ApprovedClinical / approved drugSubcutaneousEvidence 4/5

Abaloparatide

Also known as: Tymlos

Abaloparatide is a PTHrP(1-34) analog that agonizes the PTH1 receptor with preference for its transient RG conformation, activating cAMP signaling to stimulate osteoblast-driven new bone formation.

Abaloparatide
Drug class
Anabolic osteoporosis agent (PTHrP analog)
Primary targets
PTH1 receptor (PTH1R)
Dose reference
FDA label reference dose: 80 mcg subcutaneously once daily (a labeled dose, not a recommendation)
Half-life
Approximately 1-1.7 hours (FDA label)
Developer / origin
Invented at Ipsen (BA058); developed and marketed by Radius Health as Tymlos
Reference year
2017
Evidence score
4/5 - Strong approval-grade clinical evidence

Approved uses

  • Treatment of postmenopausal women with osteoporosis at high risk for fracture
  • Treatment of men with osteoporosis at high risk for fracture
Evidence 4/5

Strong approval-grade clinical evidence

Abaloparatide is FDA-approved with phase 3 randomized trial support: ACTIVE showed reduced vertebral and nonvertebral fractures versus placebo in postmenopausal women, ACTIVExtend supported sequential maintenance benefit, and ATOM supported the male bone-density indication. Evidence is robust for women's fracture endpoints and solid but density-based for men.

Investigational compound with human randomized or phase 2/3 evidence.

Evidence basis

  • ACTIVE phase 3 RCT (JAMA 2016, n=2463) showed significant vertebral and nonvertebral fracture reduction vs placebo
  • ACTIVExtend demonstrated continued benefit with sequential alendronate
  • ATOM phase 3 RCT (n=228) supported the 2022 male indication via bone mineral density
  • FDA approvals 2017 (women) and 2022 (men) with DailyMed labeling
  • Male approval rests on BMD rather than a fracture-endpoint trial, a noted limit

How to read this entry

Dose references and half-life values are pulled from trial protocols, labels, reviews, or published summaries where available. They are context for research and comparison, not a personal dosing recommendation.

Status matters: approved drugs have regulated indications; investigational compounds are still being studied; research-only peptides do not have established human dosing, safety, or efficacy for consumer use.

Abaloparatide guides

Read the matching guide or adjacent research pages for more context.

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