Promising phase II biologics for future Crohn's disease therapy

被引:2
|
作者
Wils, Pauline [1 ,2 ,7 ]
Danese, Silvio [3 ,4 ]
Peyrin-Biroulet, Laurent [5 ,6 ]
机构
[1] Univ Lille 2, Claude Huriez Hosp, Dept Gastroenterol, Lille, France
[2] Univ Lille, Inserm, CHU Lille, U1286 INFIN Inst Translat Res Inflammat, Lille, France
[3] IRCCS Osped San Raffaele, Gastroenterol & Endoscopy, Milan, Italy
[4] Univ Vita Salute San Raffaele, Milan, Italy
[5] Univ Lorraine, Dept Gastroenterol, CHRU Nancy, Nancy, France
[6] Univ Lorraine, Inserm, Nancy, France
[7] Ctr Hosp Claude Huriez, Serv Malad Appareil Digest, 1 Rue Michel Polonovski, F-59000 Lille, France
关键词
biologics; Crohn's disease; inflammatory bowel diseases; Phase II; randomized trials; INFLAMMATORY-BOWEL-DISEASE; MAINTENANCE THERAPY; ULCERATIVE-COLITIS; EXPRESSION; SAFETY; METAANALYSIS; USTEKINUMAB; INDUCTION; ADDRESSIN; EFFICACY;
D O I
10.1080/13543784.2023.2219386
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionAlthough the physician's therapeutic arsenal of Crohn's Disease (CD) is rapidly expanded over the next 25 years, a significant proportion of patients remain non-responders, or develop a loss of response or intolerance to current therapies, indicating a need for new therapeutic strategies in CD.Areas coveredThis review examines the efficacy and safety data from phase II clinical trials on biologics, performed in patients with moderate-to-severe CD. A PubMed database literature review was conducted for relevant articles published from 2017 to 2022. Ongoing clinical phase II trials were retrieved from ClinicalTrials.gov database or abstracts from major congresses. Future perspectives for the treatment of CD patients with these new molecules were also discussed.Expert opinionAmong the most promising biologics are interleukin (IL)-23p19 inhibitors (guselkumab, mirikizumab, and brazikumab), IL-6 inhibitors, and anti-adhesion molecules (ontamalimab). Furthermore, multiple biologics with different mechanisms of action are in clinical development for moderate-to-severe CD including molecules with anti-fibrotic mechanism of action (anti-TL1A, anti-IL-36 receptor). In addition to efficacy, some of them provide reassuring safety profiles. Phase III trials need to confirm these results, especially on their long-term safety issues.
引用
收藏
页码:495 / 507
页数:13
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