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Phase 2 Randomized, Multicenter Study of IMC-A12 as a Single Agent or in Combination With Antiestrogens in Postmenopausal Women With Hormone Receptor-Positive Advanced or Metastatic Breast Cancer After Progression on Antiestrogen Therapy
The purpose of this study is to determine whether IMC-A12 offers increased progression-free survival (PFS) associated with IMC-A12 monotherapy and IMC-A12 in combination with an antiestrogen therapy in patients with hormone receptor positive advanced or metastatic breast cancer that have experienced disease progression on antiestrogen therapy.
Breast cancer is the most common form of malignancy affecting women worldwide, with approximately 178,480 new cases of invasive breast cancer and 62,030 new cases of in situ breast cancer expected in the United States (US) in 2007. Approximately 40,460 women are expected to die of breast cancer in the coming year, making the disease the second leading cause of cancer-related mortality among women (trailing only cancers of the lung and bronchus). However, thanks in part to recent advances in treatment, mortality rates associated with breast cancer have declined consistently since 1990. Surgical resection and other treatments may particularly benefit patients whose disease is identified prior to metastasis; the 5-year survival rate for patients diagnosed with locoregionally advanced disease is 83%. However, women with distant metastases at diagnosis have a much poorer outlook, with a 5-year survival rate of only 26% and a median survival of approximately 2 years. Treatment of advanced disease may include first-line chemotherapy utilizing an anthracycline (eg, doxorubicin or epirubicin), antibody therapy, limited surgery, taxanes, and other cytotoxic agents. As complete responses are rare, these treatments are not generally employed as curative but in an effort to prolong life and provide symptom palliation. Approximately two-thirds of all breast cancers are positive for expression of the estrogen receptor.For patients whose tumors are positive for this receptor or the progesterone receptor, the preferred first-line treatment comprises blockade of estradiol synthesis or hormone receptor activity using aromatase inhibitors or antiestrogen agents. Although endocrine therapies are useful and well-tolerated, most patients respond to this form of treatment for about 12-18 months before developing refractory disease. New therapies able to provide additional benefit to patients with hormone receptor-positive, antiestrogen-refractory, advanced and metastatic breast cancer are required.
Age
18 - No limit years
Sex
FEMALE
Healthy Volunteers
No
ImClone Investigational Site
Scottsdale, Arizona, United States
ImClone Investigational Site
Chicago, Illinois, United States
ImClone Investigational Site
Westwood, Kansas, United States
ImClone Investigational Site
Rochester, Minnesota, United States
ImClone Investigational Site
Lebanon, New Hampshire, United States
ImClone Investigational Site
New York, New York, United States
ImClone Investigational Site
The Bronx, New York, United States
ImClone Investigational Site
Columbus, Ohio, United States
ImClone Investigational Site
Nashville, Tennessee, United States
Start Date
August 1, 2008
Primary Completion Date
March 1, 2012
Completion Date
February 1, 2015
Last Updated
June 6, 2018
93
ACTUAL participants
IMC-A12 (cixutumumab)
BIOLOGICAL
tamoxifen
DRUG
Anastrozole
DRUG
Letrozole
DRUG
Exemestane
DRUG
Fulvestrant
DRUG
Lead Sponsor
Eli Lilly and Company
NCT06625775
NCT06649331
Data Source & Attribution
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