Tislelizumab use in European patients with NSCLC or ES-SCLC in routine care
Official title: A Real-World Evaluation of Tislelizumab Treatment Patterns and Effectiveness in European Patients With Resectable or Advanced Non-Small Cell Lung Cancer and Small Cell Lung Cancer
Run by BeOne Medicines · NCT07652736 · Data updated 2026-11-12
This study looks at how tislelizumab is used in real-world European patients with advanced NSCLC or extensive-stage SCLC and what outcomes are seen in everyday clinical practice.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 440 (estimated) |
| Sponsor | BeOne Medicines Industry-sponsored |
| Drugs / interventions | tislelizumab |
| Locations | 6 sites (Córdoba and 5 other locations) |
| Status | Recruiting |
| Started | June 5, 2026 |
| Main results expected | November 15, 2027 |
| Study ends | November 17, 2030 |
| Registry record updated | October 15, 2026 |
| Trial ID | NCT07652736 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Patients with advanced NSCLC or extensive-stage SCLC who are receiving tislelizumab as part of routine clinical practice in the participating European centers.
✕Probably not a fit
Patients who do not receive clinical benefit from tislelizumab or who are not treated with tislelizumab as part of standard care may not contribute to observed benefits.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study collects real-world data on treatment patterns and outcomes for patients with advanced NSCLC or extensive-stage SCLC who receive tislelizumab as part of standard care in Europe. Data will come from routine clinical practice across several hospitals and will reflect how the drug is used outside of controlled trials. The goal is to describe how patients fare on tislelizumab in real-world settings and to identify patterns that may inform future care. The study does not assign treatments or change medical decisions; it observes treatments already chosen by treating physicians. Results may help clinicians understand where tislelizumab fits in current practice and generate hypotheses for future research.
Why it matters
Potential benefit: If successful, the study could clarify real-world effectiveness and usage patterns of tislelizumab in European patients.
How similar studies have gone: Prior real-world data on tislelizumab and similar PD-1 inhibitors in lung cancer have informed practice, though this study focuses on routine European use and may be more exploratory.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants are eligible to be included in the study only if they meet all the following criteria: 1. Participants or their legal representative must sign written inform consent form (ICF) 2. Participants receive tislelizumab as part of routine clinical practice as determined by the treating physician per standard of care and in accordance with the SmPC, within the approved indications in the 4 cohorts described. Note: The decision to treat the patient with a tislelizumab-based regimen, as per its authorized indication, must have been made by the treating physician prior to and independent of the patient's consideration for participation in this study. Exclusion Criteria: * Participants are excluded from the study if they meet any of the following criteria: 1. Participants who are unable to understand all implications of study participation. 2. Participants who have contraindications for treatment with tislelizumab in the investigator's opinion or have any contraindication as listed in the SmPC of tislelizumab. 3. Participants who are deemed ineligible according to the investigator's opinion and the SmPC of tislelizumab.
Where it's running
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Hospital Universitario Reina Sofía
Córdoba, Spain Recruiting -
Hospital Universitario de Jaén
Jaén, Spain Recruiting -
Hospital Universitario Lucus Augusti (HULA)
Lugo, Spain Recruiting -
Hospital de Segovia
Segovia, Spain Recruiting -
Hospital General de Segovia
Segovia, Spain Recruiting -
Hospital de Sagunto
Valencia, Spain Recruiting
Study contacts
- Study coordinator: Study Director
- Email: clinicaltrials@beonemed.com
- Phone: 1-877-828-5568
Similar studies
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.