Breast Cancer Clinical Trial

Enzastaurin For Breast Cancer Patients Who Previously Received an Anthracycline and a Taxane Chemotherapy

Summary

The purpose of this study is to determine the effectiveness of enzastaurin in the treatment of patients with metastatic breast cancer.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Clinical diagnosis of metastatic breast cancer or recurrent breast cancer where surgery can not be done for curative intent
Have received prior therapy with an anthracycline (class of drugs) and a taxane (class of drugs).
Tumors must not be positive for HER2, but if positive, the treatment plan should not include further treatment with the drug Herceptin.
Disease that can be definitely measured on Cat Scans or other radiological tests.
May have received high dose chemotherapy for autologous stem cell support greater than or equal to 6 months of starting this study.

Exclusion Criteria:

More than 2 chemotherapy regimens for metastatic or locally recurrent disease.
Have brain cancer from breast cancer
Pregnant or breastfeeding
Have an inability to swallow tablets
Within 6 months have had a serious heart condition

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

41

Study ID:

NCT00386087

Recruitment Status:

Completed

Sponsor:

Eli Lilly and Company

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There are 4 Locations for this study

See Locations Near You

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Newark Delaware, 19713, United States
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Indianapolis Indiana, 46202, United States
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
South Bend Indiana, 46601, United States
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Boston Massachusetts, 02115, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

41

Study ID:

NCT00386087

Recruitment Status:

Completed

Sponsor:


Eli Lilly and Company

How clear is this clinincal trial information?

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