Study of Ramucirumab or Icrucumab (IMC-18F1) With Docetaxel or Docetaxel Alone as Second-Line Therapy in Participants With Bladder,Urethra, Ureter, or Renal Pelvis Carcinoma

Exclusion Criteria

• •Received more than one prior systemic treatment regimen for metastatic disease
• •Received prior systemic taxane therapy (except for prior paclitaxel therapy) for Transitional Cell Carcinoma of the bladder, urethra, ureter, or renal pelvis in any setting (neoadjuvant, adjuvant, metastatic). Prior intravesical taxane therapy is allowed
• •Has received more than one prior anti-angiogenic agent for Transitional Cell Carcinoma of the bladder, urethra, ureter, or renal pelvis
• •Has received radiation therapy within 4 weeks prior to randomization
• •Has a history of uncontrolled hereditary or acquired bleeding or thrombotic disorders
• •Has experienced a Grade ≥ 3 bleeding event (eg, via gastric ulcers, gastric varices, or gross hematuria) within 3 months prior to randomization
• •Has uncontrolled intercurrent illness including, but not limited to symptomatic anemia, uncontrolled hypertension, symptomatic congestive heart failure, unstable angina pectoris, symptomatic or poorly controlled cardiac arrhythmia, psychiatric illness/social situations, or any other serious uncontrolled medical disorders
• •Has experienced any arterial thrombotic or thromboembolic events, including but not limited to myocardial infarction, transient ischemic attack or cerebrovascular accident, within 6 months prior to randomization
• •Has known brain metastases, uncontrolled spinal cord compression, or leptomeningeal disease
• •Has an ongoing or active infection requiring parenteral antibiotic, antifungal, or antiviral therapy
• •Has known human immunodeficiency virus infection or acquired immunodeficiency syndrome
• •Has received a prior autologous or allogeneic organ or tissue transplantation
• •Received chemotherapy within 21 days prior to randomization; and/or is currently enrolled in, or discontinued within 21 days prior to randomization from, a clinical trial involving an investigational product or unapproved use of a drug or device (other than the study drug\[s\] used in this study), or is concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study; and/or was treated with anti-angiogenic therapy within 28 days prior to randomization
• •Has undergone major surgery within 28 days prior to randomization, or subcutaneous venous access device placement within 7 days prior to randomization
• •Has had a serious nonhealing wound, ulcer, or bone fracture within 28 days prior to randomization
• •Has an elective or planned major surgery to be performed during the course of the trial
• •Is pregnant or lactating
• •Has a concurrent active malignancy other than adequately treated non-melanomatous skin cancer, curatively treated cervical carcinoma in-situ, other noninvasive carcinoma or in-situ neoplasm, or prostate cancer with an undetectable prostate specific antigen (PSA) and no current treatment with hormone therapy
• •Has an acute/subacute bowel obstruction or history of chronic diarrhea requiring ongoing medical intervention
• •History of gastrointestinal perforation and/or fistula within 6 months prior to randomization
• •Has active diverticulitis
• •Known hypersensitivity to docetaxel or other drugs formulated with polysorbate 80
• •Known hypersensitivity to agents of similar biologic composition as ramucirumab DP, IMC-18F1, or other agents that specifically target vascular endothelial growth factor receptor (VEGF)