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Peptide approval and research checker

Enter a peptide or brand name. See its status, research in people, and product limits.

Uses saved U.S. Food and Drug Administration (FDA) records and research summaries. For current status, check the official FDA record. This tool does not give medical advice or verify a product.

Review · United States

Abaloparatide

Reviewed on

Read the full Abaloparatide review

Approval and product status

An FDA-approved product exists for defined osteoporosis populations

The study result belongs to the named prescription product, not every similar product or use. Tymlos is a product-specific prescription medicine. Trial findings do not validate unapproved PTHrP analogues or general performance use.

What was measured in people?

Health results · Strong
The ACTIVE phase 3 trial supports fracture-risk reduction in postmenopausal women with osteoporosis.
Body changes · Strong
Approved labeling characterizes PTH1-receptor activity, exposure, and bone-turnover effects.

A change in a hormone or body signal does not by itself prove a health benefit.

Important limits

This tool is not an independent medical review. It does not recommend treatment.

This prescription osteoporosis medicine has product-specific warnings and limits on use. No dose, injection, or performance guidance is provided.

Still unknown: The result does not establish that it is better than every osteoporosis medicine, improves healthy people, or heals every new injury better.

This record cannot check a package, seller, batch, or personal treatment. It does not provide sport clearance.

Products in this review

These are selected records, not every product or form.

Tymlos

Ingredients and form
Injection pen
How it enters the body
Under the skin (subcutaneous)
Use and people covered
Osteoporosis uses in the high-fracture-risk populations defined in the product label.

Published label: 2025 label

Read the published Tymlos FDA label (PDF)

What the research shows

The ACTIVE study compared abaloparatide with placebo or open-label teriparatide in postmenopausal women with osteoporosis. Abaloparatide reduced new spine and non-spine fractures versus placebo over 18 months.

Read all Abaloparatide fact checks

Sources used in this review

A source may support some statements, not all of them. Use the links above or this review to see what each source supports.

Show 3 sources
  1. TYMLOS (abaloparatide) prescribing information

    U.S. Food and Drug Administration · Drug label · 2025

    Source accessed

  2. Abaloparatide vs placebo on new vertebral fractures: ACTIVE

    PubMed · JAMA · Randomized trial · 2016

    Source accessed

  3. Drug approvals and databases

    U.S. Food and Drug Administration · Regulatory · 2026

    Source accessed

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Dataset version 2026-09-11.1. This endpoint grants no additional reuse license. Keep the verdict, scope, evidence basis, review date, and source links together. Do not present a record as medical advice or medical review.

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What this checker shows

Why approval and research can differ

Approval applies to an exact product and use. Research may cover a different form, group of people, or outcome.

This tool keeps those questions separate. There is no safety score or treatment ranking.

Learn what FDA approval covers

Check the sources.

Results use this site’s reviews. They show source dates, product labels, study limits, and links to the original records.

The checker gives no answer for an unknown name. A listed entry without a full review stays marked as incomplete.

Read the research standard

Coverage and review dates

34 reviewed records and 20 listed names. This is not a complete list of peptides or approved medicines.

Reviews range from July 23, 2026 to October 12, 2026.

The site editor reviews the sources. This is not an independent medical review. Use the current official record to check for later changes.

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