Study:
A Dose Escalating Phase I Study With An Expanded Cohort To Assess The Feasibility Of Intraperitoneal Carboplatin (NSC #214240) And Intravenous Paclitaxel (NSC # 673089) In Patients With Previously Untreated Epithelial Ovarian, Primary Peritoneal, Or Fallopian Tube Carcinoma
Rationale:
Drugs used in chemotherapy, such as carboplatin and paclitaxel, work in different
ways to stop tumor cells from dividing so they stop growing or die. Combining more than one
chemotherapy drug may kill more tumor cells.
Purpose:
This phase I trial is studying the side effects and best dose of adjuvant
intraperitoneal carboplatin when given together with paclitaxel in treating patients who have
undergone debulking surgery for stage II, stage III, or stage IV ovarian epithelial, primary
peritoneal, or fallopian tube cancer.
Study Status: Recruiting
Recruiting:
Clinical Trials Office - Cleveland Clinic Taussig Cancer Cente 866-223-8100
| Condition |
Intervention |
Phase |
Fallopian Tube Cancer Ovarian Cancer Peritoneal Cavity Cancer |
Drug: carboplatin Drug: paclitaxel Procedure: adjuvant therapy |
Phase 1 |
Verified by
Gynecologic Oncology Group
February, 2009
Sponsored by: Gynecologic Oncology Group
Information provided by: National Cancer Institute (NCI)
ClinicalTrials.gov identifier: NCT00079430
Study Type: Interventional
Study Design: Treatment
Cleveland Clinic Taussig Cancer Center
Cleveland, Ohio 44195
United States
Mark A. Morgan, MD, FACOG, FACS., Study Chair