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Study identifier: NCT06936748 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

SFRT+Sequential Hypofractionated/Conventional Fractionated RT+Iparomlimab and Tuvonralimab for Relapsed/Refractory Solid Tumors

Condition: Cancer  ·  Sponsor: Second Affiliated Hospital of Nanchang University

PhasePhase 2
Planned participants30
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

Study Objectives Primary Objective:To evaluate the safety of SFRT followed by hypofractionated/conventional fractionated radiotherapy combined with Iparomlimab and Tuvonralimab Injection in relapsed/refractory bulky solid tumors. Secondary Objectives:To assess efficacy (objective response rate, disease control rate, progression-free survival, etc.) and identify predictive biomarkers.To explore correlations between immunologic biomarkers (e.g., PD-L1 expression, plasma IL-2/IL-10) and treatment outcomes. Study Endpoints Primary: Safety (incidence/severity of treatment-related adverse events). Secondary: ORR, DCR, DoR, mPFS, mOS Exploratory: Biomarker analysis (PD-L1, IL-2, IL-10).

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

Talk to the study team

Anwen Liu, Ph.D.  ·  +8613767120022  ·  awliu666@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

The Second Affiliated Hospital of Nanchang UniversityNanchang, Jiangxi, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06936748