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Abaloparatide (Tymlos)_Dosage, benefits & legal status

Also known as Tymlos, BA058

Published August 24, 2026 · Updated October 5, 2026

A bone-building drug that completes the family around teriparatide.

Bone densityPTHrP analogFDA-approved
DoseSet by the label
FrequencyOnce daily
RouteUnder the skin (subcutaneous)
StatusFDA-approved
CycledSet by the prescription

Common vial size is what vendors typically sell, not a recommendation. Enter your own vial in the calculator.

See how this dose compares across the library →

01

What is Abaloparatide (Tymlos)?

Plain language first. The technical label stays, but it never stands alone.

Overview

A daily injection that builds new bone rather than just slowing its loss. It copies a different hormone from teriparatide and does much the same job.

The technical version

Abaloparatide, a synthetic analog of parathyroid hormone-related protein (PTHrP 1-34), acting as an anabolic agent at the PTH1 receptor. FDA-approved 28 April 2017 as Tymlos for postmenopausal women with osteoporosis at high risk of fracture, with later expansion to men. Approval included enhanced pharmacovigilance for osteosarcoma reports, scheduled for reassessment fifteen years after approval.

What it's used for

A daily injection for osteoporosis in people at high risk of fracture.

02

How does Abaloparatide (Tymlos) work?

What it does in the body, and where.

Abaloparatide sits next to teriparatide in this library, and the difference between them is which hormone each copies.

  1. 01
    Anabolic, not antiresorptive
    Most osteoporosis drugs slow the breakdown of bone. Abaloparatide and teriparatide stimulate new bone formation, which is a different and more demanding thing to achieve.
  2. 02
    It copies PTHrP rather than PTH
    Teriparatide is parathyroid hormone fragment 1-34. Abaloparatide is an analog of parathyroid hormone-related protein. Both act at the same receptor with different binding behavior.
  3. 03
    Intermittent dosing is the trick
    Continuous parathyroid hormone signaling breaks bone down. A single daily pulse builds it up. The entire drug class depends on that distinction, which is why the dosing schedule is not negotiable.
  4. 04
    The osteosarcoma question shaped the label
    Rodent studies in this drug class raised bone cancer concerns, and the FDA required enhanced pharmacovigilance for reports of osteosarcoma with abaloparatide, to be reassessed fifteen years after approval.
03

What else is it used for?

Each use below carries its own evidence level. Approved means regulators have cleared it for that purpose. Investigational means it is in trials. Early research means it is being studied and is not established.

  • Postmenopausal osteoporosis at high risk of fractureFDA-approved
  • Osteoporosis in men at high risk of fractureFDA-approved
  • General bone health or fracture healing outside those settingsnone

The published record

Research index

428

Papers and trials about Abaloparatide (Tymlos)

263 papers tagged human · 124 not reviews or lab · 36 clinical trial publications

25 registered trials · 11 with posted results

Furthest stage reached: Approved in the US

Compare this against the whole library →

In animals84
In the lab4
Reviews142
Senior author shareSpread across many groups

Evidence summary

Counted from Europe PMC indexing, not read by a person; a human tag can land on reviews, commentary or lab papers; clinical trial publications is the narrower count. 400 papers and 25 trials indexed in detail.

Abaloparatide (Tymlos) vial rendering
Compound field notes

At a glance

Four things to know about Abaloparatide (Tymlos)

01

Evidence

FDA-approved

02

Category

Healing and recovery

03

Common vial

Varies

04

Half-life

1 to 2 hours

04

How much, and do you cycle it?

The range, and whether you take breaks.

Set by the label, once daily. Set by the prescription FDA label

This is a prescription drug. Duration and schedule are set by the label and the prescriber, not by a cycling convention.

Compare this against the whole library →

05

How long does it stay in the body?

The half-life, and where the figure comes from.

1 to 2 hoursFDA label

The figure changed between label versions. The original 2017 Tymlos label states a mean half-life of 1.7 hours. The 2024 revision states approximately 1 hour. Both are the same drug and the same section of the label, so a figure quoted without its label year is incomplete.

Source: Tymlos label section 12.3. The 2017 label gives 1.7 hours, the 2024 revision gives about 1 hour.

You can compare this against the whole library to see where it sits.

06

How do I dose and price it?

Enter your vial and your dose. Pick a mix. We show the draw and the cost.

The vial holds a fixed amount of drug. Adding more water does not make more drug, it just spreads it thinner, so you draw a bigger number on the syringe for the same dose.

Your vial size (mg)
Printed on the vial.
What you paid per vial
$
Used for cost per dose only.
Your dose (mcg)
Commonly referenced dose: 80 mcgFDA label

Choose your mix

your own mL
units · —
Enter your own volume

Measuring the water1 mL = one full 100-unit syringe.

YOUR DRAW1.6 / 100 units
1.6 units is a very small line to read, so a small slip is a large error. A larger water volume above spreads the same dose across more units.
07

How do you store it?

Before mixing, and after.

Dry powder in the freezer or fridge. Once mixed, fridge, and use within about a month.

Unmixed lyophilized Abaloparatide (Tymlos) keeps for a long time cold. Once you add water the clock starts: most reconstituted vials hold up for roughly 28 to 30 days at fridge temperature. Keep it out of light, and do not freeze it after mixing.

08

What are the side effects and cautions?

Known cautions and warnings for this compound.

Solubility, computed: 41% charged residues, 38% hydrophobic. Water usually sufficient.

A first-pass rule from peptide manufacturers' guidance. It does not account for disulfide bridges, salt form or how the powder was dried, and it predicts what should be easy rather than what will happen in your vial.

Who should avoid it

Check these before anything else.
  • Pregnancy or breastfeeding
  • Any condition raising the baseline risk of osteosarcoma, including Paget's disease of bone and prior radiation to the skeleton
  • High blood calcium
  • Use outside a prescription, where no label governs the dose or the treatment duration

Stop and get help

These are emergencies. Seek care.
  • Fainting, or dizziness severe enough to cause a fall
  • Signs of high blood calcium, including persistent nausea, vomiting, constipation or confusion
  • Signs of an allergic reaction, including facial or throat swelling or trouble breathing
  • New or persistent bone pain

Common effects

Expected, and usually mild.
  • Dizziness and light-headedness, particularly after the first doses
  • Palpitations
  • Nausea
  • Headache
  • Injection site reactions
  • Raised blood calcium

Where this page says nothing is established, that means nobody has studied it, not that a compound is safe.

09

Is Abaloparatide (Tymlos) approved?

And where the numbers on this page come from.

Yes. Abaloparatide (Tymlos) is FDA approved and available on prescription in the United States.

  • Approval status
    FDA-approved
  • Route
    Under the skin (subcutaneous)
  • Checked
    24 August 2026
  • Dose
    From the drug label. The manufacturer tested this range and a regulator reviewed it.
  • Vial size
    From what vendors typically list; not a recommendation.
  • Sources
    None traced yet.

What has happened recently

FDA-approved 28 April 2017 as Tymlos for postmenopausal osteoporosis at high risk of fracture, later expanded to men with osteoporosis. Prescription only. The approval included enhanced pharmacovigilance for osteosarcoma reports.

Guides for this compound

Sources

No primary source has been traced for this compound yet. Treat everything on this page as unverified until one is. How we grade evidence

Beyond these, 425 records are indexed. Browse the records