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Abaloparatide

Also called Tymlos, BA058

InjectableEvidence AEvery day
Half-life
1.7hours
Typical vial
1 / 2mg
Research amounts
80–80mcg

per administration

Common schedule
Every day
Tested in people

A human trial worked out how much to take and how often, so a dosing schedule is shown.

Licensed as a medicine in the US and EU.

Quick start

Abaloparatide at a glance — the figures, plus how it's commonly run. Reference only, not medical advice.

Typical dose
80–80 mcg per administration
How often
Every day
Where
Subcutaneous — abdomen, thigh, or upper arm Sites and rotation
Time to steady level
~9 hours — about five half-lives
Storage
Dry vial kept cold and dark; a mixed vial in the fridge at 2–8 °C. Details

A research and community reference, not medical advice. Figures are descriptive, vary between sources, and are not a recommendation for use.

Work out your draw

These numbers are a starting point — change any of them.

Vial label

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Published research contexts for Abaloparatide describe 8080 mcg per administration. Descriptive only, not a recommendation.

A synthetic analog of parathyroid-hormone-related protein, PTHrP(1–34), licensed as a medicine in the US and EU. The ACTIVE study (Miller, JAMA 2016) used a single amount, 80 mcg subcutaneously once daily.

Dosing schedule

How Abaloparatide is commonly stepped up, for reference only.

These are commonly-discussed research protocols shared for educational reference. This is not medical advice and is not a substitute for guidance from a qualified professional.

PhaseAmountFrequencyRoute
StandardThe single amount used across the ACTIVE study.80 mcgOnce dailySubQ

Modelled level — every day

1× is the peak after a single dose.

Steady-state peak
0.99× single dose

Read off the modelled curve, not an even-interval formula

Time to steady state
9hours

About five half-lives

Administrations
7/ week

Where these numbers come from

  • Miller PD et al., JAMA 2016;316:722 (ACTIVE)Daily subcutaneous 80 mcg versus placebo and open-label teriparatide over 18 months, with new-fracture and bone-density endpoints in postmenopausal osteoporosis research.

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