摘要
肿瘤已经逐渐发展成为老年伴侣动物最为常见的疾病,而目前国内并无伴侣动物专用的抗肿瘤药。细胞毒类抗肿瘤药是治疗恶性肿瘤的主要手段之一,目前有许多兽药企业致力于此类抗肿瘤药的研发。本文以EMA和FDA发布的伴侣动物抗肿瘤药指导原则为依据,结合国家药品监督管理局药品审评中心(CDE)发布的抗肿瘤药物临床试验技术指导原则对比分析,对伴侣动物使用的细胞毒类抗肿瘤药研发过程中的临床试验设计关键技术要点进行了分析,旨在为伴侣动物用细胞毒类抗肿瘤药临床评价提供参考。
Neoplasia has gradually developed into the most commonly encountered disease in geriatric companion animals.Currently,there is no authorized anti-tumor drug specified using for companion animal in China.As cytotoxic antitumor drug is currently one of the main methods for treatment of malignant tumors,many veterinary drug companies are committed to do research and development for these drugs.This article is based on EMA and FDA guidelines associating with companion animal antitumor drugs in combination with the CDE's technical guidelines for clinical trials of antitumor drugs.Key technical points of clinical trial designing in research and development process of companion animal cytotoxic anti-tumor drugs were reviewed in this article and to provide reference for the clinical evaluation of cytotoxic anti-tumor drugs for companion animals.
作者
杨宇欣
刘羽
邱基程
李格宾
吴聪明
汪霞
梁先明
苏富琴
曹兴元
YANG Yu-xin;LIU Yu;QIU Ji-cheng;LI Ge-bing;WU Cong-ming;WANG Xia;LIANG Xian-ming;SU Fu-qin;CAO Xing-yuan(College of Veterinary Medicine,China Agricultural University,Beijing 100193,China;National Center for Veterinary Drug Safety Evaluation,Beijing 100193,China;China Agricultural University Veterinary Teaching Hospital,Beijing 100193,China;China Institute of Veterinary Drug Control,Beijing 100081,China)
出处
《中国兽药杂志》
2023年第3期44-50,共7页
Chinese Journal of Veterinary Drug
关键词
临床试验
伴侣动物
细胞毒类抗肿瘤药
疗效评价
clinical trial
companion animal
cytotoxic antitumor drug
efficacy evaluation
