Approved / ClinicalFDA-approvedApprovedUpdated 2026-04-24

Peptide reference file

Abaloparatide

Trending #39 in Approved8.4k searches/moProven

Abaloparatide is a PTHrP analog used in approved bone-health contexts and sits beside teriparatide in osteoanabolic peptide medicine.

Current readout: approved evidence, fda-approved status, approved approval state, human evidence appears in the current trail, registered trials are linked, and 3 linked sources in the seed trail.

PubChem CID 76943386 | 393 PubMed results | 23 trial records | 1 DailyMed label | 1 Drugs@FDA application

Abaloparatide is mostly discussed because it helps show how short peptide analogs can become highly targeted endocrine medicines.

The public claim is straightforward: It helps show how short peptide analogs can become highly targeted endocrine medicines. Approved osteoanabolic peptide analog with direct human evidence.

In plain language, abaloparatide is a PTHrP analog used in approved bone-health contexts and sits beside teriparatide in osteoanabolic peptide medicine.

ApprovedFDA-approved
PTH receptorBone formationOsteoanabolic

Aliases: Tymlos, PTHrP analog

SpecimenAbaloparatide specimen
CCCCHHHHHHHNO
Formula
C174H300N56O49
Mass
3961
Evidence
Approved
Elements
4

Most commonly discussed in relation to PTH receptor, Bone formation, Osteoanabolic.

What Abaloparatide is

Abaloparatide is a PTHrP analog used in approved bone-health contexts and sits beside teriparatide in osteoanabolic peptide medicine.

Abaloparatide is grouped under Approved / Clinical on PeptideFactCheck because it helps show how short peptide analogs can become highly targeted endocrine medicines.

The useful starting point is to separate the molecule itself from the internet story around it. It helps show how short peptide analogs can become highly targeted endocrine medicines.

Why people keep looking it up

It helps show how short peptide analogs can become highly targeted endocrine medicines.

Abaloparatide is a PTHrP analog used in approved bone-health contexts and sits beside teriparatide in osteoanabolic peptide medicine.

Abaloparatide tends to stay in the conversation because it touches a familiar public theme: pth receptor, bone formation, and osteoanabolic. That makes it easy for the claim to travel faster than the evidence.

What the evidence can support right now

Approved osteoanabolic peptide analog with direct human evidence.

Human trials and labeling support specific approved uses.

Mechanism aligns with PTH receptor pharmacology and bone-remodeling biology.

Why this page carries the current tier: Approved osteoanabolic peptide analog with direct human evidence.

The current seed trail for Abaloparatide is pulling from 1 labels source, 1 regulatory source, and 1 literature source.

Safety, limits, and regulatory context

Bone-active endocrine drugs need label-specific reading rather than generic anabolic language.

FDA-approved abaloparatide products exist for specific indications.

Editorial boundary: PeptideFactCheck does not publish dosing, cycling, sourcing, injection, or administration instructions for Abaloparatide. The job here is to explain the public claim, the mechanism story, the evidence strength, and the current limits.

Molecular and identifier data

The current PubChem match for Abaloparatide is CID 76943386. That gives the page a source-backed chemistry record rather than a placeholder identifier block.

PubChem CID
76943386
Formula
C174H300N56O49
Molecular weight
3961
InChIKey
BVISQZFBLRSESR-XSCWXTNMSA-N

Matched synonyms include Abaloparatide, Tymlos, BA058, 247062-33-5, BIM-44058, AVK0I6HY2U, abaloparatida, abaloparatidum.

Open PubChem record

Clinical trial snapshot

The current ClinicalTrials.gov intervention query for Abaloparatide returns 23 study records. This does not prove efficacy by itself, but it does show whether the peptide is showing up in a formal trial registry rather than only in forums or vendor copy.

Literature snapshot

The current PubMed query for Abaloparatide returns 393 results. The articles below are a quick literature surface so the page shows actual papers instead of only generic evidence labels.

Label and regulatory records

For approved or clinically developed peptides, the page now pulls in official labeling and FDA-facing records where they exist. That makes the regulatory section materially more useful than a generic approved or not-approved tag.

Brand names
Tymlos
Generic names
ABALOPARATIDE
Routes
SUBCUTANEOUS
Application numbers
NDA208743

Indications and usage. 1 INDICATIONS AND USAGE TYMLOS is a human parathyroid hormone related peptide [PTHrP(1-34)] analog indicated for the: Treatment of postmenopausal women with osteoporosis at high risk for fracture or patients who have failed or are intolerant to other available osteoporosis therapy. ( 1.1 ) Treatment to increase bone density in men with osteoporosis at high risk for fracture or patients who have failed or are intoler...

Warnings and cautions. 5 WARNINGS AND PRECAUTIONS Osteosarcoma: Avoid use in patients with increased risk of osteosarcoma including patients with open epiphyses, metabolic bone diseases including Paget's disease, bone metastases or history of skeletal malignancies, prior external beam or implant radiation therapy involving the skeleton, and hereditary disorders predisposing to osteosarcoma. ( 5.1 ) Orthostatic Hypotension: Instruct patien...

Contraindications. 4 CONTRAINDICATIONS TYMLOS is contraindicated in patients with a history of systemic hypersensitivity to abaloparatide or to any component of the product formulation. Reactions have included anaphylaxis, dyspnea, and urticaria [see Adverse Reactions ( 6.2 )] . Known hypersensitivity to TYMLOS. ( 4 )

Source trail

Each linked source is shown directly so the page can be audited. The page now combines its editorial seed trail with automated official-source enrichment generated on 2026-04-24 from PubChem, ClinicalTrials.gov, PubMed, DailyMed, openFDA label, and Drugs@FDA.

Safety noteThis content is educational only and does not replace medical advice. Peptide use may carry risks and should be discussed with a qualified medical professional.