← Back to Clinical Trials
Recruiting NCT05100069

NCT05100069 Survey of Brigatinib Used To Treat People With Non-Small Cell Lung Cancer

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT05100069
Status Recruiting
Phase
Sponsor Takeda
Condition Non-small Cell Lung Cancer (NSCLC)
Study Type OBSERVATIONAL
Enrollment 500 participants
Start Date 2021-11-01
Primary Completion 2030-09-30

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Brigatinib

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 500 participants in total. It began in 2021-11-01 with a primary completion date of 2030-09-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study is a survey in Japan of Brigatinib tablets used to treat Japanese people with non-small cell lung cancer. The study sponsor will not be involved in how the participants are treated but will provide instructions on how the clinics will record what happens during the study. The main aim of the study is to check for side effects related to lung disease from Brigatinib. During the study, participants with non-small cell lung cancer will take Brigatinib tablets according to their clinic's standard practice. The study doctors will check for side effects from Brigatinib for 1 year.

Eligibility 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.

Contact & Investigator

Central Contact

Takeda Contact

✉ medinfoUS@takeda.com

📞 +1-877-825-3327

Principal Investigator

Study Director

STUDY DIRECTOR

Takeda

Frequently Asked Questions

Who can join the NCT05100069 clinical trial?

This trial is open to participants of all sexes, studying Non-small Cell Lung Cancer (NSCLC). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05100069 currently recruiting?

Yes, NCT05100069 is actively recruiting participants. Contact the research team at medinfoUS@takeda.com for enrollment information.

Where is the NCT05100069 trial being conducted?

This trial is being conducted at Tokyo, Japan.

Who is sponsoring the NCT05100069 clinical trial?

NCT05100069 is sponsored by Takeda. The principal investigator is Study Director at Takeda. The trial plans to enroll 500 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology