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A real-world study of toripalimab in the treatment of advanced solid tumor patients in China

A real-world study of toripalimab in the treatment of advanced solid tumor patients in China

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121488
Enrollment
Unknown
Registered
2026-03-31
Start date
2026-04-02
Completion date
Unknown
Last updated
2026-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Driver gene negative non-small cell lung cancer, urothelial carcinoma, esophageal cancer, nasopharyngeal carcinoma, melanoma, renal cell carcinoma, small cell lung cancer, triple-negative breast cancer, hepatocellular carcinoma, renal cell carcinoma, small cell lung cancer, triple-negative breast cancer, hepatocellular carcinoma

Interventions

Toripalimab experimental group:None

Sponsors

Yantai Yuhuangding Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Pathologically or cytologically confirmed as the corresponding solid tumor (driver gene-negative non-small cell lung cancer, urothelial carcinoma, esophageal cancer, nasopharyngeal carcinoma, melanoma, renal cell carcinoma, small cell lung cancer, triple-negative breast cancer, hepatocellular carcinoma); 2. Based on the TNM stage being advanced (TXNXM1), or the locally advanced stage applicable for systemic treatment; 3. There is at least one lesion that can be evaluated by CT or MRI; 4. Patients who have completed at least 3 cycles of toripalimab monotherapy and/or combination therapy; 5. At least one effectiveness assessment (imaging assessment 6 to 12 weeks after the first administration) has been completed; 6. The subjects voluntarily joined this study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Having suffered from other malignant tumors within the past five years, except for localized tumors that have been cured through research. 2. Patients who participated in other clinical trials during the observation period; 3. This study is a real-world one and there are no special exclusion criteria.

Design outcomes

Primary

MeasureTime frame
Objective response rate;

Secondary

MeasureTime frame
Overall survival;Progression-free survival;

Countries

China

Contacts

Public ContactCheng Yu

Yantai Yuhuangding Hospital

Liubaodong123@yeah.net+86 535 6691999

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026