Abaloparatide Comparator Trial In Vertebral Endpoints (ACTIVE) confirms that abaloparatide is a valuable addition to the armamentarium against osteoporosis

Expert Opin Pharmacother. 2017 Dec;18(17):1811-1813. doi: 10.1080/14656566.2017.1395021. Epub 2017 Nov 14.

Abstract

The recently published Abaloparatide Comparator Trial in Vertebral Endpoints (ACTIVE) assessed the efficacy and safety of abaloparatide (80 µg daily subcutaneous) (ABL) vs placebo during 18 months, in postmenopausal osteoporosis. Teriparatide (20 µg daily subcutaneous) (TPD) was used as an open label active comparator. The results of the study suggest that ABL increases bone mineral density more than TPD and reduces major osteoporotic fractures to a greater extent than TPD with a more rapid onset of action. These outcomes combined with a positive safety profile make ABL an interesting addition to the armamentarium against postmenopausal osteoporosis.

Keywords: Abaloparatide; anabolic agents; fracture; hypercalcemia; osteoporosis; parathyroid hormone; teriparatide.

MeSH terms

  • Aged
  • Bone Density Conservation Agents / pharmacology
  • Bone Density Conservation Agents / therapeutic use*
  • Female
  • Humans
  • Osteoporosis / drug therapy*
  • Parathyroid Hormone-Related Protein / pharmacology
  • Parathyroid Hormone-Related Protein / therapeutic use*

Substances

  • Bone Density Conservation Agents
  • Parathyroid Hormone-Related Protein
  • abaloparatide