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Clinical study of apatinib mesylate in the treatment of platinum resistant recurrent ovarian cancer

Clinical study of apatinib mesylate in the treatment of platinum resistant recurrent ovarian cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800016108
Enrollment
Unknown
Registered
2018-05-11
Start date
2018-05-10
Completion date
Unknown
Last updated
2018-05-14

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

Conditions

ovarian cancer

Interventions

Case series:apatinib

Sponsors

First Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Women older than eighteen and sign ICF; 2. ECOG 0-2; 3. Estimated survival time=3 mouths; 4. Ovarian epithelial carcinoma diagnosed by pathology or histology; 5. The time of last chemotherapy is more than 4 weeks; 6. The damage caused by other treatments was restored,the interval between nitroso or mitomycin is more than 6 weeks; 7. Other cytotoxic drugs, radiotherapy or surgery were accepted for more than 4 weeks, and the wounds healed completely; 8. The main organs (liver, kidney and heart) function basically normal.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. High blood pressure and failure to be reduced to normal range by antihypertensive drugs(Systolic pressure > 140 mmHg, diastolic pressure >90mmHg); 3. Variety of factors affecting oral drugs (such as inability to swallow, chronic diarrhea, and intestinal obstruction); 4. Coagulopathy (INR>1.5×ULN APTT>1.5×ULN), with Bleeding tendency; 5. Urinary protein is more than + + and confirmed the 24 hour urinary protein quantitative>1g; 6. Received apatinib or other VEGFR inhibitors, such as bevacizumab, Solafinib, Sunitinib; 7. Metastases of the central nervous system with symptoms; 8. Other cases the researchers judged that could affect the outcome of the clinical study.

Design outcomes

Primary

MeasureTime frame
ORR;

Secondary

MeasureTime frame
PFS;OS;

Countries

China

Contacts

Public ContactZhiping Liu

First Affiliated Hospital of Harbin Medical University

824387905@qq.com+86 13936034546

Outcome results

None listed

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