EPO906 Therapy in Patients With Advanced Ovarian, Primary Fallopian, or Primary Peritoneal Cancer

Completed · Phase 2

Conditions studied: Ovarian Neoplasms, Peritoneal Neoplasms, Fallopian Tube Neoplasms

In brief

This study will examine whether the new investigational drug EPO906, given by intravenous infusion (IV directly into the vein), is effective in shrinking tumors and preventing the growth of cells that cause ovarian, fallopian, or peritoneal cancers. Recruitment in the United States is complete but the study is still enrolling in other countries.

Key facts

Study ID

NCT00035100

Run by

Novartis Pharmaceuticals

People needed

54

Starts

2001-09-01

Last updated by the study team

2012-04-16

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• The following patients may be eligible for the study:
• Histologically or cytologically documented evidence of ovarian, primary Fallopian or primary peritoneal cancer with at least one measurable lesion (if previous radiation treatment, the target lesion must have demonstrated progression since the radiation)
• Must have a life expectancy of greater than three (3) months
• Prior failure to respond following front-line treatment with a taxane and platinum (or a combination therapy) may be eligible.

You may not qualify if…

• The following patients are not eligible for the study:
• Patients with radiation therapy or chemotherapy within the last four weeks
• Patients who have had any chemotherapy not containing a taxane and platinum for their disease
• Patients with borderline ovarian and macropapillary tumors
• Patients with unresolved bowel obstruction
• Patients with symptomatic CNS metastases or leptomeningeal involvement
• Patients with any peripheral neuropathy or unresolved diarrhea greater than Grade 1
• Patients with severe cardiac insufficiency
• Patients taking Coumadin or other warfarin-containing agents with the exception of low dose Coumadin (1 mg or less) for the maintenance of in-dwelling lines or ports
• History of another malignancy within 5 years prior to study entry except curatively treated non-melanoma skin cancer or cervical cancer in situ
• Patients with active or suspected acute or chronic uncontrolled infection including abcesses or fistulae
• HIV+ patients
• Pregnant or lactating females.

Where it is running

• Novartis Investigative Site — New Brunswick, New Jersey, United States
• Novartis Investigative Site — Toronto, Ontario, Canada
• Novartis Investigative Site — Enschede, Netherlands, Netherlands
• Novartis Investigative Site — Amsterdam, Netherlands
• Novartis Investigative Site — Zwolle, Netherlands
• Novartis Investigative Site — Bratislava, Slovakia
• Novartis Investigative Site — Košice, Slovakia
• Novartis Investigative Site — Surrey, United Kingdom

Full record on ClinicalTrials.gov

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