Non-Small Cell Lung CancerNCT07099027
The Lung Health Check Pilot
A study testing Low dose CT in people with Non-Small Cell Lung Cancer, run by Royal College of Surgeons, Ireland at 1 site in Ireland.
Trial summary
This study aims to test if it is feasible to introduce lung cancer screening in Ireland. People within a certain age group, who smoke or who smoked in the past, are at a greater risk of developing lung cancer. They can also develop chronic lung conditions that can affect their long-term health. Read more about this study
- Who is it for?
- Ages 55 to 74 yearsHealthy volunteers can take part
- Conditions the study is for
- Non-Small Cell Lung Cancer
- What is being tested?
- Low dose CT
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 2,183 participants
- Where
- 1 siteIreland
- Study dates
- 19 May 2025to 15 Jan 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 55 to 74 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- 55 - 74 years of age
- Current or former smokers
- Current: >100 cigarettes in lifetime and/or currently tobacco smoking
- Former: >100 cigarettes in lifetime and/or no tobacco smoking >= 28 days
- Referred from a GP for the LHC pilot
- PLCOM2012 ≥ 1.51% or LLPv2 ≥2.5% (Lung Cancer Risk Scores)
- Prostate Lung Cancer Colorectal Ovarian (PLCO) \& Liverpool Lung Project Version 2 (LLPv2)
Who cannot join
- Participant-reported history of chest CT in the last 12 months
- Inability to undergo non-contrast CT (e.g. >200 kg body weight, inability to lie flat)
- Participant reported known diagnosis of other advanced stage cancers
- Participant reported diagnosis of lung cancer of any stage in the last 5 years
- Likely non-compliance with study procedures, as determined by the participant i) Unable to provide informed consent ii) Inability to attend study visits
- Nursing home residents -
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Ireland1 site, 1 recruiting
- Recruiting
Beaumont RCSI Cancer Centre
Dublin
Sandra Roche, MD, 018093010 ext. 3010, lunghealthcheck@beaumont.ie
About this study
This study aims to test if it is feasible to introduce lung cancer screening in Ireland.
People within a certain age group, who smoke or who smoked in the past, are at a greater risk of developing lung cancer. They can also develop chronic lung conditions that can affect their long-term health. In Ireland, about 2,690 people are diagnosed with Lung Cancer every year. Unfortunately, 2 out of every 3 people diagnosed with lung cancer die per year.
Read more
The goal of this study is to try to screen for lung cancer in people before they have symptoms associated with the disease. We aim to do this by selecting people based on their age, whether they have smoked in the past or currently smoke as well as other relevant factors. People who take part in this study will have an assessment of how their lungs work and a low-dose CT scan. This is called a lung health check. The goal of the low-dose CT scan is to pick up lung cancer before it becomes symptomatic, and at an earlier stage. This scan uses a very low dose of radiation.
Unfortunately, without early detection, such as is the goal of this trial, 8 out of 10 people who go on to develop lung cancer will have advanced lung cancer when it is discovered, where outcomes tend to be poor. The earlier detection of lung cancer has a greater potential for treatment. Current international recommendations suggest carrying out these scans in the community rather than in a hospital. Therefore, we aim to deliver these lung health checks using a mobile unit in the community.
This study aims to test if we will successfully pick up lung cancer earlier by doing community-based 'lung health check's using mobile units in North Dublin and the North East, among people of a certain age and smoking history.
Read the detailed description
Lung Cancer Screening Lung cancer is the leading cause of cancer-related death in both men and women, and leads to more deaths from cancer than breast, colon and prostate cancer combined(4). When a patient presents symptomatically with lung cancer, this is typically associated with advanced disease and poor survival. Using low-dose CT scan as a method of early detection to identify lung cancer in an at risk population, has been shown to reduce lung cancer mortality by 20-26% in two large clinical trials across the USA and Europe (5,6). The National Lung Cancer Screening Trial (NLST) was launched in 2002 across 33 centres in the USA. In total, almost 54,000 eligible participants were randomised to non-contrast enhanced computed tomography (CT) of the chest for three years versus postero-anterior chest x-ray (CXR). Eligible participants were selected based on clinical criteria, including: age 55-79; >30 pack-year smoking history; <15 years abstinence if former smoker, no history of other life-threatening cancers; no recent haemoptysis or weight loss indicative of lung cancer; no prior chest CT in the past year. The study demonstrated high compliance with screening low-dose CT with >90% of participants attending each annual visit. The study demonstrated a 20.3% relative reduction in lung cancer mortality (247 versus 309) per 100,000 person years with low-dose CT versus CXR. There was also a significant reduction in all-cause mortality by 6.7%. Significantly, low-dose CT was also associated with a 7% risk of an invasive follow-up procedure which resulted in a false positive (4% with CXR). A separate European study (The NELSON trial) investigated the use of low-dose chest CT annually for four years versus no screening in a randomised clinical trial reported in 2020 (5). In this study, eligible participants had to have smoked >15 cigarettes per day for >25 years or >10 cigarettes a day for >30 years. Participants were excluded if any of the following criteria were met: current or past renal cell cancer, melanoma, breast cancer; treatment related to lung cancer in the past 5 years; or a chest CT in the past year. This study did not exclude participants based on age alone. Due to accrual challenges amongst females, the primary endpoint analysis focused on 13,195 men which were randomised in this study. A further 2,594 women were included in the study and their outcomes were analysed as a secondary endpoint. This study demonstrated a significant reduction in lung cancer mortality in the screening group (156 vs. 206, HR = 0.76, 95% CI = 0.61 - 0.94). The incidence of false positives in this study was low (n=264/22,600, 1.2%). In summary, two large randomised controlled trials have demonstrated that low-dose CT scans of the chest reduce lung-cancer related mortality in high-risk participants.
A review of evidence by public health experts has revealed significant issues with attendance and implementation of early detection programs internationally. Targets in the United Kingdom for Breast and Bowel screening can be as low as 70% and 50% respectively. Evidence from UK studies show that barriers to uptake in screening programmes include a perceived lack of access to screening programmes and, a fatalistic attitude to lung cancer screening in deprived communities(7). In the UKLS trial, McDonald et al noted that the likelihood of lung cancer risk increased with socioeconomic deprivation but conversely response rates and clinic attendance fell (8). Reducing barriers to participation is a critical challenge to the implementation of early detection of lung cancer.
Spirometry and Lung Health Questionnaire While the large scale US (NLST) and European trials (NELSON) have provided sufficient evidence to show clinical efficacy, poor uptake and economic costs of lung cancer screening have led to significant difficulties with implementation to date. Particular issues include encouraging high-risk participants from socio-economically deprived areas to participate. However, researchers and clinical implementation groups in the UK have been leading initiatives aimed at addressing these logistical and deliverability issues through the launching of numerous implementation pilot trials that have led to the creation of high quality, pragmatic and cost-effective programmes. These studies have invited more than 500,000 participants, scanned 120,000 (24%) participants and diagnosed 15,000 lung cancers since 2019. Their widespread success has led to a recommendation by the UK National Screening Committee (UKNSC) to introduce a national lung cancer screening programme in the UK in 2023.
A cornerstone of the UK approach is the implementation of community-based screening, which has been to significantly improve attendance in pilot studies. Location and access to a dedicated CT scanner is fundamental to the success of these programmes. Access to CT scanning in hospital-based settings is at a premium and in order to facilitate high-volume scanning in participants to be assessed, access to a dedicated screening specific CT scanner is required. The seminal example of a successful UK based pilot 15 that has driven much of the further developments in national community based testing has been The Manchester Lung Health Check (LHC) pilot. This involved a community initiative which invited participants via their primary care team(9). The pilot programme invited participants aged 55-74 years, whom were ever smokers and were living in defined catchment areas of socioeconomic disadvantage. This study also used a validated lung cancer risk prediction model - PLCO2012(10). This prediction model incorporated clinical factors such as age, smoking history, pulmonary disease, family history etc. To be eligible for inclusion, participants needed to have a predicted risk of lung cancer >1.51%. Critically, the programme involved a community engagement initiative whereby the research study team engaged with persons in community centres and local organisations in order to educate and enhance awareness of the proposed screening pilot. The pilot study demonstrated an uptake of 28.5 % with a total 2827 participants attending the pilot. Of these 2827 participants, 49% (1384/2827) were eligible for low dose CT (LDCT) and proceeded to screening. A total of 3% (n=42) lung cancers were detected in this screening programme. This evidence indicates that a service that could identify people at high risk of lung cancer and provide them with a LDCT scan, would lead to a reduction in deaths from lung cancer. In the Manchester screening trial, they performed a comparative analysis of the PLCO2012 and LLPv2. In this study, they discovered that the LLPv2 was more sensitive at identifying participants with lung cancer in a deprived population(10). For this reason, we will use both scoring models in our proposed study.
Another successful UK based lung cancer screening pilot, the Yorkshire Lung Screening Trial (YLST) involved randomisation of eligible participants aged 55-80 to telephone based lung cancer risk assessment versus usual care(11) . In this study, a total of 44,393 participants were invited with an initial response rate of 50.8%. Amongst the respondents, 34.4% of participants were eligible and 86.8% of those underwent screening (n=6819). In this study, authors used a remote lung cancer risk assessment (telephone based). They demonstrated that telephone based risk assessment is a feasible strategy for a lung cancer screening pilot.
Lung Disease is one of the leading causes of premature mortality in Ireland. Approximately 20% of all respiratory deaths occur as a result of Chronic Obstructive Pulmonary Disease (COPD). Unfortunately, accurate data for the incidence and prevalence of COPD in the Irish participants is not available. However, approximately 50% of lifelong smokers will develop COPD at some stage in their lives (12). Estimates suggest about 500,000 participants in Ireland may have COPD of whom 200,000 potentially have moderate and severe forms of disease. It is estimated that between 30-50% of these participants are currently undiagnosed. Late or underdiagnosed COPD is a significant health and health economic burden to the state with a strong association with hospital admissions for exacerbations. Approximately 30% of participants who present to hospital emergency departments with emergent COPD have had no formal diagnosis(13). Ireland also has the highest rate of hospital admission for COPD exacerbation in the OECD and the Beaumont Hospital catchment area has one of the highest rates of hospital admission for COPD exacerbation in the country at 376 admissions per 100,000 participants. The rate of decline in lung function is also faster in the earlier stages of the disease and therefore the potential for altering the course of the disease and improving outcomes is greater when identified earlier and when correct treatment interventions are initiated. Selected published lung cancer screening studies, where spirometry is performed, have shown that approximately 10-15% of lung cancer screening attendees have undiagnosed symptomatic COPD. As yet the data is unclear if routine spirometry improves health outcomes for lung cancer screening participants, but it is an area that warrants significant investigation and a Lung Health Check (LHC) environment is well-placed to enable such investigations. Spirometry may also help further stratify lung cancer risk in these participants as it acts as evidence of airway obstruction, which is an independent risk factor for the development of lung cancer.
Smoking Cessation Smoking cessation is an essential component of any lung cancer screening pilot trial or programme. The UKLS trial showed that lung cancer screening, particularly when associated with an abnormal scan result increases smoking cessation rates and represents a powerful opportunity to maximise smoking cessation rates. Cost-effectiveness data also shows that adding smoking cessation interventions is cost-effective, resulting in additional cancer deaths averted and life-years gained compared with screening alone. UK-based models of delivery advise that smoking cessation should be delivered by an opt-out approach, to reduce stigmatisation and should involve a co-located smoking cessation practitioner who is able to provide a comprehensive package of smoking cessation supports in an immediate fashion. UK policy advice suggests that consideration should be given to the use of Nicotine replacement therapy (NRT) as well as electronic cigarettes and vaping devices.
In summary, the evidence indicates that a service to identify people at high-risk of lung cancer and provide them with a low-dose chest CT scan would lead to a reduction in deaths from lung cancer. Equally, lung cancer screening is only effective with sufficient 16 uptake amongst high-risk participants. Experience internationally (e.g. Manchester LHC) would suggest the need for pilot studies to ensure adequate community engagement in lung cancer screening. We thus propose the first pilot study of lung cancer screening in Ireland, using a GP-referral mechanism, remote PLCO scoring, and attendance at a community-based LHC facility incorporating spirometry, smoking cessation and a low-dose CT scan of the chest.
The "Lung Health Check Pilot (LHC Pilot)" aims to provide a free low-dose CT scan to high-risk participants in an area with a high burden of lung cancer (North Dublin/North East Region). A pilot early detection program will be designed to minimise barriers to participation by:
- maximizing convenience through use of a community-based LHC/CT scan unit
- placing it strategically in a high prevalence area (North Dublin/North East Region) with high footfall or easy accessibility
- Incorporating supportive measures to maximise favourable outcomes in this participants through a respiratory assessment, and the incorporation of smoking cessation, as part of the LHC pilot.
We will also embed a translational research aims in this pilot study, to create a biorepository of breath and blood samples from participants to inform the next generation of lung cancer early detection methods and future prevention clinical trials through identification of non-invasive biomarkers.
High-risk participants (ever-smokers, aged 55-74 years) will be identified via GP practice databases and invited to undergo a 'lung health check'. As GP data is likely to be incomplete in this regard, invitations will be extended to all adults aged 55-74 years using low burden patient information leaflets and a dedicated invitation via an approved third-party vendor. These leaflets will be initially sent to each patient informing them of the pilot study, its benefits and who it is designed for. A formal letter of invitation will then be sent shortly after. Participants will be invited to participate via phonecall and letter. Participants who are invited to take part will be contacted via phoneline by qualified personnel, and asked an initial set of questions ensuring the participant is eligible to participate in the study based on the outlined inclusion and exclusion criteria (see section 2.6), and completion of their Validated PLCO (m2012) score (calculated cut-off point of 1.51%) and LLPv2 score (cut-off ≥2.5%). If they are eligible based on these assessments by phone, they will be invited to attend an in-person LHC at the community-based site, that includes a low dose CT chest(10) at a designated time. Those with a negative lung cancer risk assessment will be deemed not eligible to participate, and will be discharged from the programme via return letter. For those who attend the LHC, screening visits will be offered over two rounds, one year apart. Any identified pulmonary nodules on LHC performed CT will be analysed according to BTS pulmonary nodule guidelines and categorized as negative, indeterminate or positive. A case of suspected lung cancer (positive results) will require immediate referral to the local rapid access lung clinic, while indeterminate results will have an initial 3-month surveillance CT scan. CT reporting will be carried out by a group of radiologists with interest, expertise and training in Thoracic Oncology and BTS guidelines. Clinically-relevant incidental findings that require further clarification or work-up will be referred for GP or hospital specialist review and/or be discussed at a monthly dedicated Screening MDT in the Beaumont Hospital before deciding management plan. Some pulmonary nodules that need further discussion before follow-up planning will be discussed at this meeting also. The meeting will be attended by at a minimum: a respiratory Physician, a thoracic radiologist and the LHC programme manager.
The study will aim to 1) Explore the feasibility of a Lung Health Check (LHC) programme which incorporates a LDCT, respiratory disease assessment, and smoking cessation advice, in Ireland; 2) Identify the incidence, stage, treatment and outcomes of participants diagnosed with lung cancer in the high-risk participants; 3) Assess tobacco dependency of the high-risk participants with, reassessment after a community-based smoking cessation programme; 4) Define the proportion of participants with known or newly diagnosed respiratory disease and their management, as part of the LHC pilot; 5) Identify breath and blood-based biomarkers in participants; 6) Identify the optimal mechanism for the assessment eligibility for lung cancer screening in Ireland.
- Conditions
- Non-Small Cell Lung Cancer
- Being tested
- Low dose CT
- Keywords
- Screening, Lung cancer
- Medical subject headings
- Carcinoma, Non-Small-Cell Lung, Lung Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Low dose CTDiagnostic test
In this arm, participants will undergo a respiratory assessment, smoking cessation, low-dose CT and biospecimen for translational research.
| Study group | Role | What they receive |
|---|---|---|
| Lung Health Check | Experimental | In this arm, consented participants will undergo a 'Lung Health Check' which incorporates a respiratory disease assessment, smoking cessation, low-dose CT and collection of biospecimens for translational analyses. Receives: Diagnostic Test: Low dose CT |
What is being measured
The primary outcome is the main question the study is designed to answer.
i) The proportion of high-risk eligible participants aged 55-74 years who participate in a community-based lung health check ii)The proportion of individuals who consent to undergo telephone assessment
- Number of eligible participants who attend the LHC pilot after GP invitation/Number of high-risk participants invited via GP letter to the LHC pilot ii) Number of participants who consent to undergo telephone assessment/number of participants invite via GP letter to LHC pilot
Measured: 1 year
The proportion of individuals who consent to undergo telephone assessment
Number of individuals who consent to undergo telephone assessment/Number of individuals invited via GP letter to the LHC pilot ii) Number of participants who consent to undergo telephone assessment/number of participants invite via GP letter to LHC pilot
Measured: 1 year
Secondary outcomes (27)
The proportion of the participants (aged 55-74 years, from catchment area, who receive GP invitation) who attend a community-based initial (T0)LHC visit, and the mandated follow-up visit (T1)
The proportion of the participants (aged 55-74 years, from catchment area, who receive GP invitation) who attend a community-based initial (T0)LHC visit, and the mandated follow-up visit (T1)
Measured: 2 years
The proportion of participants (aged 55-74 years, from catchment area, who receive GP invitation) who attend a community-based T0 LHC visit, that are deemed eligible to participate based on eligibility criteria and risk scores
The proportion of participants (aged 55-74 years, from catchment area, who receive GP invitation) who attend a community-based T0 LHC visit, that are deemed eligible to participate based on eligibility criteria and risk scores
Measured: 1 year
The proportion of high-risk eligible participants aged 55-74 years for whom an appointment is booked in a community-based LHC visit
The proportion of high-risk eligible participants aged 55-74 years for whom an appointment is booked in a community-based LHC visit
Measured: 1 year
The proportion of high-risk participants that attend from an urban versus rural setting.
The proportion of high-risk participants that attend from an urban versus rural setting.
Measured: 1 year
The proportion of high-risk participants that respond to the LHC invitation and are deemed eligible by age, gender, socioeconomic status, social deprivation index, and presence of co-morbid conditions
The proportion of high-risk participants that respond to the LHC invitation and are deemed eligible by age, gender, socioeconomic status, social deprivation index, and presence of co-morbid conditions
Measured: 1 year
The proportion of high-risk participants that attend the LHC, by age, gender, socioeconomic status, social deprivation index, and presence of co-morbid conditions
The proportion of high-risk participants that attend the LHC, by age, gender, socioeconomic status, social deprivation index, and presence of co-morbid conditions
Measured: 1 year
The proportion of participants who attend the initial screening round who attend subsequent screening rounds (T0+3/T1)
The proportion of participants who attend the initial screening round who attend subsequent screening rounds (T0+3/T1)
Measured: 1 year
Number of participants referred to the Hospital Rapid Access Lung Cancer Clinic (RALCC) as a result of the LHC.
Number of participants referred to the Hospital Rapid Access Lung Cancer Clinic (RALCC) as a result of the LHC.
Measured: 3 years
Number of participants referred to the Beaumont Hospital Lung Cancer MDT as a result of the LHC.
Number of participants referred to the Beaumont Hospital Lung Cancer MDT as a result of the LHC.
Measured: 3 years
Proportion of participants that attend a LHC visit who are subsequently diagnosed with lung cancer.
Proportion of participants that attend a LHC visit who are subsequently diagnosed with lung cancer.
Measured: 3 years
Proportion of participants with lung cancer who are diagnosed with earlier stage lung cancer (stage I/II vs stage III/ IV), compared with national registry data on initial stage at diagnosis in the last 5 years.
Proportion of participants with lung cancer who are diagnosed with earlier stage lung cancer (stage I/II vs stage III/ IV), compared with national registry data on initial stage at diagnosis in the last 5 years.
Measured: 4 years
Proportion of participants diagnosed with lung cancer, who receive lung cancer treatment by modality and treatment intention (e.g. surgery, radiation therapy, systemic therapy; curative vs. palliative)
Proportion of participants diagnosed with lung cancer, who receive lung cancer treatment by modality and treatment intention (e.g. surgery, radiation therapy, systemic therapy; curative vs. palliative)
Measured: 3 years
The proportion of high-risk participants diagnosed with lung cancer who have a: i) PLCOm2012 ≥ 1.51% ii) LLPv2≥2.5%*
The proportion of high-risk participants diagnosed with lung cancer who have a:
- PLCOm2012 ≥ 1.51% ii) LLPv2 ≥2.5%*
Measured: 3 years
Number of participants with incidental findings identified on low-dose CT
Number of participants with incidental findings identified on low-dose CT
Measured: 4 years
Number of participants with newly diagnosed COPD from baseline spirometry and respiratory health questionnaires, complete as part of the LHC
Number of participants with newly diagnosed COPD from baseline spirometry and respiratory health questionnaires, complete as part of the LHC
Measured: 4 years
Nodule Detection Rate: The percentage of participants who have one or more nodules detected during the LHC (Nodule definition as per BTS Guidelines(1)
Nodule Detection Rate: The percentage of participants who have one or more nodules detected during the LHC (Nodule definition as per BTS Guidelines(1)
Measured: 4 years
Nodule Size: Nodule size for all nodules reported on T0 LHC CT
Nodule Size: Nodule size for all nodules reported on T0 LHC CT
Measured: 4 years
Nodule Growth Rate: For all patients with >1 CT scan and >=1 nodule. Growth rate will be defined and recorded. (Nodule Size at Follow-up CT/Nodule Size from CT at T0).
Nodule Growth Rate: For all patients with >1 CT scan and >=1 nodule. Growth rate will be defined and recorded. (Nodule Size at Follow-up CT/Nodule Size from CT at T0).
Measured: 4 years
False-Positive Rate: The percentage of participants who are investigated through RALCC for a suspicious nodule/suspected lung cancer that turns out to be non-malignant after investigation.
False-Positive Rate: The percentage of participants who are investigated through RALCC for a suspicious nodule/suspected lung cancer that turns out to be non-malignant after investigation.
Measured: 4 years
False-Negative Rate: The percentage of participants who are investigated through RALCC for a suspicious nodule/suspected lung cancer that turns out to be non-malignant after investigation.
False-Negative Rate: The percentage of participants who are investigated through RALCC for a suspicious nodule/suspected lung cancer that turns out to be non-malignant after investigation.
Measured: 4 years
Interval Cancer: a lung cancer diagnosed following a symptomatic presentation between screening rounds "outside screening,"
Interval Cancer: a lung cancer diagnosed following a symptomatic presentation between screening rounds "outside screening,"
Measured: 4 years
Sensitivity (True positive cases)
Sensitivity (True positive cases)
Measured: 4 years
Specificity (True-negative cases)
Specificity (True-negative cases)
Measured: 4 years
Referral rate: The percentage of participants referred for further investigation due to an incidental finding that requires medical assessment by either the participant's GP or a hospital specialist
Referral rate: The percentage of participants referred for further investigation due to an incidental finding that requires medical assessment by either the participant's GP or a hospital specialist
Measured: 4 years
Identify participant smoking rates before and after a brief smoking intervention followed by opt-out referral to HSE led community-based smoking cessation programme for current smokers, as part of the LHC.
Identify participant smoking rates before and after a brief smoking intervention followed by opt-out referral to HSE led community-based smoking cessation programme for current smokers, as part of the LHC.
Measured: 4 years
Proportion of participants who participate in the HSE led opt-out smoking cessation programme, after participation in the LHC pilot.
Proportion of participants who participate in the HSE led opt-out smoking cessation programme, after participation in the LHC pilot.
Measured: 4 years
1-year smoking cessation rates at T1 vs. T0 timepoints.
1-year smoking cessation rates at T1 vs. T0 timepoints.
Measured: 4 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Aug 2025
- Study start19 May 2025
- Primary completion15 Feb 2026 (estimated)
- Study completion15 Jan 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Non-Small Cell Lung CancerStudies 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Screening
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 2,183 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Royal College of Surgeons, Ireland
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Jarushka Naidoo, MD, Principal investigator, Beaumont RCSI Cancer Centre
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07099027
- Sponsor's protocol ID
- LHC Pilot
- Status last verified
- May 2025
- First submitted
- 6 May 2025
- Last updated
- 1 Aug 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
O Reilly D, Roche S, Noonan C, O'Shea J, Toomey S, Hennessy BT, Fitzmaurice GJ, Egan K, Dunne J, Dowling CM, Counihan I, O'Brien E, Sulaiman I, Morgan R, Jacob B, Baird AM, Cotter S, Bailey D, Maguire G, Bennett K, Sorensen J, Healy NA, Ryan J, Redmond P, Ryan DJ, Naidoo J. Lung Health Check pilot: Ireland's flagship lung cancer screening trial. BMJ Open Respir Res. 2025 Sep 10;12(1):e003035. doi: 10.1136/bmjresp-2024-003035.
PubMed 40935563
Study at a glance
From the registry record, last updated by the sponsor on 1 Aug 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Lung Health Check Pilot
- ClinicalTrials.gov ID
- NCT07099027
- Acronym / sponsor ID
- LHC Pilot
- Conditions
- Non-Small Cell Lung Cancer
- Keywords
- Screening, Lung cancer
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 2,183 participants (estimated)
- Lead sponsor
- Royal College of Surgeons, IrelandUniversity, hospital or other
- Study start
- 19 May 2025 (actual)
- Primary completion
- 15 Feb 2026 (estimated)
- Study completion
- 15 Jan 2028 (estimated)
- First posted
- 1 Aug 2025 (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.
This study aims to test if it is feasible to introduce lung cancer screening in Ireland.
People within a certain age group, who smoke or who smoked in the past, are at a greater risk of developing lung cancer. They can also develop chronic lung conditions that can affect their long-term health. In Ireland, about 2,690 people are diagnosed with Lung Cancer every year. Unfortunately, 2 out of every 3 people diagnosed with lung cancer die per year.
The goal of this study is to try to screen for lung cancer in people before they have symptoms associated with the disease. We aim to do this by selecting people based on their age, whether they have smoked in the past or currently smoke as well as other relevant factors. People who take part in this study will have an assessment of how their lungs work and a low-dose CT scan. This is called a lung health check. The goal of the low-dose CT scan is to pick up lung cancer before it becomes symptomatic, and at an earlier stage. This scan uses a very low dose of radiation.
Unfortunately, without early detection, such as is the goal of this trial, 8 out of 10 people who go on to develop lung cancer will have advanced lung cancer when it is discovered, where outcomes tend to be poor. The earlier detection of lung cancer has a greater potential for treatment. Current international recommendations suggest carrying out these scans in the community rather than in a hospital. Therefore, we aim to deliver these lung health checks using a mobile unit in the community.
This study aims to test if we will successfully pick up lung cancer earlier by doing community-based 'lung health check's using mobile units in North Dublin and the North East, among people of a certain age and smoking history.
Detailed description
Lung Cancer Screening Lung cancer is the leading cause of cancer-related death in both men and women, and leads to more deaths from cancer than breast, colon and prostate cancer combined(4). When a patient presents symptomatically with lung cancer, this is typically associated with advanced disease and poor survival. Using low-dose CT scan as a method of early detection to identify lung cancer in an at risk population, has been shown to reduce lung cancer mortality by 20-26% in two large clinical trials across the USA and Europe (5,6). The National Lung Cancer Screening Trial (NLST) was launched in 2002 across 33 centres in the USA. In total, almost 54,000 eligible participants were randomised to non-contrast enhanced computed tomography (CT) of the chest for three years versus postero-anterior chest x-ray (CXR). Eligible participants were selected based on clinical criteria, including: age 55-79; >30 pack-year smoking history; <15 years abstinence if former smoker, no history of other life-threatening cancers; no recent haemoptysis or weight loss indicative of lung cancer; no prior chest CT in the past year. The study demonstrated high compliance with screening low-dose CT with >90% of participants attending each annual visit. The study demonstrated a 20.3% relative reduction in lung cancer mortality (247 versus 309) per 100,000 person years with low-dose CT versus CXR. There was also a significant reduction in all-cause mortality by 6.7%. Significantly, low-dose CT was also associated with a 7% risk of an invasive follow-up procedure which resulted in a false positive (4% with CXR). A separate European study (The NELSON trial) investigated the use of low-dose chest CT annually for four years versus no screening in a randomised clinical trial reported in 2020 (5). In this study, eligible participants had to have smoked >15 cigarettes per day for >25 years or >10 cigarettes a day for >30 years. Participants were excluded if any of the following criteria were met: current or past renal cell cancer, melanoma, breast cancer; treatment related to lung cancer in the past 5 years; or a chest CT in the past year. This study did not exclude participants based on age alone. Due to accrual challenges amongst females, the primary endpoint analysis focused on 13,195 men which were randomised in this study. A further 2,594 women were included in the study and their outcomes were analysed as a secondary endpoint. This study demonstrated a significant reduction in lung cancer mortality in the screening group (156 vs. 206, HR = 0.76, 95% CI = 0.61 - 0.94). The incidence of false positives in this study was low (n=264/22,600, 1.2%). In summary, two large randomised controlled trials have demonstrated that low-dose CT scans of the chest reduce lung-cancer related mortality in high-risk participants.
A review of evidence by public health experts has revealed significant issues with attendance and implementation of early detection programs internationally. Targets in the United Kingdom for Breast and Bowel screening can be as low as 70% and 50% respectively. Evidence from UK studies show that barriers to uptake in screening programmes include a perceived lack of access to screening programmes and, a fatalistic attitude to lung cancer screening in deprived communities(7). In the UKLS trial, McDonald et al noted that the likelihood of lung cancer risk increased with socioeconomic deprivation but conversely response rates and clinic attendance fell (8). Reducing barriers to participation is a critical challenge to the implementation of early detection of lung cancer.
Spirometry and Lung Health Questionnaire While the large scale US (NLST) and European trials (NELSON) have provided sufficient evidence to show clinical efficacy, poor uptake and economic costs of lung cancer screening have led to significant difficulties with implementation to date. Particular issues include encouraging high-risk participants from socio-economically deprived areas to participate. However, researchers and clinical implementation groups in the UK have been leading initiatives aimed at addressing these logistical and deliverability issues through the launching of numerous implementation pilot trials that have led to the creation of high quality, pragmatic and cost-effective programmes. These studies have invited more than 500,000 participants, scanned 120,000 (24%) participants and diagnosed 15,000 lung cancers since 2019. Their widespread success has led to a recommendation by the UK National Screening Committee (UKNSC) to introduce a national lung cancer screening programme in the UK in 2023.
A cornerstone of the UK approach is the implementation of community-based screening, which has been to significantly improve attendance in pilot studies. Location and access to a dedicated CT scanner is fundamental to the success of these programmes. Access to CT scanning in hospital-based settings is at a premium and in order to facilitate high-volume scanning in participants to be assessed, access to a dedicated screening specific CT scanner is required. The seminal example of a successful UK based pilot 15 that has driven much of the further developments in national community based testing has been The Manchester Lung Health Check (LHC) pilot. This involved a community initiative which invited participants via their primary care team(9). The pilot programme invited participants aged 55-74 years, whom were ever smokers and were living in defined catchment areas of socioeconomic disadvantage. This study also used a validated lung cancer risk prediction model - PLCO2012(10). This prediction model incorporated clinical factors such as age, smoking history, pulmonary disease, family history etc. To be eligible for inclusion, participants needed to have a predicted risk of lung cancer >1.51%. Critically, the programme involved a community engagement initiative whereby the research study team engaged with persons in community centres and local organisations in order to educate and enhance awareness of the proposed screening pilot. The pilot study demonstrated an uptake of 28.5 % with a total 2827 participants attending the pilot. Of these 2827 participants, 49% (1384/2827) were eligible for low dose CT (LDCT) and proceeded to screening. A total of 3% (n=42) lung cancers were detected in this screening programme. This evidence indicates that a service that could identify people at high risk of lung cancer and provide them with a LDCT scan, would lead to a reduction in deaths from lung cancer. In the Manchester screening trial, they performed a comparative analysis of the PLCO2012 and LLPv2. In this study, they discovered that the LLPv2 was more sensitive at identifying participants with lung cancer in a deprived population(10). For this reason, we will use both scoring models in our proposed study.
Another successful UK based lung cancer screening pilot, the Yorkshire Lung Screening Trial (YLST) involved randomisation of eligible participants aged 55-80 to telephone based lung cancer risk assessment versus usual care(11) . In this study, a total of 44,393 participants were invited with an initial response rate of 50.8%. Amongst the respondents, 34.4% of participants were eligible and 86.8% of those underwent screening (n=6819). In this study, authors used a remote lung cancer risk assessment (telephone based). They demonstrated that telephone based risk assessment is a feasible strategy for a lung cancer screening pilot.
Lung Disease is one of the leading causes of premature mortality in Ireland. Approximately 20% of all respiratory deaths occur as a result of Chronic Obstructive Pulmonary Disease (COPD). Unfortunately, accurate data for the incidence and prevalence of COPD in the Irish participants is not available. However, approximately 50% of lifelong smokers will develop COPD at some stage in their lives (12). Estimates suggest about 500,000 participants in Ireland may have COPD of whom 200,000 potentially have moderate and severe forms of disease. It is estimated that between 30-50% of these participants are currently undiagnosed. Late or underdiagnosed COPD is a significant health and health economic burden to the state with a strong association with hospital admissions for exacerbations. Approximately 30% of participants who present to hospital emergency departments with emergent COPD have had no formal diagnosis(13). Ireland also has the highest rate of hospital admission for COPD exacerbation in the OECD and the Beaumont Hospital catchment area has one of the highest rates of hospital admission for COPD exacerbation in the country at 376 admissions per 100,000 participants. The rate of decline in lung function is also faster in the earlier stages of the disease and therefore the potential for altering the course of the disease and improving outcomes is greater when identified earlier and when correct treatment interventions are initiated. Selected published lung cancer screening studies, where spirometry is performed, have shown that approximately 10-15% of lung cancer screening attendees have undiagnosed symptomatic COPD. As yet the data is unclear if routine spirometry improves health outcomes for lung cancer screening participants, but it is an area that warrants significant investigation and a Lung Health Check (LHC) environment is well-placed to enable such investigations. Spirometry may also help further stratify lung cancer risk in these participants as it acts as evidence of airway obstruction, which is an independent risk factor for the development of lung cancer.
Smoking Cessation Smoking cessation is an essential component of any lung cancer screening pilot trial or programme. The UKLS trial showed that lung cancer screening, particularly when associated with an abnormal scan result increases smoking cessation rates and represents a powerful opportunity to maximise smoking cessation rates. Cost-effectiveness data also shows that adding smoking cessation interventions is cost-effective, resulting in additional cancer deaths averted and life-years gained compared with screening alone. UK-based models of delivery advise that smoking cessation should be delivered by an opt-out approach, to reduce stigmatisation and should involve a co-located smoking cessation practitioner who is able to provide a comprehensive package of smoking cessation supports in an immediate fashion. UK policy advice suggests that consideration should be given to the use of Nicotine replacement therapy (NRT) as well as electronic cigarettes and vaping devices.
In summary, the evidence indicates that a service to identify people at high-risk of lung cancer and provide them with a low-dose chest CT scan would lead to a reduction in deaths from lung cancer. Equally, lung cancer screening is only effective with sufficient 16 uptake amongst high-risk participants. Experience internationally (e.g. Manchester LHC) would suggest the need for pilot studies to ensure adequate community engagement in lung cancer screening. We thus propose the first pilot study of lung cancer screening in Ireland, using a GP-referral mechanism, remote PLCO scoring, and attendance at a community-based LHC facility incorporating spirometry, smoking cessation and a low-dose CT scan of the chest.
The "Lung Health Check Pilot (LHC Pilot)" aims to provide a free low-dose CT scan to high-risk participants in an area with a high burden of lung cancer (North Dublin/North East Region). A pilot early detection program will be designed to minimise barriers to participation by:
- maximizing convenience through use of a community-based LHC/CT scan unit
- placing it strategically in a high prevalence area (North Dublin/North East Region) with high footfall or easy accessibility
- Incorporating supportive measures to maximise favourable outcomes in this participants through a respiratory assessment, and the incorporation of smoking cessation, as part of the LHC pilot.
We will also embed a translational research aims in this pilot study, to create a biorepository of breath and blood samples from participants to inform the next generation of lung cancer early detection methods and future prevention clinical trials through identification of non-invasive biomarkers.
High-risk participants (ever-smokers, aged 55-74 years) will be identified via GP practice databases and invited to undergo a 'lung health check'. As GP data is likely to be incomplete in this regard, invitations will be extended to all adults aged 55-74 years using low burden patient information leaflets and a dedicated invitation via an approved third-party vendor. These leaflets will be initially sent to each patient informing them of the pilot study, its benefits and who it is designed for. A formal letter of invitation will then be sent shortly after. Participants will be invited to participate via phonecall and letter. Participants who are invited to take part will be contacted via phoneline by qualified personnel, and asked an initial set of questions ensuring the participant is eligible to participate in the study based on the outlined inclusion and exclusion criteria (see section 2.6), and completion of their Validated PLCO (m2012) score (calculated cut-off point of 1.51%) and LLPv2 score (cut-off ≥2.5%). If they are eligible based on these assessments by phone, they will be invited to attend an in-person LHC at the community-based site, that includes a low dose CT chest(10) at a designated time. Those with a negative lung cancer risk assessment will be deemed not eligible to participate, and will be discharged from the programme via return letter. For those who attend the LHC, screening visits will be offered over two rounds, one year apart. Any identified pulmonary nodules on LHC performed CT will be analysed according to BTS pulmonary nodule guidelines and categorized as negative, indeterminate or positive. A case of suspected lung cancer (positive results) will require immediate referral to the local rapid access lung clinic, while indeterminate results will have an initial 3-month surveillance CT scan. CT reporting will be carried out by a group of radiologists with interest, expertise and training in Thoracic Oncology and BTS guidelines. Clinically-relevant incidental findings that require further clarification or work-up will be referred for GP or hospital specialist review and/or be discussed at a monthly dedicated Screening MDT in the Beaumont Hospital before deciding management plan. Some pulmonary nodules that need further discussion before follow-up planning will be discussed at this meeting also. The meeting will be attended by at a minimum: a respiratory Physician, a thoracic radiologist and the LHC programme manager.
The study will aim to 1) Explore the feasibility of a Lung Health Check (LHC) programme which incorporates a LDCT, respiratory disease assessment, and smoking cessation advice, in Ireland; 2) Identify the incidence, stage, treatment and outcomes of participants diagnosed with lung cancer in the high-risk participants; 3) Assess tobacco dependency of the high-risk participants with, reassessment after a community-based smoking cessation programme; 4) Define the proportion of participants with known or newly diagnosed respiratory disease and their management, as part of the LHC pilot; 5) Identify breath and blood-based biomarkers in participants; 6) Identify the optimal mechanism for the assessment eligibility for lung cancer screening in Ireland.
Study design
- Primary purpose
- Screening
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Lung Health Check | Experimental | Diagnostic Test: Low dose CTIn this arm, consented participants will undergo a 'Lung Health Check' which incorporates a respiratory disease assessment, smoking cessation, low-dose CT and collection of biospecimens for translational analyses. |
Who may qualify
- Ages
- 55 to 74 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- 55 - 74 years of age
- Current or former smokers
- Referred from a GP for the LHC pilot
- PLCOM2012 ≥ 1.51% or LLPv2 ≥2.5% (Lung Cancer Risk Scores)
Key exclusion criteria (6 listed)
- Participant-reported history of chest CT in the last 12 months
- Inability to undergo non-contrast CT (e.g. >200 kg body weight, inability to lie flat)
- Participant reported known diagnosis of other advanced stage cancers
- Participant reported diagnosis of lung cancer of any stage in the last 5 years
- Likely non-compliance with study procedures, as determined by the participant i) Unable to provide informed consent ii) Inability to attend study visits
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Low dose CTIn this arm, participants will undergo a respiratory assessment, smoking cessation, low-dose CT and biospecimen for translational research. | Diagnostic test | Lung Health Check |
Primary outcome
i) The proportion of high-risk eligible participants aged 55-74 years who participate in a community-based lung health check ii)The proportion of individuals who consent to undergo telephone assessment
Time frame: 1 year
i) Number of eligible participants who attend the LHC pilot after GP invitation/Number of high-risk participants invited via GP letter to the LHC pilot ii) Number of participants who consent to undergo telephone assessment/number of participants invite via GP letter to LHC pilot
The proportion of individuals who consent to undergo telephone assessment
Time frame: 1 year
Number of individuals who consent to undergo telephone assessment/Number of individuals invited via GP letter to the LHC pilot ii) Number of participants who consent to undergo telephone assessment/number of participants invite via GP letter to LHC pilot
27 secondary outcomes
The proportion of the participants (aged 55-74 years, from catchment area, who receive GP invitation) who attend a community-based initial (T0)LHC visit, and the mandated follow-up visit (T1)
Time frame: 2 years
The proportion of participants (aged 55-74 years, from catchment area, who receive GP invitation) who attend a community-based T0 LHC visit, that are deemed eligible to participate based on eligibility criteria and risk scores
Time frame: 1 year
The proportion of high-risk eligible participants aged 55-74 years for whom an appointment is booked in a community-based LHC visit
Time frame: 1 year
The proportion of high-risk participants that attend from an urban versus rural setting.
Time frame: 1 year
The proportion of high-risk participants that respond to the LHC invitation and are deemed eligible by age, gender, socioeconomic status, social deprivation index, and presence of co-morbid conditions
Time frame: 1 year
The proportion of high-risk participants that attend the LHC, by age, gender, socioeconomic status, social deprivation index, and presence of co-morbid conditions
Time frame: 1 year
The proportion of participants who attend the initial screening round who attend subsequent screening rounds (T0+3/T1)
Time frame: 1 year
Number of participants referred to the Hospital Rapid Access Lung Cancer Clinic (RALCC) as a result of the LHC.
Time frame: 3 years
Number of participants referred to the Beaumont Hospital Lung Cancer MDT as a result of the LHC.
Time frame: 3 years
Proportion of participants that attend a LHC visit who are subsequently diagnosed with lung cancer.
Time frame: 3 years
Proportion of participants with lung cancer who are diagnosed with earlier stage lung cancer (stage I/II vs stage III/ IV), compared with national registry data on initial stage at diagnosis in the last 5 years.
Time frame: 4 years
Proportion of participants diagnosed with lung cancer, who receive lung cancer treatment by modality and treatment intention (e.g. surgery, radiation therapy, systemic therapy; curative vs. palliative)
Time frame: 3 years
The proportion of high-risk participants diagnosed with lung cancer who have a: i) PLCOm2012 ≥ 1.51% ii) LLPv2≥2.5%*
Time frame: 3 years
Number of participants with incidental findings identified on low-dose CT
Time frame: 4 years
Number of participants with newly diagnosed COPD from baseline spirometry and respiratory health questionnaires, complete as part of the LHC
Time frame: 4 years
Nodule Detection Rate: The percentage of participants who have one or more nodules detected during the LHC (Nodule definition as per BTS Guidelines(1)
Time frame: 4 years
Nodule Size: Nodule size for all nodules reported on T0 LHC CT
Time frame: 4 years
Nodule Growth Rate: For all patients with >1 CT scan and >=1 nodule. Growth rate will be defined and recorded. (Nodule Size at Follow-up CT/Nodule Size from CT at T0).
Time frame: 4 years
False-Positive Rate: The percentage of participants who are investigated through RALCC for a suspicious nodule/suspected lung cancer that turns out to be non-malignant after investigation.
Time frame: 4 years
False-Negative Rate: The percentage of participants who are investigated through RALCC for a suspicious nodule/suspected lung cancer that turns out to be non-malignant after investigation.
Time frame: 4 years
Interval Cancer: a lung cancer diagnosed following a symptomatic presentation between screening rounds "outside screening,"
Time frame: 4 years
Sensitivity (True positive cases)
Time frame: 4 years
Specificity (True-negative cases)
Time frame: 4 years
Referral rate: The percentage of participants referred for further investigation due to an incidental finding that requires medical assessment by either the participant's GP or a hospital specialist
Time frame: 4 years
Identify participant smoking rates before and after a brief smoking intervention followed by opt-out referral to HSE led community-based smoking cessation programme for current smokers, as part of the LHC.
Time frame: 4 years
Proportion of participants who participate in the HSE led opt-out smoking cessation programme, after participation in the LHC pilot.
Time frame: 4 years
1-year smoking cessation rates at T1 vs. T0 timepoints.
Time frame: 4 years
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Aug 2025.
- Derived from this study: PubMed 40935563O Reilly D, Roche S, Noonan C, O'Shea J, Toomey S, Hennessy BT, Fitzmaurice GJ, Egan K, Dunne J, Dowling CM, Counihan I, O'Brien E, Sulaiman I, Morgan R, Jacob B, Baird AM, Cotter S, Bailey D, Maguire G, Bennett K, Sorensen J, Healy NA, Ryan J, Redmond P, Ryan DJ, Naidoo J. Lung Health Check pilot: Ireland's flagship lung cancer screening trial. BMJ Open Respir Res. 2025 Sep 10;12(1):e003035. doi: 10.1136/bmjresp-2024-003035.
- Lung Heath Check websiteLink provided by the sponsor.
- Individual participant dataSharing planned: No
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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.
Jarushka Naidoo, MD principal investigator
Beaumont RCSI Cancer Centre
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Low dose CT in people with Non-Small Cell Lung Cancer, run by Royal College of Surgeons, Ireland at 1 site in Ireland.
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 7 inclusion and 6 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: looking for participants now, as of the sponsor's last update on 1 Aug 2025. 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 Ireland. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Sandra Roche, PhD (018093010 ext. 3010, lunghealthcheck@beaumont.ie), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
i) The proportion of high-risk eligible participants aged 55-74 years who participate in a community-based lung health check ii)The proportion of individuals who consent to undergo telephone assessment (time frame: 1 year). 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?
On the ClinicalTrials.gov record for NCT07099027, 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 1 Aug 2025.