~8 spots leftby Apr 2026

Cabozantinib or Paclitaxel in Treating Patients With Persistent or Recurrent Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cavity Cancer

Recruiting in Palo Alto (17 mi)
+172 other locations
UA
Overseen byUrsula A Matulonis
Age: 18+
Sex: Female
Travel: May Be Covered
Time Reimbursement: Varies
Trial Phase: Phase 2
Waitlist Available
Sponsor: National Cancer Institute (NCI)
No Placebo Group
Prior Safety Data
Breakthrough Therapy

Trial Summary

What is the purpose of this trial?

This randomized phase II trial studies how well giving cabozantinib-s-malate or paclitaxel works in treating patients with persistent or recurrent epithelial ovarian, fallopian tube, or primary peritoneal cavity cancer. Cabozantinib-s-malate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. It is not yet known whether cabozantinib-s-malate or paclitaxel is more effective at treating patients with persistent or recurrent epithelial ovarian, fallopian tube, or primary peritoneal cavity cancer.

Research Team

UA

Ursula A Matulonis

Principal Investigator

NRG Oncology

Eligibility Criteria

Inclusion Criteria

Patients must have recurrent or persistent epithelial ovarian, fallopian tube or primary peritoneal carcinoma; histologic documentation of the original primary tumor is required via the pathology report
Measurable disease is defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded); each lesion must be greater than or equal to 10 mm when measured by computed tomography (CT), magnetic resonance imaging (MRI) or caliper measurement by clinical exam; or greater than or equal to 20 mm when measured by chest x-ray; lymph nodes must be greater than or equal to 15 mm in short axis when measured by CT or MRI
Ascites and/or pleural effusion attributed to tumor Solid and/or cystic abnormalities on radiographic imaging that do not meet RECIST 1.1 definitions for target lesions
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Treatment Details

Interventions

  • Cabozantinib S-malate (Tyrosine Kinase Inhibitor)
  • Paclitaxel (Mitotic Inhibitor)
Participant Groups
2Treatment groups
Experimental Treatment
Group I: Arm II (paclitaxel)Experimental Treatment2 Interventions
Patients receive paclitaxel IV over 1 hour on days 1, 8, and 15.
Group II: Arm I (cabozantinib-s-malate)Experimental Treatment2 Interventions
Patients receive cabozantinib-s-malate PO QD on days 1-28.

Find a Clinic Near You

Research Locations NearbySelect from list below to view details:
Rush University Medical CenterChicago, IL
Associates In Womens HealthWichita, KS
Indiana University/Melvin and Bren Simon Cancer CenterIndianapolis, IN
McFarland Clinic PC-MarshalltownMarshalltown, IA
More Trial Locations
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Who Is Running the Clinical Trial?

National Cancer Institute (NCI)

Lead Sponsor

Trials
14080
Patients Recruited
41,180,000+