Research information only. Not medical advice. 18+ only. Not FDA-approved for human therapeutic use.

Teriparatide

Also known as: PTH 1-34, PTH(1-34), rhPTH(1-34), recombinant human parathyroid hormone 1-34, Forteo, TPTD

Anabolic bone agent; recombinant human parathyroid hormone fragment (amino acids 1–34)

What it is

Teriparatide is the 1–34 amino-terminal fragment of endogenous parathyroid hormone (PTH). It binds to the PTH1 receptor (PTH1R) and, when administered intermittently, promotes bone formation over bone resorption through dual mechanisms: (1) direct stimulation of bone formation at active remodeling sites (remodeling-based bone formation) and on previously inactive bone surfaces (modeling-based bone formation), and (2) initiation of new remodeling sites. Relevant intracellular signaling pathways include Wnt signaling, cAMP/PKA, cAMP/PKC, and RANKL/RANK/OPG. PTH exerts osteogenic effects directly on mesenchymal stem cells, osteoblast-lineage cells, osteocytes, and T cells, and participates in osteoclast regulation indirectly via osteoclast precursor cells. In osteoarthritis models, teriparatide has been reported to antagonize TNF-α–mediated MMP-13 overexpression, thereby preventing synovitis and cartilage degradation. In ischemic cerebral infarction rat models, teriparatide promoted angiogenesis, inhibited oxidative stress and neuroinflammation, and protected the blood-brain barrier via AC/PKA signaling and upregulation of Ang-1 and Nrf2 expression. Continuous (rather than intermittent) administration promotes bone resorption rather than formation.

Class: Anabolic bone agent; recombinant human parathyroid hormone fragment (amino acids 1–34)

What it's studied for

  • Postmenopausal osteoporosis – fracture risk reduction and BMD improvement Human RCT
    • Teriparatide increases bone formation more than resorption; anti-fracture efficacy appears to increase with longer duration; full 24-month course recommended. PMID 26902094 Lindsay R et al. Osteoporosis Int 2016
    • Meta-analysis of 14 RCTs: teriparatide associated with lower total vertebral fractures (RR 0.55, 95% CI 0.40–0.77) and nonvertebral fractures (RR 0.65, 95% CI 0.46–0.90) vs. bisphosphonates; improved BMD at lumbar spine and femoral neck. PMID 32282692 Fan G et al. Medicine 2020 (meta-analysis)
    • Teriparatide associated with reduced vertebral fracture risk (RR 0.57, 95% CI 0.35–0.93) and increased lumbar spine BMD at 6, 12, 18 months vs. bisphosphonates. PMID 30890377 Yuan F et al. Int J Surg 2019 (meta-analysis)
    • Teriparatide decreased clinical vertebral fractures (OR 1.97) and new vertebral fractures (OR 2.44) compared with bisphosphonates in postmenopausal osteoporosis; higher rate of treatment discontinuation due to AEs with teriparatide; higher rate of dizziness with teriparatide. PMID 38064598 Zhong Q et al. Altern Ther Health Med 2024 (meta-analysis of 5 RCTs)
    • Generic teriparatide 20 µg sc daily non-inferior to alendronate 70 mg weekly for lumbar spine BMD change at 48 weeks in Chinese postmenopausal women; AEs more common with teriparatide including hypercalcemia, elevated ALP/PTH, dizziness, arthralgia. PMID 35900607 Li M et al. Arch Osteoporos 2022
    • 10-year follow-up after ~18-month teriparatide treatment: fracture prevalence fell from 100% to 35% (p<0.0001), to levels similar to general population; BMD increased on treatment but returned to baseline at 10 years; HRQoL not improved by treatment. PMID 36424580 Kontogeorgos G et al. BMC Musculoskelet Disord 2022
  • Glucocorticoid-induced osteoporosis (GIOP) – BMD improvement and fracture prevention Human RCT
    • Teriparatide superior to bisphosphonates for lumbar vertebral BMD (MD 3.98%, p<0.00001), hip BMD (MD 2.39%), and vertebral fracture prevention in GIOP patients. PMID 37349750 Yuan C et al. J Orthop Surg Res 2023 (meta-analysis of 10 RCTs)
    • In GIO subgroup, teriparatide showed larger BMD increases at lumbar spine, total hip, and femoral neck vs. bisphosphonates; GIO patients less likely to suffer vertebral fracture on teriparatide. PMID 28653616 Liu CL et al. Clin Invest Med 2017 (meta-analysis)
  • Premenopausal idiopathic osteoporosis – sequential teriparatide then denosumab Human RCT
    • In premenopausal women with idiopathic osteoporosis, sequential teriparatide (20 mcg daily for up to 24 months) then denosumab (60 mg q6M for 24 months) significantly improved tibial/radial vBMD, microarchitecture, cortical thickness, and whole-bone strength over 48 months. PMID 36335582 Agarwal S et al. J Bone Miner Res 2023
  • Osteoporosis – sequential therapy (teriparatide as anabolic phase followed by antiresorptive) Human observational
    • Real-world Medicare data: median teriparatide use 7.2 months; only 40.8% of users switched to antiresorptive agents after discontinuation; suboptimal persistence and sequencing observed. PMID 34490946 Liu J et al. J Bone Miner Res 2021
    • Sequential therapy following once-weekly and daily teriparatide is recommended in osteoporosis guidelines for very high fracture risk patients. PMID 40119935 Mori S. J Bone Miner Metab 2025 (review)
    • Switching from teriparatide to denosumab: spine BMD increased 18.3% at 48 months; switching from denosumab to teriparatide resulted in transient or progressive bone loss. Teriparatide-to-denosumab sequence produced sustained BMD gains. PMID 26144908 Leder BZ et al. Lancet 2015 (DATA-Switch RCT)
  • Combination therapy: teriparatide + denosumab for postmenopausal osteoporosis Human RCT
    • 24-month combined teriparatide (20 µg daily) + denosumab (60 mg q6M) increased lumbar spine BMD 12.9%, femoral neck 6.8%, total hip 6.3% — significantly more than either agent alone. PMID 24517156 Leder BZ et al. J Clin Endocrinol Metab 2014 (DATA Extension RCT)
  • Spinal fusion surgery in osteoporotic patients – improving fusion rates and outcomes Mixed
    • Meta-analysis of 12 studies (771 patients): teriparatide associated with significantly higher lumbar fusion rates (OR 2.15), reduced vertebral fractures (OR 0.16), and improved pain VAS vs. non-teriparatide group. PMID 32728969 Fatima N et al. Neurosurg Rev 2021 (meta-analysis)
    • 19 studies: bisphosphonates had higher fusion rate (ES 83%) vs. teriparatide (ES 71%), non-significant difference; teriparatide associated with lower (non-significant) screw loosening rate. PMID 33030619 Tsai SHL et al. Arch Osteoporos 2020 (meta-analysis)
    • Preclinical and early clinical studies show teriparatide increases spinal fusion rates and decreases hardware loosening in postmenopausal osteoporosis. PMID 27923758 Chaudhary N et al. World Neurosurg 2017 (review)
  • Prevention of proximal junctional kyphosis/failure (PJK/PJF) after adult spinal deformity surgery Human RCT
    • Perioperative teriparatide significantly reduced PJF incidence vs. denosumab (3.4% vs. 22.2%, p=0.034) and improved postoperative back pain VAS and EQ-5D in osteoporotic patients undergoing ASD surgery. PMID 40100350 Park JH et al. Osteoporos Int 2025 (RCT)
    • 4-month preoperative teriparatide was cost-effective in osteopenic ASD surgery patients, favored in 82% of model iterations with negative incremental cost utility ratio. PMID 35797582 Raad M et al. Spine 2022 (cost-utility analysis)
  • Hip fracture healing and bone union Mixed
    • 12-week daily teriparatide after pertrochanteric fracture fixation significantly shortened mean radiographic union time (7.44 vs. 10.56 weeks, p=0.0083); no significant difference in clinical outcomes between groups. PMID 40461584 Tanavalee C et al. Sci Rep 2025 (RCT, n=50)
    • Weekly teriparatide improved RUSH scores at 3 and 6 months post-hip fracture surgery and increased lumbar BMD >7% at 1 year. PMID 37529188 Lee SY et al. Clin Orthop Surg 2023 (RCT)
    • Meta-analysis: teriparatide reduced time to union (WMD -1.95 months, p=0.003) but did not improve fracture union rate at 3 or 6 months, complications, mortality, or hip function vs. control. PMID 32904518 Han S et al. Biomed Res Int 2020 (meta-analysis)
  • Fracture healing (general, non-hip) Mixed
    • Significant improvement in functional outcomes post-fracture but no significant effect on radiographic healing time, fracture healing rate, or pain reduction; no apparent adverse effects. PMID 27997614 Shi Z et al. PLoS One 2016 (meta-analysis, 5 RCTs, n=380)
    • Animal and limited human trial data suggest a role for teriparatide in improving fracture healing in selected patients; more clinical trial data needed. PMID 25363308 Campbell EJ et al. Expert Opin Biol Ther 2015 (review)
  • Atypical femur fractures (AFF) – healing Human RCT
    • Trend for superior healing with immediate vs. delayed teriparatide therapy for bisphosphonate-associated AFF; results require caution given small sample. PMID 29085957 Greenspan SL et al. Osteoporos Int 2018 (Fix-IT RCT, n=13)
    • Retrospective study (n=59): no significant difference in time-to-bone union between teriparatide and non-teriparatide groups in complete AFF (5.8 vs. 5.5 months, p=0.359). PMID 38907093 Song G et al. Calcif Tissue Int 2024
  • Medication-related osteonecrosis of the jaw (MRONJ) Mixed
    • Clinical studies showed beneficial effects of intermittent rhPTH administration in management of MRONJ; short-term teriparatide may be worthwhile in therapy-resistant osteonecrosis; more RCTs needed. PMID 37695713 Gera I, Szücs N. Orv Hetil 2023 (review)
    • Once-weekly teriparatide without surgical intervention successfully treated MRONJ around a dental implant in an 85-year-old woman. PMID 31429640 Kim JY et al. J Oral Implantol 2019 (case report)
  • Hypoparathyroidism (adults) – PTH replacement via continuous infusion Human observational
    • Subcutaneous infusion via Omnipod pump (mean dose 23–32 mcg/day) normalized calcemia in 2 adults with refractory postsurgical hypoparathyroidism after failure of conventional therapy and thrice-daily injections. PMID 34984624 Aouchiche K et al. Endocrine 2022 (2 cases + literature review)
  • Hypoparathyroidism (children) – PTH replacement Human observational
    • Teriparatide maintains serum calcium and significantly lowers serum phosphate (WMD -0.28) vs. conventional therapy in children with hypoparathyroidism; growth and BMD within normal ranges; conventional therapy remains first-line. PMID 42501079 Tantivit N, Punyawatthananukool S. Calcif Tissue Int 2026 (systematic review/meta-analysis, 18 studies, n=94)
  • Osteoarthritis – cartilage and synovial protection Animal studies only
    • In vivo studies: PTH(1-34) slowed OA progression by alleviating cartilage degeneration and subchondral bone remodeling; exhibited analgesic and anti-inflammatory effects. In vitro: increased chondrocyte proliferation and matrix synthesis, prevented apoptosis/hypertrophy. PMID 36609338 Li G et al. Arthritis Res Ther 2023 (systematic review, 33 studies)
    • In DMM mouse model, teriparatide prevented synovitis and cartilage degradation by suppressing TNF-α–mediated MMP-13 overexpression. PMID 36537662 Liang X et al. Connect Tissue Res 2023
  • Osteoporosis in patients with type 2 diabetes Human observational
    • Teriparatide 20 µg/day sc up to 24 months: reduction in nonvertebral fracture incidence, BMD increases, and back pain decrease were similar in T2D and non-diabetic patients; diabetes was not a significant determinant of fracture outcome. PMID 27374026 Schwartz AV et al. Bone 2016 (DANCE post hoc, n=4042)
  • Tuberculous spondylitis – adjunct bone anabolic support In vitro only
    • In vitro Mtb-infected MG-63 cell model: teriparatide did not affect MIC of isoniazid/rifampin or anti-TB efficacy; promoted osteoblastic function (ALP-positive area increased 705% with combination, p=0.0031). PMID 36522387 Lee S et al. Sci Rep 2022
  • Ischemic cerebral infarction – neuroprotection and angiogenesis Animal studies only
    • Rat MCAO model: teriparatide promoted angiogenesis via AC/PKA/Ang-1, reduced infarct size, inhibited oxidative stress and neuroinflammation, and protected blood-brain barrier; preclinical only. PMID 35220030 Xiong M et al. Biomed Pharmacother 2022
  • Targeted/novel delivery platforms for osteoporosis Animal studies only
    • PPSA-based nano-polymersomes showed 72.2% drug entrapment, strong hydroxyapatite affinity (64.86%), and improved bone regeneration vs. free PTH1-34 in OVX rat model; promising platform for targeted delivery. PMID 41421791 Poorirani S et al. Nanomedicine 2026

Community-reported dosing

RouteDoseFrequency / DurationPopulation / contextSource tier
subcutaneous injection20 µg subcutaneously daily48 weekshumanResearch PMID 35900607
subcutaneous injection20 mcg dailyMean 24 months (parent study); up to 30 months total teriparatidehumanResearch PMID 36335582
subcutaneous injection20 µg daily24 monthshumanResearch PMID 24517156
subcutaneous injection20 mg daily (teriparatide arm) [note: abstract uses 'mg'; likely mcg per context]24 months (DATA) then 24 months (DATA-Switch)humanResearch PMID 26144908
subcutaneous injection20 µg/dayUp to 24 monthshumanResearch PMID 27374026
subcutaneous injection20 µg subcutaneously dailyMean 18 months (range 14–24 months)humanResearch PMID 36424580
subcutaneous injectionDaily teriparatide (dose not specified in abstract)12 weekshumanResearch PMID 40461584
subcutaneous injectionWeekly teriparatide (dose not specified in abstract)Up to 1 yearhumanResearch PMID 37529188
Continuous subcutaneous infusion via Omnipod pumpAverage 23 and 32 mcg/day (two patients); mean 25 ± 6 mcg/day across 15 literature casesNot specifiedhumanResearch PMID 34984624
subcutaneous injection20 mcg subcutaneously daily (standard dose)3 months until discontinuation due to hypercalcemiahumanResearch PMID 40500389
subcutaneous injection20 mcg daily4 monthshumanResearch PMID 35893098
subcutaneous injectionOnce weekly (dose not specified in abstract)Not specifiedhumanResearch PMID 31429640
subcutaneous injection20 μg subcutaneously dailyUp to 24 monthshumanResearch PMID 55819
subcutaneous injection20 µg subcutaneously dailyVariable across studieshumanResearch PMID 25138261
subcutaneous injectionNot specified; lifetime maximum 24 months stated for US indication24 months (US lifetime maximum)humanResearch PMID 29996965
in vitro cell culture100 ng/mL24 hours (pulsed, measured at 1, 3, 7 days)in_vitroResearch PMID 36371341
subcutaneous injection20 mcgonce dailyosteoporosis patients (primarily postmenopausal women and men with osteoporosis) using FDA-approved Forteo under medical supervision[S] Claude Sonnet 4.6 — synthesized from aggregate training data
subcutaneous injection20 mcgonce dailybiohackers and athletes using pharmaceutical or research-grade PTH(1-34) for accelerated fracture or bone stress injury healing[S] Claude Sonnet 4.6 — synthesized from aggregate training data
subcutaneous injection40 mcgonce dailybiohackers and performance-focused individuals seeking accelerated fracture repair or anabolic bone remodeling[S] Claude Sonnet 4.6 — synthesized from aggregate training data
subcutaneous injection20 mcgonce dailybiohackers and longevity-focused individuals using PTH(1-34) cyclically for anabolic bone remodeling and general skeletal health[S] Claude Sonnet 4.6 — synthesized from aggregate training data
subcutaneous injection20 mcgonce daily (morning)post-menopausal women or men with low bone density stacking teriparatide with bisphosphonates or denosumab as follow-on therapy[S] Claude Sonnet 4.6 — synthesized from aggregate training data
subcutaneous injection20 mcgonce dailymale bodybuilders or strength athletes using teriparatide off-label for tendon and ligament repair alongside other peptides (e.g. BPC-157, TB-500)[S] Claude Sonnet 4.6 — synthesized from aggregate training data

Tier key: Research = PMID-cited study · [C] = scraped community source · [S] = model-synthesized from aggregate community reports (softer evidence). How we source.

References

  1. [1] PMID 26902094 — Teriparatide increases bone formation more than resorption; anti-fracture efficacy appears to increase with longer duration; full 24-month course recommended.
  2. [2] PMID 32282692 — Meta-analysis of 14 RCTs: teriparatide associated with lower total vertebral fractures (RR 0.55, 95% CI 0.40–0.77) and nonvertebral fractures (RR 0.65, 95% CI 0
  3. [3] PMID 30890377 — Teriparatide associated with reduced vertebral fracture risk (RR 0.57, 95% CI 0.35–0.93) and increased lumbar spine BMD at 6, 12, 18 months vs. bisphosphonates.
  4. [4] PMID 38064598 — Teriparatide decreased clinical vertebral fractures (OR 1.97) and new vertebral fractures (OR 2.44) compared with bisphosphonates in postmenopausal osteoporosis
  5. [5] PMID 35900607 — Generic teriparatide 20 µg sc daily non-inferior to alendronate 70 mg weekly for lumbar spine BMD change at 48 weeks in Chinese postmenopausal women; AEs more c
  6. [6] PMID 36424580 — 10-year follow-up after ~18-month teriparatide treatment: fracture prevalence fell from 100% to 35% (p<0.0001), to levels similar to general population; BMD inc
  7. [7] PMID 37349750 — Teriparatide superior to bisphosphonates for lumbar vertebral BMD (MD 3.98%, p<0.00001), hip BMD (MD 2.39%), and vertebral fracture prevention in GIOP patients.
  8. [8] PMID 28653616 — In GIO subgroup, teriparatide showed larger BMD increases at lumbar spine, total hip, and femoral neck vs. bisphosphonates; GIO patients less likely to suffer v
  9. [9] PMID 36335582 — In premenopausal women with idiopathic osteoporosis, sequential teriparatide (20 mcg daily for up to 24 months) then denosumab (60 mg q6M for 24 months) signifi
  10. [10] PMID 34490946 — Real-world Medicare data: median teriparatide use 7.2 months; only 40.8% of users switched to antiresorptive agents after discontinuation; suboptimal persistenc
  11. [11] PMID 40119935 — Sequential therapy following once-weekly and daily teriparatide is recommended in osteoporosis guidelines for very high fracture risk patients.
  12. [12] PMID 26144908 — Switching from teriparatide to denosumab: spine BMD increased 18.3% at 48 months; switching from denosumab to teriparatide resulted in transient or progressive
  13. [13] PMID 24517156 — 24-month combined teriparatide (20 µg daily) + denosumab (60 mg q6M) increased lumbar spine BMD 12.9%, femoral neck 6.8%, total hip 6.3% — significantly more th
  14. [14] PMID 32728969 — Meta-analysis of 12 studies (771 patients): teriparatide associated with significantly higher lumbar fusion rates (OR 2.15), reduced vertebral fractures (OR 0.1
  15. [15] PMID 33030619 — 19 studies: bisphosphonates had higher fusion rate (ES 83%) vs. teriparatide (ES 71%), non-significant difference; teriparatide associated with lower (non-signi
  16. [16] PMID 27923758 — Preclinical and early clinical studies show teriparatide increases spinal fusion rates and decreases hardware loosening in postmenopausal osteoporosis.
  17. [17] PMID 40100350 — Perioperative teriparatide significantly reduced PJF incidence vs. denosumab (3.4% vs. 22.2%, p=0.034) and improved postoperative back pain VAS and EQ-5D in ost
  18. [18] PMID 35797582 — 4-month preoperative teriparatide was cost-effective in osteopenic ASD surgery patients, favored in 82% of model iterations with negative incremental cost utili
  19. [19] PMID 40461584 — 12-week daily teriparatide after pertrochanteric fracture fixation significantly shortened mean radiographic union time (7.44 vs. 10.56 weeks, p=0.0083); no sig
  20. [20] PMID 37529188 — Weekly teriparatide improved RUSH scores at 3 and 6 months post-hip fracture surgery and increased lumbar BMD >7% at 1 year.
  21. [21] PMID 32904518 — Meta-analysis: teriparatide reduced time to union (WMD -1.95 months, p=0.003) but did not improve fracture union rate at 3 or 6 months, complications, mortality
  22. [22] PMID 27997614 — Significant improvement in functional outcomes post-fracture but no significant effect on radiographic healing time, fracture healing rate, or pain reduction; n
  23. [23] PMID 25363308 — Animal and limited human trial data suggest a role for teriparatide in improving fracture healing in selected patients; more clinical trial data needed.
  24. [24] PMID 29085957 — Trend for superior healing with immediate vs. delayed teriparatide therapy for bisphosphonate-associated AFF; results require caution given small sample.
  25. [25] PMID 38907093 — Retrospective study (n=59): no significant difference in time-to-bone union between teriparatide and non-teriparatide groups in complete AFF (5.8 vs. 5.5 months
  26. [26] PMID 37695713 — Clinical studies showed beneficial effects of intermittent rhPTH administration in management of MRONJ; short-term teriparatide may be worthwhile in therapy-res
  27. [27] PMID 31429640 — Once-weekly teriparatide without surgical intervention successfully treated MRONJ around a dental implant in an 85-year-old woman.
  28. [28] PMID 34984624 — Subcutaneous infusion via Omnipod pump (mean dose 23–32 mcg/day) normalized calcemia in 2 adults with refractory postsurgical hypoparathyroidism after failure o
  29. [29] PMID 42501079 — Teriparatide maintains serum calcium and significantly lowers serum phosphate (WMD -0.28) vs. conventional therapy in children with hypoparathyroidism; growth a
  30. [30] PMID 36609338 — In vivo studies: PTH(1-34) slowed OA progression by alleviating cartilage degeneration and subchondral bone remodeling; exhibited analgesic and anti-inflammator
  31. [31] PMID 36537662 — In DMM mouse model, teriparatide prevented synovitis and cartilage degradation by suppressing TNF-α–mediated MMP-13 overexpression.
  32. [32] PMID 27374026 — Teriparatide 20 µg/day sc up to 24 months: reduction in nonvertebral fracture incidence, BMD increases, and back pain decrease were similar in T2D and non-diabe
  33. [33] PMID 36522387 — In vitro Mtb-infected MG-63 cell model: teriparatide did not affect MIC of isoniazid/rifampin or anti-TB efficacy; promoted osteoblastic function (ALP-positive
  34. [34] PMID 35220030 — Rat MCAO model: teriparatide promoted angiogenesis via AC/PKA/Ang-1, reduced infarct size, inhibited oxidative stress and neuroinflammation, and protected blood
  35. [35] PMID 41421791 — PPSA-based nano-polymersomes showed 72.2% drug entrapment, strong hydroxyapatite affinity (64.86%), and improved bone regeneration vs. free PTH1-34 in OVX rat m
  36. [36] PMID 40500389 — 20 mcg subcutaneously daily (standard dose) subcutaneous injection (human)
  37. [37] PMID 35893098 — 20 mcg daily subcutaneous injection (human)
  38. [38] PMID 55819 — 20 μg subcutaneously daily subcutaneous injection (human)
  39. [39] PMID 25138261 — 20 µg subcutaneously daily subcutaneous injection (human)
  40. [40] PMID 29996965 — Not specified; lifetime maximum 24 months stated for US indication subcutaneous injection (human)
  41. [41] PMID 36371341 — 100 ng/mL in vitro cell culture (in_vitro)
  42. [42] PMID 34224692 — in-prose reference