E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
HER2-Negative, Unresectable, Locally-Recurrent or Metastatic Breast Cancer |
|
MedDRA Classification |
E.1.2 Medical condition or disease under investigation |
E.1.2 | Version | 9.1 |
E.1.2 | Level | LLT |
E.1.2 | Classification code | 10027475 |
E.1.2 | Term | Metastatic breast cancer |
|
E.1.3 | Condition being studied is a rare disease | No |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
The primary objective of this study is to compare the PFS of the drug combination IMC -1121B plus docetaxel to placebo plus docetaxel in previously untreated patients with HER2-negative, unresectable, locally-recurrent or metastatic breast cancer. |
|
E.2.2 | Secondary objectives of the trial |
The secondary objectives of this study are: · to compare the overall survival of the drug combination IMC -1121B plus docetaxel to placebo plus docetaxel in previously untreated patients with HER2-negative, unresectable, locally-recurrent or metastatic breast cancer · to compare the TTP, ORR, and duration of response between the two treatment arms · to compare the safety of the two treatment arms · to compare the quality of life of the two treatment arms · to assess the immunogenicity of IMC-1121B |
|
E.2.3 | Trial contains a sub-study | No |
E.3 | Principal inclusion criteria |
Each patient must meet the following criteria to be randomized in this study: 1. The patient is able to provide signed informed consent. 2. The patient is female and ≥ 18 years of age or older if required by local laws or regulations. 3. The patient has histologically or cytologically confirmed adenocarcinoma of the breast that is now metastatic or locally-recurrent and inoperable with curative intent. Every effort should be made to make paraffin-embedded tissue or slides from the diagnostic biopsy or surgical specimen available for confirmation of diagnosis. 4. The patient has measurable and/or non-measurable disease. 5. The patients’ primary and/or metastatic tumor is HER2-negative by fluorescence in situ hybridization (FISH) or chromogenic in-situ hybridization (CISH) or 0, 1+ overexpression by immunohistochemistry (IHC). 6. The patient has not received prior chemotherapy for metastatic or locally recurrent and inoperable breast cancer. 7. The patient completed (neo) adjuvant taxane therapy at least 6 months prior to randomization. 8. The patient completed (neo) adjuvant biologic therapy at least 6 weeks prior to randomization. 9. The patient completed all prior radiotherapy with curative intent ≥ 3 weeks prior to randomization. 10. The patient may have received prior hormonal therapy for breast cancer in the (neo) adjuvant and/or the metastatic setting ≥ 2 weeks prior to randomization. 11. The patient’s left ventricular ejection fraction is within normal institutional ranges. 12. The patient has resolution to grade ≤ 1 by the National Cancer Institute Common Terminology Criteria for Adverse Events, Version 3 (NCI-CTCAE v 3.0) of all clinically significant toxic effects of prior chemotherapy, surgery, radiotherapy, or hormonal therapy with the exception of peripheral neuropathy which must have resolved to grade ≤ 2. 13. The patient has an Eastern Cooperative Oncology Group (ECOG) performance status of 0-1. 14. The patient is amenable to compliance with protocol schedules and testing. 15. The patient has adequate hematological functions (absolute neutrophil count [ANC] ≥ 1500 cells/mL, hemoglobin ≥ 9 g/dL, and platelets ≥ 100,000 cells/mL and ≤ 850,000 cells/mL). 16. The patient has adequate hepatic function (bilirubin within normal limits [WNL], aspartate transaminase [AST] and alanine transaminase [ALT] ≤ 2.5 times the upper limit of normal [ULN], or ≤ 5.0 times the ULN if the transaminase elevation is due to liver metastases, and alkaline phosphatase ≤ 5.0 times the ULN). 17. The patient has serum creatinine ≤ 1.5 x ULN. If serum creatinine > 1.5 x ULN the calculated creatinine clearance should be > 40 mL/min). 18. The patient’s urinary protein is ≤ 1+ on dipstick or routine urinalysis (UA); if urine protein ≥ 2+, a 24-hour urine collection must demonstrate < 1000 mg of protein in 24 hours to allow participation in the study. 19. The patient must have adequate coagulation function as defined by international normalized ratio (INR) ≤ 1.5 and a partial thromboplastin time (PTT) ≤ 1.5 X ULN if not receiving anticoagulation therapy. Patients on full-dose anticoagulation must be on a stable dose of oral anticoagulant or low molecular weight heparin and if on warfarin must have a INR between 2 and 3 and have no active bleeding (defined as within 14 days of randomization) or pathological condition that carries a high risk of bleeding (eg, tumor involving major vessels or known varices). 20. Women of childbearing potential must implement adequate contraception in the opinion of the investigator. |
|
E.4 | Principal exclusion criteria |
A patient who has any of the following criteria will be excluded from the study: 1. The patient has a concurrent active malignancy other than breast adenocarcinoma, adequately treated non-melanomatous skin cancer, or other non-invasive carcinoma or in situ neoplasm. A patient with previous history of malignancy is eligible, provided that she has been disease free for > 3 years. 2. The patient has a known sensitivity to docetaxel or other drugs formulated with polysorbate 80. 3. The patient has a known sensitivity to agents of similar biologic composition as IMC-1121B or other agents that specifically target VEGF. 4. The patient has a history of chronic diarrheal disease within 6 months prior to randomization. 5. The patient has received irradiation to a major bone marrow area as defined as > 25% of bone marrow (eg, pelvic or abdominal radiation) within 30 days prior to randomization. 6. The patient has participated in clinical trials of experimental agents within 4 weeks prior to randomization. 7. The patient has a history of uncontrolled hereditary or acquired bleeding or thrombotic disorders. 8. The patient has active, high risk bleeding (eg, via gastric ulcers or gastric varices) within 14 days prior to randomization. 9. The patient has an ongoing or active infection requiring parenteral antibiotic, antifungal, or antiviral therapy. 10. The patient has 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 in the opinion of the investigator. 11. The patient has brain metastases, uncontrolled spinal cord compression, or carcinomatous meningitis, or new evidence of brain or leptomeningeal disease. 12. The patient has known human immunodeficiency virus infection or acquired immunodeficiency syndrome-related illness. 13. The patient has pulmonary lymphangitic involvement that results in pulmonary dysfunction requiring active treatment, including the use of oxygen. 14. The patient is pregnant or lactating. |
|
E.5 End points |
E.5.1 | Primary end point(s) |
The primary efficacy endpoint of this trial, Progression Free Survival, is defined as the time from randomization until the first evidence of progression as defined by RECIST, modified based on current practice of the medical community, or death from any cause. Patients who did not progress will be censored at the day of their last radiographic tumor assessment, if available, or date of randomization if no post initiation radiographic assessment is available. Patients who do not receive study treatment and who have neither progressed nor died will be censored at the day of their last radiographic tumor assessment, if available, or date of randomization if no post initiation radiographic assessment is available. If there are no postbaseline tumor measurements for randomized and treated patients, the patient will be censored at the date of randomization. If death or PD occurs after two or more missing radiographic visits, censoring will occur at the date of the last radiographic visit. The final analysis of PFS will include sensitivity analyses under the following conditions: · using the investigator PFS results - as provided, including symptomatic/clinical deterioration as a progression outcome - censoring symptomatic/clinical deterioration as a progression outcome to parallel the IRC results using only objective response · using the IRC provided PFS from the Per Protocol population · using the IRC provided PFS results from the ITT population, considering different censoring rules to control for missing data and/or lost to follow-up, as described in the Statistical Analysis Plan (SAP). |
|
E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | No |
E.6.2 | Prophylaxis | No |
E.6.3 | Therapy | Yes |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | No |
E.6.7 | Pharmacodynamic | No |
E.6.8 | Bioequivalence | No |
E.6.9 | Dose response | No |
E.6.10 | Pharmacogenetic | Yes |
E.6.11 | Pharmacogenomic | No |
E.6.12 | Pharmacoeconomic | No |
E.6.13 | Others | Yes |
E.6.13.1 | Other scope of the trial description |
immunogenicity and circulating tumor cells testing |
|
E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | No |
E.7.1.1 | First administration to humans | No |
E.7.1.2 | Bioequivalence study | No |
E.7.1.3 | Other | No |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | No |
E.7.3 | Therapeutic confirmatory (Phase III) | Yes |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | Yes |
E.8.1.1 | Randomised | Yes |
E.8.1.2 | Open | No |
E.8.1.3 | Single blind | No |
E.8.1.4 | Double blind | Yes |
E.8.1.5 | Parallel group | Yes |
E.8.1.6 | Cross over | No |
E.8.1.7 | Other | No |
E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | No |
E.8.2.2 | Placebo | Yes |
E.8.2.3 | Other | No |
E.8.3 |
The trial involves single site in the Member State concerned
| No |
E.8.4 | The trial involves multiple sites in the Member State concerned | Yes |
E.8.4.1 | Number of sites anticipated in Member State concerned | 5 |
E.8.5 | The trial involves multiple Member States | Yes |
E.8.5.1 | Number of sites anticipated in the EEA | 64 |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | Yes |
E.8.6.2 | Trial being conducted completely outside of the EEA | Information not present in EudraCT |
E.8.6.3 | If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned |
|
E.8.7 | Trial has a data monitoring committee | Yes |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
| |
E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | 7 |
E.8.9.1 | In the Member State concerned months | |
E.8.9.1 | In the Member State concerned days | |
E.8.9.2 | In all countries concerned by the trial years | 7 |