Overview
FOLFOX/FOLFIRI Containing Levofolinic Acid (Zuoyu ®) in the Treatment of Unresectable or Metastatic Colorectal Cancer
Status:
Recruiting
Recruiting
Trial end date:
2024-12-01
2024-12-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
To observe and evaluate the efficacy and safety of FOLFOX/FOLFIRI± target-directed regimen containing Levofolinic Acid (Zuoyu ®) in first-line treatment of unresectable or metastatic colorectal cancerPhase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
China Medical University, China
Criteria
Inclusion Criteria:- Male or female, ≥18 years old;
- Patients with histopathologically confirmed unresectable or metastatic colorectal
cancer who have not previously received chemotherapy or targeted therapy for
unresectable or metastatic lesions;
- Have at least one measurable lesion according to RECIST 1.1 standards;
- ECOG PS score: 0-2;
- Expected survival greater than 3 months;
- Routine blood routine, liver and kidney function, electrocardiogram and other routine
tests were basically normal, no contraindications of chemotherapy;
- The subjects voluntarily joined the study, signed the informed consent, had good
compliance, and cooperated with follow-up visits;
- Researchers believe treatment can benefit.
Exclusion Criteria:
- A proven allergy to the test drug and/or its excipients;
- Pregnant or lactating women;
- Patients judged by the investigator to be unsuitable for inclusion in this study;