EUCTR2007-004645-15-NL进行中（未招募）不适用
Phase 1B Study of the Safety, Tolerance, and Pharmacokinetics of Oral Posaconazole in Immunocompromised Children With Neutropenia
Schering Plough Research Institute, A Division of Schering Corporation0 个研究点目标入组 108 人开始时间: 2010年5月25日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 108
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. Children of either sex and of any race, 3 months to <18 years of age.
- •2. Subjects must have documented or anticipated neutropenia (ANC < or equal to 500/mm3 [0.5 x 10^9/L]) expected to last for at least 7 days and only in the following clinical situations: Acute leukemia (including new and relapse), Myelodysplasia, Severe aplastic anemia, Autologous HSCT recipients, High risk neuroblastoma, Advanced stage non-Hodgkin’s lymphoma.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Subjects with proven IFI, as defined by the MSG/EORTC criteria prior to study entry
- •2. Subjects with Grade 3 or Grade 4 nausea and/or vomiting at Screening
- •3. Subjects who have received POS within the past 10 days prior to Screening
- •4. Subjects receiving prohibited drugs (please refer to Table 3)
- •5. Subjects whose laboratory tests are outside normal limits as follows:
- •a. AST or ALT > 5 times the upper limit of normal (ULN)
- •b. Serum total bilirubin >2.5 x ULN
- •c. Calculated creatinine clearance <30 mL/min. Creatinine clearance will be calculated using the following equation: Calculated Creatinine clearance = k*height(cm)/serum creatinine (mg/dL) Where k=0.45 for a full term baby less than 1 year old; 0.55 for children up to 12 years old; 0.55 for females between the ages of 13 and 21 years; 0.7 for males between the ages of 13 and 21 years
- •6. Subjects with QTc prolongation:
- •a. Symptomatic QTc prolongation >450msec (males) or >470msec (females)
- •b. Any QTc prolongation of >500msec
- •7. Subjects who are unable to receive drug enterally
- •8. Females subjects who are pregnant, intend to become pregnant during the course of this study, or are breast feeding
- •9. Subjects with a history of anaphylaxis attributed to the azole class of antifungal agents.
- •10. Subjects with any clinically significant condition or situation, other than the condition being studied that, in the opinion of the investigator, would interfere with the study evaluations or optimal participation in the study, including receiving less than 7 days of POS
- •11. Subjects who have already participated in this study or are participating in any Phase 1 clinical study or any study for a medication that has not yet received regulatory approval
- •12. Subjects who are part of the study staff personnel or family members of the study staff personnel.
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