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Study identifier: NCT06349837 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Safety and Tolerability of LDRT Plus Concurrent Partial SBRT and Tislelizumab in Patients With Bulky Tumors

Condition: Solid Tumor  ·  Sponsor: Sichuan University

PhasePhase 1
Planned participants24
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a 3+3 dose escalation phase I study which aims to evaluate the safety and tolerability of low dose radiotherapy (LDRT) plus concurrent partial Stereotactic Ablative Radiotherapy (SBRT) and Tislelizumab in Patients with bulky tumors who have failed standard therapy. At least 9 participants will be enrolled in this study.

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

Talk to the study team

Ren Luo, MD  ·  18349337131  ·  luorenbu@163.com

Li Li, BA  ·  02885424619  ·  tracy.li_2010@hotmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

West China Hospital, Sichuan UniversityChengdu, Sichuan, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06349837