Survey of Brigatinib for treating non-small cell lung cancer
Official title: General Use-results Survey of Alunbrig Tablets "Non-small Cell Lung Cancer"
Run by Takeda · NCT05100069 · Data updated 2026-11-12
This study looks at how safe Brigatinib is for Japanese patients with non-small cell lung cancer while they take the medication as part of their regular treatment.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | Takeda Industry-sponsored |
| Drugs / interventions | birigatinib, Brigatinib |
| Locations | 1 site (Tokyo) |
| Status | Recruiting |
| Started | November 1, 2021 |
| Main results expected | September 30, 2030 |
| Study ends | September 30, 2030 |
| Registry record updated | March 17, 2026 |
| Trial ID | NCT05100069 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are individuals with unresectable advanced or recurrent ALK fusion gene-positive non-small cell lung cancer.
✕Probably not a fit
Patients with a history of hypersensitivity to any component of Brigatinib may not benefit from this study.
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 surveys the use of Brigatinib tablets in Japanese patients with non-small cell lung cancer. Participants will take Brigatinib according to their clinic's standard practices, while the study monitors for any side effects related to lung disease over a period of one year. The study is sponsored by Takeda, which will provide guidelines for clinics on how to record patient outcomes. The focus is on understanding the safety profile of Brigatinib in this specific patient population.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the safety and side effects of Brigatinib, improving treatment protocols for patients with non-small cell lung cancer.
How similar studies have gone: While this study is observational and focuses on safety, similar studies have previously shown success in understanding the effects of targeted therapies in lung cancer.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion criteria Participants with unresectable advanced/recurrent ALK fusion gene-positive non-small cell lung cancer. Exclusion criteria Participants who has a history of hypersensitivity to any component of birigatinib.
Where it's running
-
Takeda Selected Site
Tokyo, Japan Recruiting
Study contacts
- Study coordinator: Takeda Contact
- Email: medinfoUS@takeda.com
- Phone: +1-877-825-3327
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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.