Stein Gold Linda, Eyerich Kilian, Merola Joseph F, Torres Joana, Coates Laura C, Allegretti Jessica R
Department of Dermatology, Henry Ford Health, Detroit, MI, USA.
Department of Dermatology, Medical Center and Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Adv Ther. 2025 May 29. doi: 10.1007/s12325-025-03213-8.
Immune-mediated inflammatory diseases (IMIDs), such as psoriasis, psoriatic arthritis, and inflammatory bowel disease, encompass a heterogenous group of conditions associated with chronic inflammation. Systemic treatments for patients with IMIDs include parenterally delivered monoclonal antibodies (mAbs) that disrupt specific cytokine and cytokine receptor binding interactions, and orally delivered small molecules that inhibit certain enzymes involved in the regulation of inflammatory signaling. Many patients prefer oral alternatives to injectables, but currently available oral advanced therapies are less effective than mAbs and/or have tolerability concerns. Thus, an unmet need exists for additional oral treatment options for patients with IMIDs. Therapeutic peptides can be designed to possess characteristics that provide both the target selectivity typically associated with parenterally delivered mAbs and an oral route of administration. Oral peptide therapeutics are an area of intense research in several therapeutic areas, and, although some oral peptides are available for certain indications, such as diabetes, there are currently no targeted oral peptides available for the treatment of patients with IMIDs. Icotrokinra (JNJ-77242113), which is currently in development to treat patients with various IMIDs, is the first targeted oral peptide designed to selectively inhibit interleukin (IL)-23 signaling by blocking the IL-23 receptor on human immune cells. In a phase 2b study in adults with moderate-to-severe psoriasis, icotrokinra showed a significant dose-response effect versus placebo, and a tolerable safety profile at Week 16. Sustained skin clearance and no safety signals were observed through Week 52 in the extension study to the phase 2b study. Ongoing phase 2 and phase 3 clinical studies in patients with psoriasis, psoriatic arthritis, and ulcerative colitis will provide data to inform the therapeutic potential of icotrokinra to address the unmet need in these diseases.
免疫介导的炎症性疾病(IMIDs),如银屑病、银屑病关节炎和炎症性肠病,是一组与慢性炎症相关的异质性疾病。针对IMIDs患者的全身治疗包括通过肠胃外给药的单克隆抗体(mAb),其可破坏特定细胞因子和细胞因子受体的结合相互作用,以及口服的小分子药物,其可抑制参与炎症信号调节的某些酶。许多患者更喜欢口服药物而非注射药物,但目前可用的口服先进疗法比单克隆抗体效果差,和/或存在耐受性问题。因此,IMIDs患者对更多口服治疗选择存在未满足的需求。治疗性肽可被设计成具有既能提供通常与肠胃外给药的单克隆抗体相关的靶点选择性又能实现口服给药途径的特性。口服肽疗法是多个治疗领域的研究热点,尽管某些口服肽可用于特定适应症,如糖尿病,但目前尚无用于治疗IMIDs患者的靶向口服肽。Icotrokinra(JNJ-77242113)目前正处于开发阶段,用于治疗各种IMIDs患者,它是首个靶向口服肽,旨在通过阻断人类免疫细胞上的白细胞介素(IL)-23受体来选择性抑制IL-23信号传导。在一项针对中度至重度银屑病成人患者的2b期研究中,Icotrokinra与安慰剂相比显示出显著的剂量反应效应,且在第16周时安全性良好。在2b期研究的扩展研究中,直至第52周均观察到持续的皮肤清除效果且无安全信号。正在进行的针对银屑病、银屑病关节炎和溃疡性结肠炎患者的2期和3期临床研究将提供数据,以了解Icotrokinra在满足这些疾病未满足需求方面的治疗潜力。