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Study identifier: NCT06809764 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Clinical Effectiveness and Safety of Trastuzumab Deruxtecan (T-DXd) in Chinese Patients With HER2m NSCLC (RERUN)

Condition: Non-small Cell Lung Cancer  ·  Sponsor: Daiichi Sankyo

PhaseN/A
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Trastuzumab deruxtecan (T-DXd) is an approved therapy for non-small cell lung cancer (NSCLC) in China. Despite the clinical trial evidence, there is no real-world data of T-DXd used in Chinese lung cancer patients with HER2 mutations. This real world, prospective study will assess the effectiveness and safety of T-DXd in patients with locally advanced or metastatic, HER2 mutation-positive NSCLC in real-world setting.

This description comes directly from the study's public registry record.

Talk to the study team

Contact for Clinical Trial Information  ·  908-992-6400  ·  CTRinfo_us@daiichisankyo.com

Always discuss trial participation with your own doctor first.

Locations (23)

Cancer Hospital Chinese Academy of Medical SciencesBeijing, ChinaNot Yet Recruiting
Peking University International HospitalBeijing, ChinaNot Yet Recruiting
Beijing Cancer HospitalBeijing, ChinaNot Yet Recruiting
Hunan Second People's HospitalChangsha, ChinaNot Yet Recruiting
Fujian Cancer HospitalFuzhou, ChinaNot Yet Recruiting
Affiliated Cancer Hospital and Institute of Guangzhou Medical UniversityGuangzhou, ChinaNot Yet Recruiting
The First Affiliated Hospital of Sun Yat-sen UniversityGuangzhou, ChinaNot Yet Recruiting
Zhejiang Cancer HospitalHangzhou, ChinaNot Yet Recruiting
Anhui Provincial Cancer HospitalHefei, ChinaNot Yet Recruiting
First Affiliated Hospital of Shandong First Medical UniversityJinan, ChinaNot Yet Recruiting
Cancer Hospital of Shandong First Medical UniversityJinan, ChinaNot Yet Recruiting
The First Affiliated Hospital of Jinzhou Medical UniversityJinzhou, ChinaNot Yet Recruiting

+ 11 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06809764