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Study identifier: NCT06488950 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study of TIL in Advanced Solid Tumors (DFGD)

Condition: Advanced Solid Tumor · Tumor Infiltrating Lymphocytes · Treatment Side Effects  ·  Sponsor: Shanghai Juncell Therapeutics

PhaseEARLY_Phase 1
Planned participants30
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This study is to investigate the safety and efficacy of tumor infiltrating lymphocyte (TIL) therapy in patients with advanced solid tumors. Autologous TILs and gene-edited TILs are expanded from tumor resections or biopsies and infused i.v. into the patient after NMA lymphodepletion treatment with hydroxychloroquine(600mg,single-dose) and cyclophosphamide.

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

Talk to the study team

GC Clinical  ·  086-18001759113  ·  clinicaltrials@juncell.com

Always discuss trial participation with your own doctor first.

Locations (1)

Third Affiliated Hospital of Naval Medical UniversityShanghai, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06488950