Etelcalcetide
Calcium-sensing Receptor Agonist — SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS
Also known as: AMG 416, etelcalcetide HCl, etelcalcetide hydrochloride, KAI-4169, parsabiv, velcalcetide, velcalcetide hydrochloride
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Etelcalcetide is an onp drug in the Calcium-sensing Receptor Agonist class catalogued in DrugCentral. It was first approved by the EMA in 2016. Its mechanism of action is classified as Increased Calcium-sensing Receptor Sensitivity. DrugCentral lists 1 molecular target, including CASR. Recorded indications include Secondary hyperparathyroidism.
- Approval status: onp (first approved 2016 by the EMA).
- Drug class: Calcium-sensing Receptor Agonist.
- Mechanism of action: Increased Calcium-sensing Receptor Sensitivity.
- Molecular targets: CASR (1 listed in DrugCentral).
- Indications: Secondary hyperparathyroidism.
- ATC code: H05BX04 (Other anti-parathyroid agents).
- Molecular formula: C38H73N21O10S2; molecular weight 1048.26 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Secondary hyperparathyroidism
Mechanism & targets
| Mechanism of action (MoA) | Increased Calcium-sensing Receptor Sensitivity |
|---|---|
| Established pharmacologic class | Calcium-sensing Receptor Agonist |
Molecular targets (1)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Extracellular calcium-sensing receptor | CASR | agonist | EC50 4.60 |
Regulatory approvals (2)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2017-02-07 | FDA | — | KAI PHARMS INC | |
| 2016-11-11 | EMA | — | Amgen Europe B.V. |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
H05BX04 | SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS › CALCIUM HOMEOSTASIS › ANTI-PARATHYROID AGENTS › Other anti-parathyroid agents |
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Shunt stenosis | 1490.2 |
| Shunt occlusion | 824.3 |
| Underdose | 798.7 |
| Blood parathyroid hormone increased | 726.0 |
| Hypocalcaemia | 442.0 |
| Blood calcium decreased | 401.8 |
| Peripheral arterial occlusive disease | 249.0 |
| Product storage error | 225.9 |
| Blood parathyroid hormone abnormal | 202.4 |
| Angina unstable | 105.9 |
| Shunt infection | 104.6 |
| Blood calcium increased | 102.2 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Etelcalcetide is on its molecule page.
| Molecular formula | C38H73N21O10S2 |
|---|---|
| Molecular weight | 1048.26 g/mol |
| CAS number | 1262780-97-1 |
| InChIKey | ANIAZGVDEUQPRI-ZJQCGQFWSA-N |
| PubChem CID | 71511839 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Etelcalcetide used for?
DrugCentral lists the following indications for Etelcalcetide: Secondary hyperparathyroidism.
How does Etelcalcetide work?
Etelcalcetide is classified as Increased Calcium-sensing Receptor Sensitivity; its molecular targets in DrugCentral include CASR (agonist).
When was Etelcalcetide first approved?
Etelcalcetide was first approved by the EMA in 2016.
What drug class does Etelcalcetide belong to?
Etelcalcetide is in the Calcium-sensing Receptor Agonist class.
What is the chemical formula of Etelcalcetide?
Etelcalcetide has the molecular formula C38H73N21O10S2 and a molecular weight of 1048.26 g/mol.
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Sources
- DrugCentral drug card 5181 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL3545183 — compound record and bioactivity
- PubChem CID 71511839 — chemical identifiers
- DrugBank DB12865 — drug record
- FDA UNII 60ME133FJB — substance identity
- DailyMed: FDA labels for Etelcalcetide — current prescribing information (label search)
- UniProt P41180 (CASR) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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