Teriparatide

FDA Approved

Also known as: Forteo, PTH 1-34, Parathyroid Hormone Fragment

Bone & Metabolic

Last reviewed: April 28, 2026

A recombinant fragment of parathyroid hormone (amino acids 1-34) FDA-approved for osteoporosis. The first anabolic (bone-building) agent approved for osteoporosis, as opposed to anti-resorptive drugs that only slow bone loss.

Mechanism of Action

Intermittent exposure to PTH(1-34) paradoxically stimulates osteoblast activity more than osteoclast activity, resulting in net bone formation. This is opposite to the bone-resorbing effect of continuously elevated PTH in hyperparathyroidism.

Common Uses

  • Severe osteoporosis
  • Fracture risk reduction
  • Glucocorticoid-induced osteoporosis
  • Bone healing acceleration

Known Risks

  • Osteosarcoma risk (boxed warning — based on rat studies at high doses)
  • Hypercalcemia
  • Orthostatic hypotension
  • Leg cramps
  • Nausea
  • Limited to 2 years of use

Regulatory Status

FDA Approved

FDA-approved as Forteo (2002) for osteoporosis in postmenopausal women and men at high fracture risk. Limited to 2 years of treatment due to theoretical osteosarcoma risk. Biosimilar (Tymlos/abaloparatide is a related but distinct peptide).

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

20 mcg

Frequency

Once daily

Cycle Length

Up to 24 months (FDA limit)

Self-administered via pen injector in the thigh or abdomen. Must be refrigerated. Follow with anti-resorptive therapy after completing course to maintain bone gains.

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.