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Liposomal irinotecan in Chinese patients with advanced pancreatic cancer: a prospective, multi-center, observational real-world study

Liposomal irinotecan in Chinese patients with advanced pancreatic cancer: a prospective, multi-center, observational real-world study

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300078041
Enrollment
Unknown
Registered
2023-11-27
Start date
2023-12-01
Completion date
Unknown
Last updated
2023-12-03

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

Conditions

pancreatic cancer

Interventions

Cohort 1, Experimental group (liposome irinotecan-based regimens (first-line therapy)):NA
Cohort 1, Control group (AG regimen (first-line therapy)):NA
Cohort 2 (liposome irinotecan-based regimens (second-line therapy)):NA

Sponsors

Fudan University Shanghai Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patient is 18 years or older; 2.Histologically or cytologically proven pancreatic cancer; 3.Confirmed unresectable disease in a multidisciplinary consultation meeting; 4.Eastern Cooperative Oncology Group performance status score of 0~2; 5.Has a life expectancy of = 3 months; 6.Patient has signed informed consent and is willing to comply with the protocol.

Exclusion criteria

Exclusion criteria: 1.Complicated with uncontrollable systemic diseases (such as unstable angina pectoris, myocardial infarction, congestive heart failure, severe unstable ventricular arrhythmia, severe pericardial disease history, and other cardiovascular diseases; uncontrolled hypertension, diabetes, etc.); 2.Known allergies or intolerance to therapeutic drugs or their excipients; 3.Patients who are participating in other interventional clinical trials; 4.Have other malignant tumors requiring treatment; 5.Patient inappropriate for entry into this study judged by the Investigator.

Design outcomes

Primary

MeasureTime frame
Progress-free survival;

Secondary

MeasureTime frame
Overall response rate;Overall survival;Safety;

Countries

China

Contacts

Public ContactXianjun Yu

Fudan University Shanghai Cancer Center

yuxianjun@fudanpci.org+86 21 6403 1446

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026