Status:
COMPLETED
A Study of Ramucirumab (IMC-1121B) in Participants With Breast Cancer
Lead Sponsor:
Eli Lilly and Company
Conditions:
Breast Cancer
Metastatic Breast Cancer
Eligibility:
FEMALE
20+ years
Phase:
PHASE1
Brief Summary
The primary objective of this study is to investigate the safety and tolerability of the anti-VEGFR-2 monoclonal antibody ramucirumab drug product in combination with docetaxel in Japanese participant...
Eligibility Criteria
Inclusion
- The participant is Japanese
- The participant has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- The participant has a histopathologically or cytologically confirmed diagnosis of breast adenocarcinoma that is now metastatic or locally-recurrent and inoperable with curative intent
- The participant has measurable and/or non-measurable disease
- The participants' primary and/or metastatic tumor is Human Epidermal Growth Factor Receptor 2 (HER2) negative
- The participant received neo adjuvant or adjuvant taxane therapy ≥ 6 months prior to the study
- The participant received neo adjuvant or adjuvant biologic therapy ≥ 6 weeks prior to the study
- The participant completed all prior radiotherapy ≥ 3 weeks prior to the study registration date
- The participant received prior hormonal therapy for breast cancer in the neo adjuvant, adjuvant,and/or the metastatic setting ≥ 2 weeks prior to the study registration date
- The participant's left ventricular ejection fraction (LVEF) is within normal ranges
- The participant has adequate hematologic, hepatic, and coagulation function.
- Eligible participants of reproductive potential agree to use adequate contraceptive methods (hormonal or barrier methods) during the study period and for 12 weeks after the last dose of study medication
Exclusion
- The participant has a concurrent active malignancy other than breast adenocarcinoma, adequately treated non-melanomatous skin cancer, or other non-invasive carcinoma or in situ neoplasm. Participants with previous treatment of malignancy is eligible, provided that she has been disease free for \>3 years
- The participant has a known sensitivity to docetaxel
- The participant has a known sensitivity to agents of similar biologic composition as ramucirumab
- The participant has a history of chronic diarrheal disease within 6 months prior to the study registration date
- The participant has received irradiation to a major bone marrow area within 30 days prior to the study registration date
- The participant has received any experimental agents within 4 weeks prior to the study registration date
- The participant has a history of uncontrolled hereditary or acquired bleeding or thrombotic disorders
- The participant has Grade 3-4 bleeding within 3 months prior to the study registration date
- The participant has an ongoing or active infection requiring antibiotic, antifungal, or antiviral therapy
- The participant has uncontrolled hypertension, symptomatic congestive heart failure, psychiatric illness, or any other serious uncontrolled medical disorders
- The participant has brain metastases
- The participant has known human immunodeficiency virus infection or acquired immunodeficiency syndrome related illness
- The participant is pregnant or lactating
- The participant has not fully recovered from effects of prior chemotherapy
- The participant has undergone major surgery within 28 days prior to the study registration date
Key Trial Info
Start Date :
December 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2013
Estimated Enrollment :
7 Patients enrolled
Trial Details
Trial ID
NCT01256567
Start Date
December 1 2010
End Date
February 1 2013
Last Update
June 18 2014
Active Locations (4)
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1
ImClone Investigational Site
Hidaka, Japan, 350-1298
2
ImClone Investigational Site
Matsuyama, Japan, 790-0007
3
Imclone Investigational Site
Nagoya, Japan, 464-8681
4
ImClone Investigational Site
Osaka, Japan, 540-0006