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A real world study of the first bevacizumab biological analogue in China (Ankeda) in patients with Colorectal cancer field

A real world study of the first bevacizumab biological analogue in China (Ankeda) in patients with Colorectal cancer field

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000039865
Enrollment
Unknown
Registered
2020-11-12
Start date
2020-11-20
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

Colorectal cancer

Interventions

Case series:Nil

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Diagnosed as colorectal cancer by histopathology; 2. ECOG score 0-2 points; 3. Need to receive Ankeda drug therapy (single drug or combination therapy).

Exclusion criteria

Exclusion criteria: 1. Patients with severe bleeding or recent hemoptysis (>=1/2 teaspoon of fresh blood); 2. Patients with uncontrolled hypertension and hypertensive crisis; 3. Those who are planning to undergo major traumatic surgery within 4 weeks before administration, or during the study period, or whose wounds are not fully healed within 4 weeks before administration; 4. Patients who have a perforation or fistula of the digestive tract in the past, or who have experienced a perforation or fistula after using bevacizumab; 5. Women who are pregnant or breastfeeding, and men and women who refuse to take effective contraceptive measures.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate;

Countries

China

Contacts

Public ContactHaiping Zheng

Department of Oncology, the First Affiliated Hospital of Guangxi Medical University

zhenghaiping@163.com+86 13878862418

Outcome results

None listed

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