Cystic FibrosisKaf-PseudoNCT05675592
Trikafta/Kaftrio and Pseudomonas Aeruginosa
An observational study of Cystic Fibrosis, run by Ospedale San Raffaele at 2 sites in Italy.
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.
Italy2 sites, 2 recruiting
- 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
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.
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
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)
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
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
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
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
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.
- First posted9 Jan 2023
- Study start22 Feb 2022
- Primary completion16 Nov 2023 (estimated)
- Study completion16 May 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cystic FibrosisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Ospedale San Raffaele
- Sponsor type
- University, hospital or other
- Collaborators
- Ospedale Pediatrico Bambin Gesù, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
- Responsible party
- Principal investigator, Cristina Cigana, Ospedale San Raffaele
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
Study at a glance
From the registry record, last updated by the sponsor on 11 Jan 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Linking Elexacaftor/Tezacaftor/Ivacaftor to Infections in Cystic Fibrosis Lung Disease
- ClinicalTrials.gov ID
- NCT05675592
- Acronym / sponsor ID
- Kaf-Pseudo / 173/INT/2021
- Conditions
- Cystic Fibrosis
- Keywords
- Trikafta, Pseudomonas aeruginosa, susceptibility to antibiotics, bacterial phenotype, bacterial transcriptome, bacterial genome, bacterial virulence
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 20 participants (estimated)
- Lead sponsor
- Ospedale San RaffaeleUniversity, hospital or other
- Collaborators
- Ospedale Pediatrico Bambin Gesù, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
- Study start
- 22 Feb 2022 (actual)
- Primary completion
- 16 Nov 2023 (estimated)
- Study completion
- 16 May 2025 (estimated)
- First posted
- 9 Jan 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Other
Who may qualify
- Ages
- 12 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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.
Key inclusion criteria (6 listed)
- 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
Key exclusion criteria (3 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
bacterial phenotypes
Time frame: 0-18 months
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
respiratory function
Time frame: 0-18 months
respiratory function, evaluated as FEV1 (%), measured at time at T0, T12m and T18m post Trikafta/Kaftrio treatment
5 secondary outcomes
susceptibility to antibiotics
Time frame: 0-18 months
mucoidy
Time frame: 0-18 months
expression profile
Time frame: 0-18 months
genetic variants
Time frame: 0-18 months
impact on CFTR
Time frame: 0-18 months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Jan 2023.
- project behind this studyLink provided by the sponsor.
- Individual participant dataSharing planned: Undecided. We are going to discuss this issue
Related trials for Cystic Fibrosis
RecruitingObservational study
Role of Genetic Factors in the Development of Lung Disease
Cystic Fibrosis, Pulmonary Fibrosis
Active, not recruiting
Personalized Mobile Health Platform to Promote Physical Activity in Adolescents and Young Adults With Cystic Fibrosis
Cystic Fibrosis (CF)
RecruitingPhase 2
Early Study on Tamoxifen Safety/Tolerability in Cystic Fibrosis Patients Unable to Use CFTR Modulators.
Cystic Fibrosis - Complete
RecruitingObservational study
Natural History of Bronchiectasis
Bronchiectasis, Cystic Fibrosis
RecruitingPhase 1
Investigation of Pharmacokinetics, Safety of HSK31858 in Subjects With Renal Impairment
Non-cystic Fibrosis Bronchiectasis (NCFBE)
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
2 sites in 1 country: see every site and its status.
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.