Salamat Ali Jawad, Salamat Ali Tooba, Al Hasibuzzaman Md
Department of Gastroenterology, Shaikh Khalifa Bin Zayed Al Nahyan Medical & Dental College, Lahore, Pakistan.
Department of Pharmacology & Therapeutics, Gujranwala Medical College, Gujranwala, Pakistan.
Ann Med Surg (Lond). 2025 Jan 9;87(1):30-32. doi: 10.1097/MS9.0000000000002868. eCollection 2025 Jan.
Elafibranor (Iqirvo) has recently received FDA approval for treating primary biliary cholangitis (PBC) in combination with ursodeoxycholic acid (UDCA). This novel drug, a dual peroxisome proliferator-activated receptor-α/δ agonist, addresses the unmet need in PBC patients unresponsive to UDCA alone. Clinical trials, particularly the ELATIVE study, have shown significant biochemical improvements, including reduced alkaline phosphatase (ALP) levels and optimized lipid profiles. While common side effects include gastrointestinal discomfort, more severe but rare adverse effects, such as muscle injury and new-onset cholelithiasis, were observed. Elafibranor represents a promising advance in PBC management, offering enhanced efficacy with a tolerable safety profile. However, further research is needed to assess its long-term effectiveness and safety.
艾拉非布诺(Iqirvo)最近获得了美国食品药品监督管理局(FDA)的批准,可与熊去氧胆酸(UDCA)联合用于治疗原发性胆汁性胆管炎(PBC)。这种新型药物是一种过氧化物酶体增殖物激活受体-α/δ双重激动剂,满足了单独使用UDCA无反应的PBC患者未被满足的需求。临床试验,尤其是ELATIVE研究,已显示出显著的生化改善,包括碱性磷酸酶(ALP)水平降低和血脂谱优化。虽然常见副作用包括胃肠道不适,但也观察到了更严重但罕见的不良反应,如肌肉损伤和新发胆石症。艾拉非布诺在PBC治疗方面代表了一项有前景的进展,具有增强的疗效和可耐受的安全性。然而,需要进一步研究来评估其长期有效性和安全性。