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临床试验/JPRN-UMIN000045131
JPRN-UMIN000045131招募中未知

Comprehensive analysis of cytokines and PD-L1 before and after administration of Atezolizumab and Bevasizumab in patients with HCC - ASTRAL-HCC

ational Center for Global Health and Medicine0 个研究点目标入组 20 人开始时间: 2021年9月1日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1) Current use of anticoagulants or antiplatelets or prior use within 10 days (2) High risk of bleeding or untreated/incompletely treated esophageal/gastric varix (3) Thrombosis or embolism within 180 days (4) Major surgery within 28 days (5) Use of immunostimulants within 180 days (6) Use of immunosuppressants within 14 days (7) Autoimmune disease within 180 days (8) Double cancer or prior malignant neoplasm except early malignancy (9) Enrollment to an intervention study or a study using unapproved drug (10) Severe cardiovascular disease, unstable arrhythmia, unstable angina within 90 days (11) Pregnancy, breastfeeding, no approve for contraception (12) Uncontrollable pleural effusion, pericardial fluid, or ascites (13) Hepatic encephalopathy (14) Uncontrollable hypertension, severe infection, hemodialysis (15) Allergy or anaphylactic reaction to chimeric antibody, humanized antibody, or fusion protein (16) Allergy to atezolizumab and bevasizumab (17) Current or prior active hemorrhagic disease (18) Oral feeding difficulty (19) HIV positivity (20) Active pulmonary fibrosis or interstitial pneumonia (21) Blood transfusion or G-CSF within 14 days (22) Unsuitable patient at a physician's decision

研究者

发起方
ational Center for Global Health and Medicine

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