EUCTR2012-005287-10-ES进行中（未招募）1 期
A Phase III Double-blinded, Placebo Controlled Study of Xilonix? for Improving Survival in Metastatic Colorectal Cancer
XBiotech Germany GmbH0 个研究点目标入组 600 人开始时间: 2015年7月31日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 600
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. Subjects with pathologically confirmed colorectal carcinoma that is metastatic or unresectable and which is refractory to standard therapy. To be considered refractory, a
- •subject must have experienced progression (or intolerance) after treatment with standard
- •approved regimens including, oxaliplatin, irinotecan, flouropyrimidine, bevacizumab, and cetuximab or panitumumab if KRAS wildtype.
- •2. Subjects will not be treated with any radiation, chemotherapy, or investigational agents
- •while enrolled in this protocol.
- •3. Eastern Cooperative Oncology Group (ECOG) performance status 0, 1, or 2.
- •4. At least 2 weeks since the last previous cancer treatment including: chemotherapy,
- •radiation therapy, immunotherapy, surgery, hormonal therapy, or targeted biologics.
- •5. Age ? 18 years, male or female subjects.
- •6. Serum potassium and magnesium levels within institutional normal limits. Total serum calcium or ionized calcium level must be greater than or equal to the lower limit of normal. Subjects with low potassium, calcium and magnesium levels may be replenished to allow for protocol entry.
- •7. Adequate renal function, defined by serum creatinine ?1.5 x ULN.
- •8. Adequate hepatic function defined as:
- •? total bilirubin ?1.5 times the institutional upper limit ULN
- •? alanine aminotransferase (ALT) ? 2.0 times the institutional ULN
- •Exception: subjects with known liver metastases: ? 3.0 times the institutional ULN for ALT.
- •9. Adequate bone marrow function as defined as:
- •? absolute neutrophil count (neutrophil and bands) of ?1,500/mm3 ( ?1.5 x 109/L)
- •? platelet count of ? 100,000/mm3 (?100 x109/L)
- •? hemoglobin of ? 9 g/dL
- •10. For women of childbearing potential (WOCBP), a negative serum pregnancy test result at
- •11. Signed and dated institutional review board (IRB)-approved informed consent before any protocol-specific screening procedures are performed.
- •12. Patients enrolled must, in the Investigator's judgment, be healthy enough to stay on the
- •clinical trial for three months.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 360
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 240
排除标准
- •1. Mechanical obstruction that would prevent adequate oral nutritional intake.
- •2. Serious uncontrolled medical disorder, or active infection, that would impair the ability of
- •the patient to receive protocol therapy.
- •3. Uncontrolled or significant cardiovascular disease, including:
- •? A myocardial infarction within the past 6 months.
- •? Uncontrolled angina within the past 3 months.
- •? Congestive heart failure within the past 3 months, if defined as NYHC-II.
- •? Diagnosed or suspected congenital long QT syndrome.
- •? Any history of clinically significant ventricular arrhythmias (such as ventricular
- •tachycardia, ventricular fibrillation, Wolff-Parkinson-White (WPW) syndrome,
- •or torsade de pointes). Prolonged QTc interval on pre-entry electrocardiogram
- •(>450 msec). If the automated reading is prolonged (i.e., >450 msec), the EKG should be manually over-read.
- •? Any history of second or third degree heart block (may be eligible if currently have a pacemaker).
- •? Heart rate <50 beats per minute on pre-entry electrocardiogram.
- •? Uncontrolled hypertension (blood pressure >140 mm Hg systolic and >90 mm Hg diastolic).
- •4. Dementia or altered mental status that would prohibit the understanding or rendering of
- •informed consent.
- •5. Subjects who have not recovered from the adverse effects of prior therapy at the time of enrollment to ? grade 1; excluding alopecia and grade 2 neuropathy.
- •6. Immunocompromised subjects, including subjects known to be infected with human immunodeficiency virus (HIV).
- •7. Known hepatitis B surface antigen and/or positive hepatitis C antibody and presence of hepatitis C RNA.
- •8. History of tuberculosis (latent or active) or positive Interferon-gamma release assay (IGRA).
- •9. Receipt of a live (attenuated) vaccine within 1 month prior to Screening.
- •10. Subjects with history of hypersensitivity to compounds of similar chemical or biologic composition of Xilonix?.
- •11. Women who are pregnant or breastfeeding.
- •12. WOCBP or men whose sexual partners are WOCBP who are unwilling or unable to use
- •an acceptable method of contraception for at least 1 month prior to study entry, for the duration of the study, and for at least 3 months after the last dose of study medication.
- •13. Weight loss >20% in the previous 6 months.
研究者
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