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临床试验/JPRN-jRCT2080221796
JPRN-jRCT2080221796未知1 期

A Phase 1 Study of veliparib (ABT-888) in Combination with Carboplatin/Paclitaxel in Japanese Subjects with solid tumors

AbbVie GK0 个研究点目标入组 12 人开始时间: 2012年5月23日最近更新:
适应症

试验速览

阶段
1 期
发起方
AbbVie GK
入组人数
12

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • Patients must have histologically or cytologically confirmed malignant solid tumor.
  • - Patients who are amenable to standard combination chemotherapy of carboplatin and paclitaxel.
  • - Patients should have received less than or equal to 1 prior chemotherapy regimens for advanced stage disease.
  • - Eastern Cooperative Oncology Group (ECOG) performance status less than or equal to 2.
  • - Patients must have normal organ and marrow function.

排除标准

  • - Patients who have had chemotherapy or radiotherapy within 3 weeks (6 weeks for nitrosoureas or mitomycin C)
  • prior to entering the study or the adverse events due to agents administered more than 3 weeks earlier have not recovered to less than grade 2.
  • - Known history of allergic reactions to carboplatin or cremophor-paclitaxel.
  • - Patients who have previously received a poly(ADP-ribose) polymerase (PARP) inhibitor.
  • - Uncontrolled intercurrent illness including, but not limited to, ongoing or active systemic infection requiring treatment, symptomatic congestive heart failure, angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
  • - History of seizure disorder.
  • - Hepatitis B surface antigen (HBsAg) positive, Hepatitis C virus (HCV) antibody positive or Human
  • immunodeficiency virus (HIV)-positive patients.

研究者

发起方
AbbVie GK

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