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A non-interventional registration study of bevacizumab biological analogues in China patients with advanced solid tumor

A non-interventional registration study of bevacizumab biological analogues in China patients with advanced solid tumor

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300075824
Enrollment
Unknown
Registered
2023-09-15
Start date
2023-07-06
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

solid tumor

Interventions

Bevacizumab treatment group :None

Sponsors

Tianjin Cancer Hospital Airport Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Voluntarily agree to participate in the study and sign the informed consent; 2. The patient was confirmed by histopathologically /cytopathological as malignant solid tumor (including non-small cell lung cancer, colorectal cancer, cervical cancer, ovarian cancer, liver cancer, brain glioma); 3. Age =18 years old; 4. The investigators determined that the patient could receive bevacizumab alone or in combination treatment .

Exclusion criteria

Exclusion criteria: 1. Patients who are participating in other blind trials; 2. There is evidence that the patient is a pregnant or lactating woman; 3. The investigator believes that the patient is not suitable to participate in this study for any other conditions.

Design outcomes

Primary

MeasureTime frame
Safety;

Secondary

MeasureTime frame
Other occasional or rare adverse events;

Countries

China

Contacts

Public ContactDong Wang

Tianjin Cancer Hospital Airport Hospital

tzkgyx@163.com+86 153 3202 8676

Outcome results

None listed

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