What is Teriparatide?
Teriparatide is the active piece of the body's own parathyroid hormone (the first 34 amino acids, hence PTH 1-34). It is clinically approved for treating osteoporosis and one of the few agents that actively builds bone rather than just slowing breakdown.
Comparison
Two paths to bone formation via PTH1R
Teriparatide next to abaloparatide, as stated in the TPD lexicon. Tap a card to open its entry.
Simplified: both act on the same receptor, abaloparatide is a derivative of the PTH-related peptide. 8
How it works
The trick is in the timing: continuously elevated parathyroid hormone breaks down bone, while a once-daily short dose stimulates the bone-building cells (osteoblasts) more than the breaking-down ones. Net new bone forms, especially in the spine and hip.
Where it acts
One receptor, several sites of action
Tap a point or a card. Colour = receptor, grey = observed.
- Bone
New vertebral fractures 5 instead of 14 percent, lumbar density +9 percentage points over placebo1
PTH1R - Kidney
Controls reabsorption of calcium and phosphate, more calcium in urine6
PTH1R - Blood
Calcium briefly raised 4 to 6 hours after the dose, above normal in 11 percent of women6
Observed in trials - Circulation
Brief drop in blood pressure on standing in 5 percent of healthy volunteers during the first doses6
Observed in trials
Targets in the ChEMBL database8
Compound CHEMBL525610: one recorded mechanism, Agonist, binds with the same affinity as full parathyroid hormone.
- Gene
- PTH1R
- UniProt
- Q03431
- ChEMBL
- CHEMBL1793
- Action
- Agonist, binds with the same affinity as full parathyroid hormone
What you need
- The teriparatide vial (lyophilized powder).
- Bacteriostatic water, U-100 insulin syringes, alcohol swabs.
- A sterile empty vial for the dilution.
Reconstitution
Teriparatide is dosed in mcg, the standard dose is 20mcg (0.02mg). From a 10mg vial this cannot be measured accurately with a U-100 syringe directly: with 2ml water the vial gives 5mg per ml, so 20mcg would be only 0.004ml, i.e. 0.4 units. That is why it is diluted in two steps:
- Dissolve the 10mg vial in 2ml water. That gives 5mg per ml.
- Transfer 0.1ml of it (10 units, i.e. 0.5mg) into a sterile empty vial.
- Add 2.4ml bacteriostatic water. The empty vial then holds 0.5mg in 2.5ml, i.e. 200mcg per ml.
20mcg is then 0.1ml, i.e. 10 units on the U-100 syringe. One diluted vial lasts for 25 doses. The peptide calculator does not cover the second step, so it shows no dose steps for teriparatide.
Step by step
Dissolving the powder
Four steps, the same for every vial size.
- 1Wipe the cap
Clean the rubber stopper with an alcohol swab.
- 2Add BAC water
Just add it, it does not matter if it hits the powder directly.
- 3Swirl or shake
Until everything has dissolved, both are fine.
- 4Draw up
With the U-100 insulin syringe.
Dosing
Dosing
Dosing, titration and syringe
Loading the dosing information …
- Getting started and stepping up, drawn as a staircase
- Units on the U-100 syringe for every step
- How long one vial lasts
Injection
Subcutaneous into the subcutaneous fat (abdomen or the front and inner side of the thigh). Disinfect the site, pinch a skin fold, insert at 90 degrees (45 degrees with little fat under the skin), rotate sites.
What the research shows
The approval study (Neer, NEJM 2001) showed a marked reduction of new vertebral fractures and an increase in bone density in postmenopausal women with osteoporosis. Teriparatide is thus a well-evidenced, clinically established agent with solid data.
Study results
What the trials measured
Interactive: switch tabs, tap points, show or hide arms. Arms are named relative to each other, no dosing advice.
New fractures in the approval trial1
Share of women with a new fracture, median observation 21 months
The higher dose raised bone density more but did not lower fracture risk further and had side effects more often. The standard dose is therefore the approved one.
Bone density beyond placebo1
Difference from placebo in percentage points, measured by DXA
At the forearm (radius) density fell 2 percentage points more than on placebo with the higher dose.
Fractures after 24 months in severe osteoporosis2
Share with a new fracture, 680 women each, double-blind
Vertebral and clinical fractures differed significantly. For the other fractures the difference was not significant.
Osteoporosis caused by cortisone, 18 months3
428 women and men, teriparatide against alendronate
Other fractures were about equally frequent in both groups. On teriparatide more participants had raised blood calcium at least once.
Research status
Where the research stands
A selection from 182 registry entries, among them 32 in phase 3 and 48 in phase 4. Shown are the approval trial, large comparison trials and studies on new forms. As of 26 Oct 2026. 7
- Preclinical Bone formation and long-term safety in rats
- Phase 1 2 trials, 2 completed
- Phase 2 no registered trial
- Phase 3 5 trials, 5 completed
- Approval for osteoporosis since 2002
Show all 6 phase 3 and 4 trials on a timelineHide timeline
NCT00670501 · 1,637 participants, started Aug 1996, primary endpoint reached Apr 1999.
Registry entry ↗ · Results: Neer et al., New England Journal of Medicine, 2001
NCT00051558 · 428 participants, started Nov 2002, primary endpoint reached Jul 2006.
Registry entry ↗ · Results: Saag et al., New England Journal of Medicine, 2007
NCT00343252 · 712 participants, started Jun 2006, primary endpoint reached Jun 2009.
Registry entry ↗ · Results not yet in PubMed
NCT00433160 · 207 participants, started Jan 2007, primary endpoint reached Sept 2008.
Registry entry ↗ · Results not yet in PubMed
NCT01473589 · 122 participants, started Feb 2012, primary endpoint reached Dec 2013.
Registry entry ↗ · Results not yet in PubMed
VERO · NCT01709110 · 1,366 participants, started Oct 2012, primary endpoint reached Jul 2016.
Registry entry ↗ · Results: Kendler et al., The Lancet, 2018
Bar: start to primary endpoint (planned for running trials). Green = completed, blue = progress until 26 Oct 2026. Phase 1: 2 trials on safety and pharmacokinetics, not shown as bars.
Side effects
- Dizziness, leg cramps, nausea, especially at the start.
- Temporary rise in blood calcium.
- Local reactions at the injection site.
Tolerability
Frequency in the two main trials
Out of 100 participants per group, how many had the event in the two main trials in women and men.
| Event | Placebo | Teriparatide |
|---|---|---|
| Joint pain6 | 8% | 10% |
| Nausea6 | 7% | 9% |
| Dizziness6 | 5% | 8% |
| Leg cramps6 | 1% | 3% |
| Briefly raised calcium (women)6 | 2% | 11% |
Calcium rose briefly 4 to 6 hours after the dose and was back to baseline after 16 hours. In healthy volunteers 5 percent had brief dizziness on standing during the first doses.6
Storage
Delicate: keep refrigerated throughout (2 to 8 degrees), do not freeze and protect from light. Once mixed, it keeps for at least 4 to 6 months in the fridge (2 to 8 °C).
Shelf life
How long it keeps
Delicate: keep refrigerated even before mixing, do not freeze.
Keeps for at least 4 to 6 months.
- Keep it dark
- Dissolved: 2 to 8 degrees
- Note the mixing date on the vial