The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.
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
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.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
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
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