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A Study to Evaluate the Efficacy and Safety of a First-line Treatment for Advanced Colorectal Cancer With Simultaneous Infusion of Levozolinate for Injection and 5-FU

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Phase II study of simultaneous infusion of levozolinate for injection and 5-FU as first-line treatment for advanced colorectal cancer

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
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• The subjects voluntarily joined this study and signed the informed consent form.

• Age: 18 to 75 years old, gender not limited;

• ECOG PS score: 0-2 points

• Patients with unresectable or metastatic colorectal cancer confirmed by histology or cytology, where the primary tumor location and the status of RAS and BRAF are known;

• No previous treatment for unresectable or metastatic lesions has been received;

• There is at least one measurable lesion in accordance with the RECIST 1.1 standard;

• In the pre-treatment examination indicators, there was no serious hematopoietic function abnormality, and the functions of the heart, lungs, liver and kidneys were basically normal.

‣ Hemoglobin (Hb) ≥70 g/L;

⁃ White blood cell count (WBC) ≥3.0×109/L; Neutrophil count (NEUT) ≥1.5×109/L;

⁃ Platelet count (PLT) ≥100×109/L;

⁃ Liver function (aspartate aminotransferase AST or alanine aminotransferase ALT) level ≤2.5 times the upper limit of normal value (ULN); Renal function (serum creatinine sCr) level ≤1.5 times the upper limit of the normal value (ULN). Total bilirubin (TBIL) ≤1.5 times the upper limit of the normal value (ULN).

• The expected survival period is more than three months.

Locations
Other Locations
China
Chinese PLA General Hospital, Beijing
RECRUITING
Beijing
Contact Information
Primary
Guanghai Dai
daigh301@vip.sina.com
+861066947252
Backup
miaomiao Gou
daigh301@vip.sina.com
Time Frame
Start Date: 2025-05-15
Estimated Completion Date: 2029-12
Participants
Target number of participants: 583
Treatments
Experimental: arm1
For patients with wild-type RAS and BRAF and the primary lesion located in the left colorectum, the mFOLFOX6 or FOLFIRI regimens with simultaneous infusion of levofolinic acid and 5-FU for injection were received. Whether to combine cetuximab was determined by the researchers
Experimental: arm2
For patients with both RAS and BRAF wild-type and with the primary lesion located in the right colorectal and/or RAS or BRAF mutant type, the mFOLFOX6 or FOLFIRI regimen with simultaneous infusion of levofolinic acid and 5-FU for injection, whether to combine bevacizumab, was determined by the researchers
Related Therapeutic Areas
Sponsors
Leads: Chinese PLA General Hospital

This content was sourced from clinicaltrials.gov