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A real-world study of a combination regimen based on irinotecan hydrochloride liposome injection (II) for colorectal cancer

A real-world study of a combination regimen based on irinotecan hydrochloride liposome injection (II) for colorectal cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100483
Enrollment
Unknown
Registered
2025-04-10
Start date
2025-04-15
Completion date
Unknown
Last updated
2025-04-14

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

Conditions

Colorectal cancer

Interventions

Observation group:None

Sponsors

Panzhihua Hospital of Integrated Chinese and Western Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. All subjects voluntarily participated in the study and signed informed consent; 2. 18 years old =70g/L; b) neutrophil count (ANC) >=1.5×109/L; c) platelet count (PLT) >=75×109/L. (2) Liver function tests should meet the following criteria: a) alanine aminotransferase (ALT) =12 weeks; 8. Patients who had not participated in other clinical trials within 4 weeks before enrollment; 9. Investigator assessment of patients who could use irinotecan hydrochloride liposome injection (II).

Exclusion criteria

Exclusion criteria: 1.Pregnant or lactating women; 2.Presence of a severe active infection? (> Grade 2 CTCAE5.0), or autoimmune disease?; 3.Patients with brain metastases; 4.patients are known to be allergic to any component of the test drug; 5.Patients who have had any cancer other than colorectal cancer prior to the start of the study treatment. Exceptions include cervical carcinoma in situ, cured basal cell carcinoma, and thyroid papillary carcinoma; 6.Severe cardiovascular and cerebrovascular diseases; 7.Vulnerable groups, including people with mental illness, people with cognitive impairment, critically ill patients, minors, pregnant women, etc; 8.The researchers determined that other conditions were not suitable for inclusion in the study;

Design outcomes

Primary

MeasureTime frame
Adverse events;

Secondary

MeasureTime frame
Progression free Survival;Overall Survival;Objective response rate;

Countries

China

Contacts

Public ContactLei Xiaolin

Panzhihua Hospital of Integrated Chinese and Western Medicine

2428086827@qq.com+86 812 2213442

Outcome results

None listed

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