This trial is active, not recruiting.

Condition endometrial cancer
Treatment e7080
Phase phase 2
Target VEGF
Sponsor Eisai Inc.
Start date February 2010
End date May 2012
Trial size 167 participants
Trial identifier NCT01111461, E7080-G000-204


The purpose of this study is to assess the objective response rate of E7080 in subjects with advanced endometrial cancer and disease progression following platinum-based, first line chemotherapy.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation non-randomized
Endpoint classification safety/efficacy study
Intervention model single group assignment
Masking open label
Primary purpose treatment
E7080 capsules are administered orally once a day in 28 day cycles to patients with advanced endometrial cancer and disease progression following first-line chemotherapy.

Primary Outcomes

Objective response rate
time frame: 24 weeks

Eligibility Criteria

Female participants at least 18 years old.

Inclusion criteria: Histologically confirmed diagnosis of endometrial carcinoma Radiographic evidence of disease progression according to modified RECIST 1.1 after 1 prior systemic, platinum-based chemotherapy regimen for recurrent metastatic or primary unresectable endometrial carcinoma for which no surgical or radiotherapy treatment option exists Measureable disease meeting the following criteria: - At least 1 lesion of greater than 1.5 cm in the longest diameter for a non-lymph node or greater than 1.5 cm in the short-axis diameter for a lymph node which is is serially measureable according to modified RECIST 1.1 using computerized tomography / magnetic resonance imaging - Lesions that have had external beam radiotherapy (EBRT) or loco-regional therapies such as radiofrequency ablation must show evidence of progressive disease based on modified RECIST 1.1 to be deemed a target lesion. Eastern Cooperative Oncology Group (ECOG) performance status less than 2. Adequately controlled blood pressure with or without antihypertensive medications, defined as BP less than 150/90 mmHg at screening and no change in antihypertensive medications within 1 week prior to the Screening Visit Adequately renal function defined as calculated creatinine clearance greater than 30 mL/min per the Cockcroft and Gault formula Adequate bone marrow function: - Absolute neutrophil count greater than1000/mm3 (greater than 1.0 x 103/u/L); - Platelets greater than100,000/mm3 (greater than100 x 109/L); - Hemoglobin greater than 9.0 g/dL Adequate blood coagulation function as evidenced by an International Normalized Ratio less than 1.5 Adequate liver function: - Bilirubin less than 1.5 x ULN except for unconjugated hyperbilirubinaemia of Gilbert's syndrome - Alkaline Phosphatase, alanine aminotransferase and aspartate aminotransferase less than 3 X ULN (greater than 5 x ULN if subject has liver metastasis) Age greater than 18 years at time of informed consent Must have negative serum or urine pregnancy test for women of reproductive potential Exclusion criteria: Brain or leptomeningeal metastases, including stable metastases More than 1 prior systemic chemotherapy regimen for recurrent metastatic or primary unresectable endometrial carcinoma or any treatment targeting vascular endothelial growth factor (VEGF)-directed angiogenesis. No restriction regarding prior adjuvant chemotherapy or hormonal therapy Prior systemic anti-tumor therapy within 3 weeks Not fully recovered from prior radiotherapy based on investigator judgement Subjects with greater than 1+ proteinuria on urine dipstick testing will undergo 24-hour urine collection for quantitative assessment of proteinuria. Subjects with greater than 1 gm will be ineligible Gastrointestinal malabsorption or any other condition that might affect teh absorption of E7080 Inability to take oral medication Major surgery within 3 weeks prior to first dose of study drug Significant cardiovascular impairment: hx of congestive heart failure greater than New York Heart Association Class II; unstable angina; myocardial infarction or stroke within 6 months of the first dose of study drug; cardiac arrhythmia requiring medical treatment Prolongation of QTc interval greater than 480 msec. Bleeding disorder or thrombotic disorders requiring anticoagulant therapy, such as warfarin, or similar agents requiring therapeutic INR monitoring (treatment with low molecular weight heparin [LMWH] allowed). Active hemoptysis within 3 weeks prior to the first dose of study drug Known intolerance to the study drug ( or any of the excipients) Any medical or other conditions which, in the opinion of the investigator, would preclude participation in a clinical trial Active malignancy in the past 2 years other than endometrial cancer unless histologic proof is available demonstrating that recurrent disease is a relapse of endometrial carcinoma Previous treatment with an investigational drug within 30 days prior to first dose of study drug Females who are pregnant or breast feeding.

Additional Information

Official title An Open-Label, Single-Arm, Multicenter Phase II Study of E7080 in Subjects With Advanced Endometrial Cancer and Disease Progression Following First-Line Chemotherapy
Trial information was received from ClinicalTrials.gov and was last updated in January 2015.
Information provided to ClinicalTrials.gov by Eisai Inc..