New Mexico Clinical Research & Osteoporosis Center, Albuquerque, New Mexico 87106, USA.
Expert Opin Biol Ther. 2011 Jan;11(1):117-27. doi: 10.1517/14712598.2011.540565. Epub 2010 Nov 29.
Osteoporosis is a common skeletal disease characterized by loss of bone strength that leads to increased risk of fractures. Fractures of the hip and spine are associated with disability, increased risk of death and high healthcare costs. Recent improvement in the understanding of the molecular regulators of bone metabolism has led to the investigation and development of new therapeutic agents with novel mechanisms of action that may offer advantages over currently available treatments for osteoporosis.
Sclerostin is a small protein secreted by osteocytes that downregulates osteoblast-mediated bone formation. This is a review of the rationale, mechanism of action, preclinical and clinical development of AMG 785 (CDP7851), an investigational humanized mAb that inhibits the activity of sclerostin, resulting in increased bone formation.
The reader will gain an insight into the potential use of sclerostin mAb therapy for the treatment of osteoporosis.
Preclinical studies and an early report of a clinical study suggest that inhibition of sclerostin with AMG 785 may provide skeletal benefit for patients with osteoporosis.
骨质疏松症是一种常见的骨骼疾病,其特征是骨强度丧失,导致骨折风险增加。髋部和脊柱骨折与残疾、死亡风险增加和高医疗保健费用有关。最近对骨代谢分子调节剂的理解的提高,导致了对新的治疗药物的研究和开发,这些药物具有新的作用机制,可能比目前可用的骨质疏松症治疗方法具有优势。
硬骨素是一种由骨细胞分泌的小蛋白,可下调成骨细胞介导的骨形成。这是一篇关于 AMG 785(CDP7851)的基本原理、作用机制、临床前和临床开发的综述,AMG 785 是一种研究性的人源化单克隆抗体,可抑制硬骨素的活性,从而增加骨形成。
读者将深入了解硬骨素单克隆抗体治疗骨质疏松症的潜在用途。
临床前研究和一项早期的临床研究报告表明,用 AMG 785 抑制硬骨素可能为骨质疏松症患者提供骨骼益处。