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Clinical Trial Summary

The purpose of this study is to compare the efficacy and safety of nab-paclitaxel with solvent-based taxanes as first-line treatment for patients with advanced primary epithelial ovarian cancer (EOC), primary peritoneal carcinoma or fallopian tube carcinoma.


Clinical Trial Description

One of the major challenges related to solvent-based taxanes administration in clinical practice is the high rate of hypersensitivity reactions (HSRs). Nab-paclitaxel has showed its considerable survival and low toxicity profiles in first-line treatment for several solid tumors and is recommended as a treatment for recurrent epithelial ovarian cancer (EOC). We focus on clinical efficacy and safety outcomes of nab-paclitaxel in current clinical studies of primary EOC treatment and aim to explore the potential feasibility of nab-paclitaxel as the first-line treatment for EOC, primary peritoneal carcinoma or fallopian tube carcinoma. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05737303
Study type Interventional
Source Women's Hospital School Of Medicine Zhejiang University
Contact Yaxia Chen, MD
Phone +86-571-87061501
Email chenyax@zju.edu.cn
Status Recruiting
Phase Phase 3
Start date February 24, 2023
Completion date December 31, 2027