RecruitingPhase 3NCT07251582
Effect of Infusion Timing on Pathologic Response to Neoadjuvant Immunotherapy in Resectable Non-Small Cell Lung Cancer
Studying NON RARE IN EUROPE: Non-small cell lung cancer
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Hunan Province Tumor Hospital
- Intervention
- Time of Day-based Assignment for Infusion of Immune Checkpoint Inhibitor (e.g., toripalimab, or pembrolizumab) + platinum-based chemotherapy(other)
- Enrollment
- 156 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2025 – 2029
Study locations (2)
- Hunna Cancer Hospital, Clinical Trails Center, Changsha, Hunan, China
- Hunan Cancer hospital, Changsha, Hunan, China
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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