ospedale San Raffaele at 2 sites in Italy.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The goal of this observational study o is to define whether, how and to what extent treatment with Trikafta/Kaftrio directly affects Pseudomonas aeruginosa in individuals with cystic fibrosis. Read more about this study

Who is it for?
Ages 12 years and older
Conditions the study is for
Cystic Fibrosis
How many people
20 participants
Where
2 sitesItaly
Study dates
22 Feb 2022to 16 May 2025
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 12 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: 20 patients with CF (from IRCCS Ca' Granda Foundation, Ospedale Maggiore Policlinico, Milan; IRCCS Pediatrico Bambino Gesù, Rome) will be enrolled. Currently, some patients already started treatment with Kaftrio and P. aeruginosa strains have been recovered for other studies. Of these patients, we will include only those for whom clonal strains at T0, T12m and T18m will be identified. If the number of retrospective patients is sufficient, no other patients will be recruited prospectively. Once enrolled, patients may drop out of the study if: 1. they are unable to expectorate at T12m and T18m; 2. the sputum is negative for P. aeruginosa at T12m or T18m; 3. none of the P. aeruginosa strains isolated at T12m and T18m is clonal to at least one strain isolated at T0. If the dropout is higher than expected, recruitment will continue until the necessary number of samples to be analyzed is obtained.

Who may be able to join

  • Definite diagnosis of CF and regular follow up, in accordance with the standard operating procedures in force at the Centres
  • Homozygous for the F508del mutation (F508del/F508del) in the CFTR gene or heterozygous for the F508del mutation and with a minimal function mutation in the other allele (F508del/minimum function mutation)
  • Chronically infected with P. aeruginosa (defined as having at least 50% or more sputum cultures positive for P. aeruginosa in the previous year)
  • Candidates starting treatment with Kaftrio or being treated with Kaftrio (retrospective phase)
  • Both sexes aged >12 years
  • Obtaining informed consent from patients and/or from patients' parents (according to the modalities foreseen by the protocol)

Who cannot join

  • Patients unable to understand the instructions and information provided and to be able to adequately accept the modalities of the study.
  • Patients unable to expectorate.
  • Patients with negative sputum for P. aeruginosa at T0, which in the case of prospective patients corresponds to the time of enrollment.

Trial locations and contacts

2 sites in 1 country.

Cristina Cigana, PhD contact

+390226434138

cigana.cristina@hsr.it

Alessandra Bragonzi, PhD contact

+390226434138

bragonzi.alessandra@hsr.it

Italy2 sites, 2 recruiting
  • UOC Pediatria Fibrosi Cistica, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

    Milan, 20132

    Daniela Girelli, Msc, +390255032574, daniela.girelli@policlinico.mi.it

    Arianna Biffi, Msc, arianna.biffi@policlinico.mi.it

    Recruiting
  • UOC Fibrosi Cistica, IRCCS Ospedale Pediatrico Bambino Gesù

    Rome, 00165

    Ersilia Vita Fiscarelli, MD, PhD, +390668593544, evita.fiscarelli@opbg.net

    Recruiting

Other trials in Italy

About this study

Official title: Linking Elexacaftor/Tezacaftor/Ivacaftor to Infections in Cystic Fibrosis Lung Disease

The goal of this observational study o is to define whether, how and to what extent treatment with Trikafta/Kaftrio directly affects Pseudomonas aeruginosa in individuals with cystic fibrosis. The main questions it aims to answer are:

  • whether Trikafta/Kaftrio affects the bacterial phenotypes and susceptibility to antibiotics;
  • whether Trikafta/Kaftrio impacts the bacterial virulence. Participants will be asked the permission to store and analyze P. aeruginosa isolates collected from respiratory samples for usual care plans before the initiation of treatment with Trikafta/Kaftrio and after 12 and 18 months of treatment. The results of bacterial analysis will be matched with clinical data at the specific time-points.

We expect to define effects of Trikafta/Kaftrio on P. aeruginosa and identify bacterial phenotypes as possible risk factors for its efficacy.

Read the detailed description

We will recruit 20 individuals affected by cystic fibrosis (≥12 years of age), chronically infected with P. aeruginosa (defined as having at least 50% or more sputum cultures positive for P. aeruginosa in the previous year), homozygous for the F508del mutation (F508del/F508del) or heterozygous for the F508del mutation and with a minimal function mutation in the other allele (F508del/minimal function), candidates for treatment with Trikafta/Kaftrio according to clinical practice. P. aeruginosa strains will be collected from the sputum before the start of therapy (T0) and after 12 (T12m) and 18 (T18m) months of treatment with Trikafta/Kaftrio. Currently, some patients have already started treatment with Trikafta/Kaftrio. The strains at T0 and for some of them also at T12m and T18m have already been recovered from these patients for other studies. Of these strains it is not yet known whether they are clonal at different times (T0, T12m and T18m). Of these patients, we will include in the expected 20 (20 total between prospective and retrospective) only patients for whom strains clonal between T0, T12m and T18m will be identified, asking for their authorization to use the strains and their data through informed consent. If the number of retrospective patients is sufficient to reach the expected number (20 total patients), no other patients will be recruited prospectively.

Patients who will be prescribed Trikafta/Kaftrio therapy according to clinical practice will be recruited at routine visits. The decision to prescribe treatment with Trikafta/Kaftrio, according to current clinical practice, is completely independent of the decision to include the patient in this study. The diagnostic and evaluation procedures and follow-up visits foreseen by the study will coincide with those programmed for each patient according to the standard operating procedures in force at the participating centres.

For retrospective patients, informed consent will be collected during the routine check-up and, once the eligibility criteria have been verified, the data relating to the visit performed before the start of therapy (T0) and, if already available, the data relating to the visit performed at 12 and 18 months from the beginning of the therapy (T12m and T18m), will be collected. P. aeruginosa recovered from the respiratory samples during the three visits will be analysed. In the event that data are not available, data and samples will be collected at the respective routine follow-ups (at 12 and/or 18 months).

For prospective patients, the enrollment visit will be performed during the routine visit performed before the start of therapy (T0) which will be followed by visits scheduled for clinical practice at 12 and 18 months from the start of therapy (T12m and T18m).

At T0, T12m and T18m the sputum samples, collected from the patient's airways, will be treated according to standard procedures for the evaluation of the bacterial species present. P. aeruginosa strains will be subjected to minimal inhibitory concentration tests to assay their susceptibility to a panel of standard antibiotics, and analyzed by Multi-locus Sequence Typing to detect their clonality.

The strains of each patient that will be clonal between T0, T12m and T18m, immediately stored at -80°C, will then be shipped to Ospedale San Raffaele , where they will be analyzed for the purposes of the project using methods validated in the literature. We will analyze i) the phenotypes (in particular motility by pilus, motility by flagellum, secretion of proteases and pyocyanin, and mucoidity) of P. aeruginosa strains using microbiological methods validated in the literature, ii) the expression profiles of the strains by RNA sequencing, iii) the presence of gene variants by whole genome sequencing of the strains, iv) and their virulence by measuring their impact on the expression of the cystic fibrosis transmembrane conductance regulator protein in cystic fibrosis bronchial epithelial cell lines.

The final aim will be to i) evaluate the differences in the phenotypes of the P. aeruginosa strains isolated at T0 and those isolated at T12m and T18m post treatment with Kaftrio; ii) to evaluate differences in the susceptibility to antibiotics of the P. aeruginosa strains isolated at T0 and those isolated at T12m and T18m; iii) evaluate differences in the expression profiles of the P. aeruginosa strains isolated at T0 and those isolated at T12m and T18m and correlate them to the difference in respiratory function measured as FEV1 (%); iv) evaluate the presence of gene variants between the strains isolated at T0 and those isolated at T12m and T18m and correlate them to the difference in respiratory function measured as FEV1 (%); v) to determine whether changes in bacterial phenotypes induced by Kaftrio treatment may be associated with lower anti-CFTR activity of P. aeruginosa.

Conditions
Cystic Fibrosis
Keywords
Trikafta, Pseudomonas aeruginosa, susceptibility to antibiotics, bacterial phenotype, bacterial transcriptome, bacterial genome, bacterial virulence
Medical subject headings
Cystic Fibrosis, Pseudomonas Infections

What is being measured

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

  1. bacterial phenotypes

    motility by pilus, motility by flagellum, secretion of proteases, secretion of pyocyanin of P. aeruginosa strains isolated at T0 and clonal ones isolated at T12m and T18m post treatment with Trikafta/Kaftrio

    Measured: 0-18 months

  2. respiratory function

    respiratory function, evaluated as FEV1 (%), measured at time at T0, T12m and T18m post Trikafta/Kaftrio treatment

    Measured: 0-18 months

Secondary outcomes (5)
  1. susceptibility to antibiotics

    susceptibility of P. aeruginosa strains isolated at T0 and those isolated at T12m and T18m to standard antibiotics evaluated by minimal inhibitory concentration assays

    Measured: 0-18 months

  2. mucoidy

    mucoidy of the P. aeruginosa strains isolated at T0 and those isolated at T12m and T18m determined by visual assessment of the growth in the plate

    Measured: 0-18 months

  3. expression profile

    expression profiles of the P. aeruginosa strains isolated at T0 and those isolated at T12m and T18m evaluated by RNA sequencing

    Measured: 0-18 months

  4. genetic variants

    presence of gene variants, identified by whole genome sequencing, between the strains isolated at T0 and those isolated at T12m and T18m

    Measured: 0-18 months

  5. impact on CFTR

    Membrane expression of CFTR protein, measured by western blot, in FC and non-FC immortalized bronchial epithelial cell lines stimulated with growth media of P. aeruginosa strains isolated at T0 and those isolated at T12m and T18m

    Measured: 0-18 months

Timeline

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

  1. First posted9 Jan 2023
  2. Study start22 Feb 2022
  3. Primary completion16 Nov 2023 (estimated)
  4. Study completion16 May 2025 (estimated)

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
Other
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05675592
Sponsor's protocol ID
173/INT/2021
Other IDs
FFC#16/2021
Acronym
Kaf-Pseudo
Status last verified
Jan 2023
First submitted
28 Dec 2022
Last updated
11 Jan 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: We are going to discuss this issue

Questions about this trial

What is this clinical trial studying?

An observational study of Cystic Fibrosis, run by Ospedale San Raffaele at 2 sites in Italy.

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 6 inclusion and 3 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: status not confirmed, as of the sponsor's last update on 11 Jan 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Italy. 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?

Results are not available in the source record.

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

Contact Cristina Cigana, PhD (+390226434138, cigana.cristina@hsr.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

bacterial phenotypes (time frame: 0-18 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 11 Jan 2023.

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