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Bone Health
Clinical

Abaloparatide

Also known as: Tymlos, Eladynos, BA058

A synthetic PTHrP analog that builds bone, FDA-approved as Tymlos for osteoporosis at high fracture risk. Prescription medication.

Last updated

Mechanism of Action

Abaloparatide is a 34-amino-acid synthetic analog of parathyroid hormone-related protein (PTHrP 1-34) that activates the PTH type 1 receptor (PTH1R) on osteoblasts. It binds preferentially to the receptor's RG conformation, producing shorter cAMP signaling than PTH. Given as a once-daily pulse, this favors bone formation over resorption, raising bone mineral density and lowering fracture risk.

Half-life
~1.7 hours
Administration Routes
Subcutaneous
Research Status
Clinical

Reported Benefits

  • Reduces new vertebral fractures in postmenopausal women with osteoporosis
  • Reduces nonvertebral fractures versus placebo in the ACTIVE trial
  • Increases bone mineral density in men with osteoporosis at high fracture risk
  • Typically followed by an antiresorptive to maintain gains

Potential Side Effects

  • Orthostatic hypotension and dizziness, mostly after early doses
  • Hypercalcemia and hypercalciuria (kidney stone risk)
  • Nausea, headache and palpitations or fast heart rate
  • Osteosarcoma in rat studies (the former boxed warning was removed in 2021)

Common Dosing

Labeled dosing is 80 mcg injected subcutaneously into the abdomen once daily, with calcium and vitamin D supplementation if dietary intake is inadequate. The label states that use for more than 2 years during a patient's lifetime is not recommended. Dosing is set and supervised by the prescribing clinician.

The dosing information above is aggregated from research literature and anecdotal community reports for educational purposes only. It is not a recommendation, prescription, or medical advice. Peptides are sold as research chemicals only and are not intended for human use.

Contraindications

  • Increased baseline osteosarcoma risk (Paget's disease, open epiphyses, prior skeletal radiation): avoid
  • Pre-existing hypercalcemia or hyperparathyroidism
  • Active or recent kidney stones (use with caution)

No documented stacking partners for Abaloparatide yet.

  • Effect of Abaloparatide vs Placebo on New Vertebral Fractures in Postmenopausal Women With Osteoporosis: A Randomized Clinical Trial

    2016

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  • The Efficacy and Safety of Abaloparatide-SC in Men With Osteoporosis: A Randomized Clinical Trial

    2022

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  • Fracture and Bone Mineral Density Response by Baseline Risk in Patients Treated With Abaloparatide Followed by Alendronate: Results From the Phase 3 ACTIVExtend Trial

    2019

    View

Yes. The FDA approved it as Tymlos in April 2017 for postmenopausal women with osteoporosis at high risk for fracture, and expanded the label in December 2022 to men with osteoporosis at high fracture risk. It is a prescription medication used under medical supervision.

Both are daily anabolic injections that act on the PTH1R receptor. Abaloparatide is based on PTHrP and teriparatide on PTH; the ACTIVE trial included an open-label teriparatide arm, but the two were not formally compared head to head for fracture outcomes.

Bone gains are generally maintained by switching to an antiresorptive drug such as alendronate, as studied in the ACTIVExtend trial. The follow-on plan is chosen by the treating clinician.

PeptideChat is for educational and research purposes only. Nothing on this site constitutes medical advice. Peptides are sold as research chemicals only and are not intended for human use. These statements have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease. PeptideChat is an independent educational resource — not a pharmacy, compounding, or 503A/503B outsourcing facility — and does not sell products or provide medical advice.