Current status of drugs in development for celiac disease

被引:10
|
作者
Kurppa, Kalle [1 ,2 ]
Hietikko, Minna [1 ,2 ]
Sulic, Ana-Marija [1 ,2 ]
Kaukinen, Katri [3 ,4 ,5 ]
Lindfors, Katri [1 ,2 ]
机构
[1] Univ Tampere, Tampere Ctr Child Hlth Res, Tampere 33520, Finland
[2] Tampere Univ Hosp, Tampere 33520, Finland
[3] Univ Tampere, Sch Med, Tampere 33520, Finland
[4] Tampere Univ Hosp, Dept Internal Med, Tampere 33520, Finland
[5] Seinajoki Cent Hosp, Dept Internal Med, Seinajoki, Finland
基金
芬兰科学院;
关键词
gluten; pharmacotherapy; small intestine; synthetic drug; GLUTEN-FREE DIET; COMBINATION ENZYME THERAPY; PLACEBO-CONTROLLED TRIAL; TRANSGLUTAMINASE TYPE-II; SEED STORAGE PROTEINS; PROOF-OF-CONCEPT; AT-RISK GROUPS; LARAZOTIDE ACETATE; GLIADIN PEPTIDES; ANTIGEN PRESENTATION;
D O I
10.1517/13543784.2014.916274
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Gluten is the main trigger for celiac disease, and the current treatment is based on its elimination from the diet. Although the symptoms usually disappear during the diet, it is restrictive and difficult to maintain. Further, despite a strict treatment the small-bowel mucosal damage does now always heal. Consequently, adherence is often poor and new treatment approaches are needed. With an increased understanding of the disease pathogenesis, several novel treatments have been suggested, and some of them have already entered Phase II clinical trials. Areas covered: This article reviews the latest status of the drugs in development for celiac disease. The article focuses mainly on synthetic drugs currently entering in clinical trials. Expert opinion: It is anticipated that some of the treatments under investigation will soon enter Phase III clinical trials, although challenges remain. For instance, histological studies are problematic in wide-scale clinical studies. On the other hand, the existing non-invasive serological methods and clinical outcome measures might be too insensitive for monitoring responses to the possible drug candidates. There is also no animal model which would accurately reflect celiac disease. Well-conducted basic and clinical research is required to develop better non-invasive surrogate markers and patient-related outcomes for future pharmacological studies.
引用
收藏
页码:1079 / 1091
页数:13
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