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Spots Global Cancer Trial Database for A Phase 1-2, XIAP Antisense AEG35156 With Weekly Paclitaxel in Patients With Advanced Breast Cancer

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Trial Identification

Brief Title: A Phase 1-2, XIAP Antisense AEG35156 With Weekly Paclitaxel in Patients With Advanced Breast Cancer

Official Title: A Phase 1-2, Multicenter, Open-Label Study of the X-Linked Inhibitor of Apoptosis (XIAP) Antisense AEG35156 Given in Combination With Weekly Paclitaxel in Patients With Advanced Breast Cancer

Study ID: NCT00558545

Interventions

AEG35156

Study Description

Brief Summary: This is an open-label multicenter, phase 1-2 study. Following determination of the recommended AEG35156 dose in combination with weekly paclitaxel in the initial Phase 1 part of this study, additional patients will be enrolled in the Phase 2 part of the study to assess the activity of the combination in advanced breast cancer.

Detailed Description: Breast cancer is the most common cancer in women in the United States, the second most common cause of cancer death, and the main cause of death in women ages 45 to 55. In 2006, 212,920 American women will be diagnosed with breast cancer, and 40,970 will die from this disease.\[1\]. Fewer than 10 percent of women present with metastatic disease at the time of diagnosis. However, the majority of women who relapse after initial definitive therapy for early stage or locally advanced disease will do so with disseminated metastatic disease rather than an isolated local recurrence. Treatment for metastatic disease is palliative in intent and will usually involve hormone therapy and/or chemotherapy with or without trastuzumab. Active chemotherapy agents include anthracyclines, taxanes, vinorelbine, alkylating agents and antimetabolites. Taxanes have become the cornerstone of first-line treatment for metastatic breast cancer. Weekly doses of paclitaxel can be administered continuously for several weeks with a remarkable lack of myelosuppression \[2\]. Weekly paclitaxel (80 mg/m2) was directly compared to every three-week therapy (175 mg/m2) in 585 women with metastatic breast cancer. Weekly therapy was associated with a significantly higher response rate (40 versus 28 percent) and longer TTP (nine versus five months), but similar overall survival and worse neurotoxicity \[3\]. Since patients with metastatic breast cancer are unlikely to be cured of their disease \[4\], they should be considered candidates for a clinical trial.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Rocky Mountain Cancer Center, Denver, Colorado, United States

Cancer Centers of Florida, P.A., Ocoee, Florida, United States

Central Indiana Cancer Center, Indianapolis, Indiana, United States

New York Oncology & Hematology P. C., Albany Cancer Center, Albany, New York, United States

Dayton Oncology & Hematology, P.A., Dayton, Ohio, United States

Cancer Centers of the Carolinas, Greenville, South Carolina, United States

Sammons Cancer Center, Dallas, Texas, United States

Tyler Cancer Center, Tyler, Texas, United States

Virginia Oncology Associates, Norfolk, Virginia, United States

Northwest Cancer Specialists, P. C., Vancouver, Washington, United States

Contact Details

Name: David M Loesch, MD

Affiliation: Central Indiana Cancer Centers

Role: PRINCIPAL_INVESTIGATOR

Name: Jacques Jolivet, MD, FACP

Affiliation: Aegera Therapeutics, Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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