Library / Endocrine & Growth / Teriparatide
Evidence: Approved useFDA-approved (Forteo and others)Hormones & bone

Teriparatide

Recombinant PTH(1–34), the active first 34 amino acids of parathyroid hormone.

34Amino acids
~4,117.8Daltons
C₁₈₁H₂₉₁N₅₅O₅₁S₂Formula
2002Research period
TeriparatideIllustrative conformer; drag to rotate.
CNO

Overview

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In plain language

Teriparatide (brand name Forteo, and others) is an FDA-approved medicine for osteoporosis. It is the first 34 amino acids of parathyroid hormone, the body's main controller of blood calcium.

Most osteoporosis medicines slow bone breakdown. Teriparatide is different: a small daily injection under the skin actually builds new bone and lowers the risk of fractures. Side effects can include dizziness and leg cramps.

Molecular identity

Amino acids
34
Molecular weight
~4,117.8 Da
Formula
C₁₈₁H₂₉₁N₅₅O₅₁S₂
Sequence
SVSEIQLMHNLGKHLNSMERVEWLRKKLQDVHNF

Sequence map

HydrophobicPolarPositiveNegativeGly / Pro

Hydropathy

Kyte–Doolittle score per residue. Positive values are water-repelling.

Form clarification: Free peptide identical to human PTH(1–34). Molecular weight is a reference value, not a certificate of analysis.

Origin and history

Teriparatide is the first 34 amino acids of parathyroid hormone, which carry its activity. Given in short daily pulses, it builds bone instead of breaking it down.

A 2001 trial in the New England Journal of Medicine showed large drops in spine fractures. Eli Lilly’s Forteo was approved in 2002. Rat studies had shown bone tumors, so it carried a boxed warning that was removed in 2020 after years of human safety data.

Key people

  • Robert NeerLead author of the 2001 fracture trial

Timeline

  1. 2001

    Pivotal fracture trial published

  2. 2002

    FDA approves Forteo

  3. 2020

    Boxed warning removed

See every peptide on one history timeline.

Human evidence

PreclinicalEarly humanControlled trialsApproved use

Randomized trials showed fewer vertebral and nonvertebral fractures.

Registration and enrollment are not proof of benefit; check study results directly.

Explore original publications and distinguish preclinical findings from controlled human evidence.

Safety and regulatory status

See every compound on the regulatory tracker.

FDA-approved. A boxed warning about bone cancer (based on rat studies) was removed from the label in 2020.

This profile is educational and does not provide treatment, dosing or sourcing guidance.

Sources

  1. PubMed literature search: Teriparatide
  2. PubChem compound search: Teriparatide
  3. DailyMed (FDA label search): Teriparatide
  4. Neer et al. 2001, NEJM
  5. ClinicalTrials.gov search: Teriparatide
Cite this page

Hernandez Gener, E. (2026, November 7). Teriparatide: molecular data, research history and evidence. VALREXA Biosciences. https://valrexa.com/peptides/teriparatide.html

APA style · Last reviewed November 7, 2026 · Our editorial standards

Last reviewed November 7, 2026. Trial and regulatory status can change; confirm in the linked registries. This profile is educational and is not medical advice, a treatment recommendation, or dosing or sourcing guidance. Report an error · Corrections policy

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