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NCT06349837

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

Recruiting now Phase 1 Last updated 17 December 2025
What this trial tests

Phase 1 trial testing Tislelizumab in Solid Tumor in 24 participants. Currently enrolling.

Timeline
18 April 2024
Primary endpoint
31 March 2026
30 November 2026

Quick facts

Lead sponsorSichuan University
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment24
Start date18 April 2024
Primary completion31 March 2026
Estimated completion30 November 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Sichuan University

Who can join

18 and older, any sex, with Solid Tumor. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Low-dose radiotherapy remodels the tumor immune microenvironment via the cGAS-STING pathway: mechanisms, challenges, and combination therapy strategies.
    He Y, Zeng X, Liu Q, Zhou L, et al · · 2026 · PMID 41803899 · DOI 10.1186/s12943-026-02634-5

Verify or expand the search:

Other trials of Tislelizumab

Trials testing the same drug.

Other recruiting trials for Solid Tumor

Currently open trials in the same condition.

Other Sichuan University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06349837.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing