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Clinical Trials/NCT00964626
NCT00964626
Unknown
Phase 2

A Phase II Study of Efficacy and Safety of Paclitaxel and Cisplatin Every 2 Weeks as the First-line Treatment of Patients With Ovarian Cancer Stage Ic-IV.

Russian Academy of Medical Sciences1 site in 1 country60 target enrollmentApril 2009

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Ovarian Cancer
Sponsor
Russian Academy of Medical Sciences
Enrollment
60
Locations
1
Primary Endpoint
Progression-free survival
Last Updated
12 years ago

Overview

Brief Summary

RATIONALE: Drugs used in chemotherapy, such as paclitaxel and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells.

PURPOSE: This phase II trial is studying the side effects of giving paclitaxel together with cisplatin as first-line therapy and to see how well it works in treating patients with stage I, stage II, stage III, or stage IV ovarian epithelial cancer.

Detailed Description

OBJECTIVES: * To investigate the efficacy and safety of paclitaxel and cisplatin as first-line chemotherapy in patients with stage IC-IV ovarian epithelial cancer. OUTLINE: This is a multicenter study. Patients receive paclitaxel IV and cisplatin IV once every 2 weeks. Treatment repeats every 2 weeks for 9 courses in the absence of disease progression or unacceptable toxicity.

Registry
clinicaltrials.gov
Start Date
April 2009
End Date
April 2011
Last Updated
12 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Progression-free survival

Secondary Outcomes

  • Overall survival
  • Objective response rate (complete and partial remission in patients with measurable disease)
  • Toxicity

Study Sites (1)

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