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Real-world data on the safety of immune-checkpoint inhibitors

Real-world data on the safety of immune-checkpoint inhibitors

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300075974
Enrollment
Unknown
Registered
2023-09-20
Start date
2023-11-30
Completion date
Unknown
Last updated
2023-09-26

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

Conditions

malignancy

Interventions

Immune checkpoint inhibitors treatment group:None

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 200 Years

Inclusion criteria

Inclusion criteria: (1) Patients diagnosed with malignant tumors by pathology, including solid tumors and hematological tumors; (2) Have used ICIs at least once; (3) The clinical medical records are complete and reliable, with complete efficacy evaluation results, adverse reaction records, and survival follow-up data.

Exclusion criteria

Exclusion criteria: Patients with incomplete clinical data

Design outcomes

Primary

MeasureTime frame
Incidence of adverse events;

Secondary

MeasureTime frame
The incidence of serious adverse events;Postoperative complication rate;hospitalization days after operation;survival time;Baseline data of patients;

Countries

China

Contacts

Public ContactJinhan he

Department of Pharmacy, West China Hospital, Sichuan University

jinhanhe@scu.edu.cn+86 189 8060 5932

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 9, 2026