New and Evolving Therapies for Cystic Fibrosis Patients

被引:0
|
作者
Jabar, Alisha [1 ]
Raissy, Hengameh H. [2 ]
Blake, Kathryn [3 ]
机构
[1] Univ New Mexico, Dept Pediat, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Hlth Sci Ctr, Dept Pediat, Sch Med, Albuquerque, NM 87131 USA
[3] Nemours Childrens Clin, Biomed Res Dept Floor 1, Jacksonville, FL USA
关键词
MUTATION; ADHERENCE;
D O I
10.1089/ped.2014.0364
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Cystic fibrosis (CF) is a common autosomal recessive inherited disorder affecting 1 in 2,500 births and similar to 75,000 people in North America, Europe, and Australia. The purpose of this review is to discuss the most recent advances in therapies for CF patients. The CF drug development pipeline provides information regarding the phase of each new therapy and those that are already in use by patients. The ultimate goal of therapy will be to deliver tailored individualized therapies to those who need it the most. This review will focus on new research on CF transmembrane conductance regulator protein modulator agents and the effort of gene therapy.
引用
收藏
页码:92 / 94
页数:3
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