Abaloparatide CAS:247062-33-5
Abaloparatide is indicated for the treatment of osteoporosis, specifically in postmenopausal women who are at high risk for fractures. Osteoporosis is a condition characterized by low bone mass and microarchitectural deterioration of bone tissue, leading to increased bone fragility and susceptibility to fractures. Postmenopausal women are particularly vulnerable to osteoporotic fractures due to estrogen deficiency, which accelerates bone loss. Abaloparatide works by stimulating bone formation through its selective activation of the parathyroid hormone receptor (PTH1 receptor). Unlike traditional treatments for osteoporosis, such as bisphosphonates, which primarily inhibit bone resorption, Abaloparatide promotes bone formation by increasing osteoblast activity and bone mineral density. Clinical studies have demonstrated that Abaloparatide significantly reduces the risk of vertebral and nonvertebral fractures in postmenopausal women with osteoporosis. Its efficacy in improving bone density and strength contributes to enhanced skeletal integrity and reduced fracture incidence over time. The administration of Abaloparatide involves daily subcutaneous injections, allowing for consistent delivery of the medication to support bone remodeling and mineralization. This treatment regimen is well tolerated by most patients and offers a convenient option for long-term management of osteoporosis. In addition to fracture prevention, Abaloparatide helps improve quality of life by reducing the pain and disability associated with osteoporotic fractures. By enhancing bone strength and resilience, it supports mobility and independence in affected individuals, thereby mitigating the socioeconomic burden of osteoporosis-related complications. Overall, Abaloparatide represents an important advancement in the therapeutic landscape for osteoporosis, offering a targeted approach to bone health management in postmenopausal women at high risk for fractures. Its ability to stimulate bone formation and reduce fracture risk underscores its role as a valuable treatment option, potentially enhancing long-term skeletal health and quality of life for patients affected by osteoporosis. Ongoing research continues to explore its safety profile and efficacy in broader patient populations, further solidifying its place in osteoporosis management strategies.
Composition | C174H300N56O49 |
Assay | 99% |
Appearance | white powder |
CAS No. | 247062-33-5 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |