Immune Response to Influenza Vaccine in Subjects with B-cell Malignancies Treated with Idelalisib

Gilead Sciences, Inc.0 个研究点目标入组 22 人开始时间: 2018年5月15日最近更新: 2019年12月10日

试验速览

阶段: 1 期
状态: 进行中（未招募）
发起方: Gilead Sciences, Inc.
入组人数: 22

研究概览入排标准研究者记录与标识符相似试验

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

入选标准

•1) = 18 years of age;
•2) Currently enrolled in a Gilead-sponsored study, receiving or scheduled to initiate treatment with idelalisib for at least 7 consecutive days prior to receiving an influenza vaccine;
•3) Will be receiving an influenza vaccine per standard of care;
•4) Willing to comply with scheduled visits, laboratory tests, other study procedures, and study restrictions;
•5) Signed informed consent form, indicating that the subject has been informed of the procedures to be followed, potential risks and discomforts, and other pertinent aspects of study participation.
•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 11
•F.1.3 Elderly (>=65 years) yes
•F.1.3.1 Number of subjects for this age range 11

排除标准

•1) Administration of systemic steroids for more than 2 consecutive weeks within the past 3 months (i.e., 12 weeks) prior to receiving an influenza vaccination. Up to 3 single doses of systemic corticosteroids (e.g., given as a premedication) are permitted within 30 days prior to receiving an influenza vaccine, however none of these doses may be administered within 7 days prior to vaccination. Topical and inhaled steroids are permitted.
•2) Intravenous immunoglobulin (IVIG) therapy within the past 3 months (i.e., 12 weeks) prior to receiving an influenza vaccination, and/or planned administration during the study period.
•3) Cytotoxic chemotherapy and chronic administration (more than 14 days) of immunosuppressants within 30 days of vaccination.
•4) Vaccination against influenza within the last 24 weeks prior to vaccination in this study, and/or planned administration of a second dose of influenza vaccine during the study period.
•5) Receipt of any vaccine in the 4 weeks preceding the trial vaccination or planned receipt of any vaccine in the 4 weeks following trial vaccination.
•6) History of severe allergic or hypersensitivity reaction that is likely to be exacerbated by any component of an influenza vaccine including egg and chicken protein, or history of hypersensitivity to a previous dose of an influenza vaccine.
•7) Acute disease and/or fever at the time of baseline blood draw (fever is defined as temperature
•= 38°C in an oral setting).
•8) Presence of any condition that could, in the opinion of the investigator, compromise the subject’s ability to participate in the study, such as history of substance abuse or psychiatric condition.
•9) Females who are pregnant or lactating (refer to the Gilead-sponsored parent study’s definition of ‘child-bearing potential’ to determine if pregnancy testing is required. If a pregnancy test has been performed in the Gilead-sponsored parent study = 6 weeks prior to the baseline blood draw, it may be used for eligibility purposes. If a pregnancy test has not been performed in > 6 weeks, a urine pregnancy test should be performed locally).

研究者

发起方

Gilead Sciences, Inc.

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