Abaloparatide

FDA Approved

Also known as: Tymlos, BA058, PTHrP analog

Bone & Metabolic

Last reviewed: April 28, 2026

A synthetic analog of parathyroid hormone-related protein (PTHrP) FDA-approved for osteoporosis. Similar to teriparatide but with a potentially more favorable bone-building to bone-resorbing ratio and lower hypercalcemia risk.

Mechanism of Action

Selectively activates the RG conformation of the PTH1 receptor, producing a more transient signaling response than teriparatide. This results in robust bone formation with less bone resorption and less calcium mobilization from bone.

Common Uses

  • Postmenopausal osteoporosis
  • Fracture risk reduction
  • Bone density improvement

Known Risks

  • Osteosarcoma risk (boxed warning — animal studies)
  • Dizziness
  • Nausea
  • Tachycardia
  • Injection site reactions
  • Limited to 2 years of use

Regulatory Status

FDA Approved

FDA-approved as Tymlos (2017) for treatment of postmenopausal women with osteoporosis at high fracture risk. Limited to 2 years. Pen injector for daily self-administration.

Common Protocols

Protocol information is for educational reference only. Dosing varies significantly by individual, condition, and physician guidance. Always work with a licensed healthcare provider.

Subcutaneous injection

Typical Dose

80 mcg

Frequency

Once daily

Cycle Length

Up to 24 months

Self-administered via pen injector in the periumbilical region. Refrigerate pen. Follow with anti-resorptive therapy after completing course.

Related Compounds

Research References

This information is for educational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional before starting any peptide therapy. Data is compiled from published research and regulatory sources and may not reflect the most recent developments.