Dosing schedule for participants.

Figshare2015-12-03 更新2026-04-29 收录

疫苗临床试验

接种时间安排

数据链接：

https://figshare.com/articles/dataset/_Dosing_schedule_for_participants_/1333872 数据链接链接失效反馈

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资源简介：

Dose 1 of vaccine was given on day 0 in both groups, whereas dose 2 was given either on day 14 or day 28Dosing schedule for participants.

创建时间：

2015-12-03

ATN 025 Concomitant Medications [CRF 4] Dataset in Hepatitis B Vaccination in Youth at Adolescent Trials Network Sites: Effectiveness of Two Strategies and Evaluation of Tools to be Used in Future HIV Prevention Trials

疫苗临床试验

HIV青少年健康

Data from Concomitant Medications [CRF 4] Study Description A randomized, single-blinded trial evaluating two licensed vaccine products, Recombivax and Twinrix, given in a two-dose schedule to youth a

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First-in-human randomized controlled trial of an oral, replicating adenovirus 26 vector vaccine for HIV-1

疫苗临床试验

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BackgroundLive, attenuated viral vectors that express HIV-1 antigens are being investigated as an approach to generating durable immune responses against HIV-1 in humans. We recently developed a repli

Figshare2018-11-14 更新40

Characteristics of HVTN 502 and 503 trial participants.

疫苗临床试验

免疫基因型分析

Data shown are median values (interquartile range) unless otherwise indicated. * At time of sampling § HLA-B*27, B51, B*5701/03, B*5801 and B*8101 Characteristics of HVTN 502 and 503 trial participant

NIAID Data Ecosystem20

Safety and immunogenicity of an inactivated whole cell tuberculosis vaccine booster in adults primed with BCG: A randomized, controlled trial of DAR-901

疫苗临床试验

结核病免疫

Background Development of a tuberculosis vaccine to boost BCG is a major international health priority. SRL172, an inactivated whole cell booster derived from a non-tuberculous mycobacterium, is the o

NIAID Data Ecosystem40

ATN 076 Monitoring Untoward Effects Form [CRF 96] Dataset in Evaluation of an Intervention to Reduce Preventive Misconception in HIV Vaccine Clinical Trials

疫苗临床试验

知情同意干预

Dataset with no observations Study Description A randomized, preliminary proof of concept study evaluating two types of supplemental information that would serve as an adjunct to the traditional infor

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Dosing schedule for participants.

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