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A parallel, randomized, controlled phase III clinical trial comparing the efficacy and safety of regorafenib and furquintinib in the third line treatment of colorectal cancer

A parallel, randomized, controlled phase III clinical trial comparing the efficacy and safety of regorafenib and furquintinib in the treatment of colorectal cancer

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040543
Enrollment
Unknown
Registered
2020-12-01
Start date
2020-12-01
Completion date
Unknown
Last updated
2021-03-08

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

Conditions

Colorectal cancer

Interventions

Furquitinib group:Furquitinib

Sponsors

Maoming people's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Male or female, older than 18 years; 2.PS 0-2; 3. Colorectal cancer confirmed by histology or cytology has received first-line and second-line chemotherapy, whether or not treatment with bevacizumab or cetuximab; 4. The life expectancy is more than 12 weeks; 5. Sign informed consent; 6. There are measurable tumor lesions in imaging; 7. Be able to comply with the research and follow-up procedures.

Exclusion criteria

Exclusion criteria: 1. Any unstable systemic disease (including active infection, poorly controlled hypertension, unstable angina, congestive heart failure, liver, kidney or metabolic disease); 2. Before treatment, he received regorafenib and furquintinib for systematic anti-tumor treatment; 3. Patients who are unable to accept oral administration, need intravenous high-energy nutrition, have undergone surgery affecting absorption before, or have active peptic ulcer; 4. Lactating women; 5. Granulocyte count is less than 1.5 * 10^9/L, platelet count is less than 75 * 10^9/L; 6. Serum bilirubin >1.5 ULN; 7. AST and ALT >2 ULN, and >5 ULN in case of liver metastasis; Serum creatinine >1.5 ULN, or creatinine clearance rate was less than 50 ml/min.

Design outcomes

Primary

MeasureTime frame
Progression free survival;

Secondary

MeasureTime frame
Objective response rate;

Countries

China

Contacts

Public ContactYisheng Huang

Maoming people's Hospital

hysd0760@163.com+86 13719211288

Outcome results

None listed

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