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A Prospective, Open label, Single-arm Clinical Trail to Evaluate the Safety and Efficacy of Apatinib MesylateTablets in Advanced Epithelial Ovarian Cancer failing to respond to Second-line Chemotherapy

A Prospective, Open label, Single-arm Clinical Trail to Evaluate the Safety and Efficacy of Apatinib MesylateTablets in Advanced Epithelial Ovarian Cancer failing to respond to Second-line Chemotherapy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-16008034
Enrollment
Unknown
Registered
2016-03-01
Start date
2016-03-01
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

Epithelial Ovarian Cancer

Interventions

Case series:Apatinib MesylateTablets 500mg or 750mg(depend on BSA) Qd

Sponsors

Changhai Hospital Affiliated to The Second Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Epithelial ovarian carcinoma diagnosed by histologic or cytological test; 2. Aged 18 to 75 years; 3. Recurrent after standard treatment or no respond to chemotherapy; 4. 0-2 scores of Eastern Cooperative Oncology Group (ECOG); 5. an estimated life expectancy of at least 3 months; 6. HB>=90g/L, ANC>=1.5×10^9/L, PLT>=80×10^9/L; 7. adequate liver and kidney function.

Exclusion criteria

Exclusion criteria: 1. severe hypertension; 2. Have the disease influencing oral drug absorption, such as unable to swallow, chronic diarrhea and intestinal obstruction; 3. contraindications for Apatinib MesylateTablets; 4. mental disease; 5. allergies to any components of the study drug; 6. concurrent any other clinical and biochemical test.

Design outcomes

Primary

MeasureTime frame
ORR(Objective Response Rate);DCR(Disease Control Rate);

Secondary

MeasureTime frame
Quality of Life;Ovarian cancer symptoms;

Countries

China

Contacts

Public ContactChaoqin Yu
chqyu81@163.com+86 13818390984

Outcome results

None listed

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