Advancing therapeutic frontiers: a pipeline of novel drugs for UC management.

Luisa Bertin, Alessandro Massano, Carlo Redavid, Marco Scarpa, Cesare Ruffolo, Imerio Angriman, Andrea Buda, Fabiana Zingone, Brigida Barberio, Edoardo Vincenzo Savarino
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Abstract

Ulcerative colitis is a chronic inflammatory bowel disease with rising global prevalence. Despite therapeutic advances including biologic agents targeting tumor necrosis factor-alpha, integrins, and interleukin pathways, alongside Janus kinase inhibitors and sphingosine-1-phosphate receptor modulators, substantial unmet needs persist in moderate to severe disease. Current advanced therapies achieve clinical response rates of only 30-60% in trials, with approximately 20% of patients requiring hospitalization and 7% undergoing colectomy within five years of diagnosis. The therapeutic pipeline for moderate to severe ulcerative colitis currently encompasses over 100 investigational agents in Phase II and III clinical development. Emerging mechanisms include next-generation Janus kinase and tyrosine kinase 2 inhibitors with enhanced selectivity, novel cell trafficking modulators, advanced tumor necrosis factor-alpha inhibition strategies, and selective interleukin-23 pathway antagonists. Tumor necrosis factor-like ligand 1A pathway inhibitors demonstrate particularly robust efficacy in early trials, with clinical remission rates exceeding 25% compared to less than 2% for placebo. Additional promising approaches target immune checkpoint pathways, receptor-interacting protein kinase 1, and intracellular signaling cascades. innovative combination therapy approaches demonstrated to achieve superior response rates compared to monotherapy. The convergence of novel therapeutic targets, gut-selective compounds minimizing systemic immunosuppression, and biomarker-guided therapy selection represents a paradigm shift toward precision medicine. These advances hold genuine promise for transforming moderate to severe ulcerative colitis management.

推进治疗前沿:UC管理的新药管道。
溃疡性结肠炎是一种慢性炎症性肠病,全球患病率不断上升。尽管治疗进展包括靶向肿瘤坏死因子- α、整合素和白介素途径的生物制剂,以及Janus激酶抑制剂和鞘氨醇-1-磷酸受体调节剂,但在中度至重度疾病中仍存在大量未满足的需求。目前的先进疗法在临床试验中仅达到30-60%的临床缓解率,大约20%的患者需要住院治疗,7%的患者在诊断后的五年内接受结肠切除术。目前,中度至重度溃疡性结肠炎的治疗管道包括超过100种处于II期和III期临床开发的研究药物。新出现的机制包括选择性增强的下一代Janus激酶和酪氨酸激酶2抑制剂、新型细胞运输调节剂、晚期肿瘤坏死因子α抑制策略和选择性白介素-23途径拮抗剂。肿瘤坏死因子样配体1A途径抑制剂在早期试验中表现出特别强劲的疗效,临床缓解率超过25%,而安慰剂的缓解率不到2%。其他有希望的方法包括免疫检查点通路、受体相互作用蛋白激酶1和细胞内信号级联。与单一治疗相比,创新的联合治疗方法显示出更高的缓解率。新的治疗靶点、减少全身免疫抑制的肠道选择性化合物和生物标志物引导的治疗选择的融合代表了向精准医学的范式转变。这些进步为转变中度至重度溃疡性结肠炎的治疗带来了真正的希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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