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Efficacy and Safety of Nab-Paclitaxel /Carboplatin for First-Line Chemotherapy of Advanced Ovarian Cancer

Efficacy and Safety of Nab-Paclitaxel /Carboplatin for First-Line Chemotherapy of Advanced Ovarian Cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034944
Enrollment
Unknown
Registered
2020-07-25
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-07-27

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

Conditions

Ovarian Cancer

Interventions

experimental group:Nab-Paclitaxel plus Carboplatin
control group:Paclitaxel plus Carboplatin

Sponsors

the First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Aged >= 18 years , = 1.5*10^9/L, Platelet count >= *10^9/L, Hemoglobin >= 9.0 g/dL; Adequate liver function indicated by all of the following: Serum bilirubin = 40 mL/min. 6) Patients with >= 1 measurable disease; 7) Signed Informed Consent Form.

Exclusion criteria

Exclusion criteria: 1) There is brain metastasis; 2) Uncontrolled severe medical conditions that the investigator believes will affect the subject's treatment with the study protocol: Dementia, change of mental state or any mental illness that would prevent understanding or informed consent or the completion of a questionnaire; 3) A history of allergy or hypersensitivity to any therapeutic ingredient; 4) Malignant tumors other than OV within 5 years, except basal cell or squamous cell skin cancer that is adequately treated, and ductal carcinoma in situ after radical surgery; 5) Subjects with peripheral neuropathy >=2 according to CTCAE V 5.0; 6) HBsAg positive subjects with peripheral blood HBV DNA titer >=1x10^3 IU/mL; 7) Hepatitis C virus (HCV) antibody positive or human immunodeficiency virus (HIV) antibody positive; 8) Received systemic or surgical treatment for OV; 9) Has been treated with any other experimental drug or participated in another interventional clinical trial within 30 days of the screening period; 10) The researcher thinks it is not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Objective Remission Rate (ORR);

Secondary

MeasureTime frame
Progress Free Survival (PFS);Quanlity of Life (QoL);

Countries

China

Contacts

Public ContactLiu Ziling

Cancer Center, the First Hospital of Jilin University

drzilingliu@163.com+86 13943001600

Outcome results

None listed

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