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The phase ? study of Apatinib in treating patients with advanced/recurrent ovarian cancer

The phase ? study of Apatinib in treating patients with advanced/recurrent ovarian cancer

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIC-17010304
Enrollment
Unknown
Registered
2017-01-01
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

ovarian cancer

Interventions

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. female patients with age of 18–70 years old; 2. histologically confirmed cervical squamous cell carcinoma or epithelial ovarian carcinoma; 3. Computed tomography, magnetic resonance image or positron emission tomography confirmed advanced or recurrent disease; 4. had at least three lines of chemotherapy fail before participating in the study and at least 4 weeks after last chemotherapy; 5. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1; 6. at least one measurable lesion according to Response Evaluation Criteria In Solid Tumors (RECIST) 1.1 criteria; (?) Appropriate hematologic, coagulation, hepatic and renal function (hemoglobin = 90g/L, platelet > 80 x 10^9/L, neutrophil count > 1.5 x 10^9/L, serum creatinine =1x upper limit of normal (ULN), bilirubin =1.25 x ULN, ) international normalized ratio (INR) =1.5, and activated partial thromboplastin time (APTT) < 1.5 x ULN).

Exclusion criteria

Exclusion criteria: 1. pregnant or lactating female patients; 2. prior history of other malignancies or antiangiogenic therapy; 3. uncontrolled high blood pressure with medication (> 140/90 mmHg); 4. receiving thrombolytics or anticoagulants therapy; 5. existing active bleeding, ulcer, intestinal perforation, intestinal obstruction, unhealed wound or fracture; 6. urine protein = 2+ or 24 hours total urinary protein > 1.0 g; 7. simultaneously receiving any anti-tumor therapy; 8. less than 4 weeks after last clinical trial; 9. symptomatic central nervous system metastases or carcinomatous meningitis; 10. suffering severe pulmonary or cardiac disease.

Design outcomes

Primary

MeasureTime frame
progression free survival;

Secondary

MeasureTime frame
Overall survival;Disease control rates;Objective response rate;

Countries

China

Contacts

Public ContactXie Congying

The First Affiliated Hospital of Wenzhou Medical University

wzxiecongying@163.com+86 13867711881

Outcome results

None listed

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