Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Anlotinib
  • Angiogenesis
  • Antineoplastic Agents
  • Carcinoma
  • Carcinoma, Ovarian Epithelial
  • Endocrine System Diseases
  • Ovarian Diseases
  • Neoplasms, Glandular and Epithelial
  • Fallopian Tube Neoplasms
  • Genital Diseases, Female
  • Ovarian Neoplasms
  • Genital Neoplasms, Female
  • Neoplasms by Histologic Type
  • Neoplasms by Site
  • Tyrosine Kinase Inhibitor
Type
Interventional
Phase
Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Only males

Description

This study is a single-arm, multicenter, exploratory phase II study to observe the efficacy and safety of anlotinib combined with carboplatin/paclitaxel as first-line treatment in patients with advanced ovarian cancer. The primary end point are progression free survival; the secondary end points inc...

This study is a single-arm, multicenter, exploratory phase II study to observe the efficacy and safety of anlotinib combined with carboplatin/paclitaxel as first-line treatment in patients with advanced ovarian cancer. The primary end point are progression free survival; the secondary end points include objective response rate, disease control rate, overall survival and safety. The subjects in this study: patients with newly diagnosed advanced (FIGO stage III-IV) ovarian cancer, including histologically or pathologically confirmed high-grade serous ovarian cancer, fallopian tube cancer or primary peritoneal carcinoma

Tracking Information

NCT #
NCT04807166
Collaborators
Not Provided
Investigators
Study Chair: Wenjun Cheng, MD,PhD The First Affiliated Hospital with Nanjing Medical University