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Drug

Etelcalcetide hydrochloride

Approved medicine
ResearchOngoing clinical research

Also known as Parsabiv, etelcalcetide (as hydrochloride), etelcalcetide HCl.

1
Regulatory events
Latest activity
beta

Recent clinical, regulatory, research and industry developments relating to this drug.

Profile

Identifiers & mechanism

Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.

Canonical name
Etelcalcetide hydrochloride
Aliases & brands
Parsabivetelcalcetide (as hydrochloride)etelcalcetide HCl
RxNorm CUI
1876122
Regulatory jurisdictions
ema

Regulatory timeline

1 event

The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.

Earliest approval
2016-11-11
Latest approval
2016-11-11
Authorities
EMA
Total events
1
emaEuropean Medicines Agency· 1 event
2016-11-11Approval
Approval: Parsabiv (EMA)

Indication: Parsabiv is indicated for the treatment of secondary hyperparathyroidism (SHPT) in adult patients with chronic kidney disease (CKD) on haemodialysis therapy.

Evidence ↗

Contains information from the European Medicines Agency (European Medicines Agency), © EMA, reused under CC BY 4.0.

Clinical trials

1 trials

The current development programme across all trial phases — status mix, phase distribution and the late-stage studies shaping the evidence base.

Development programme
CLINICALTRIALS.GOV · LIVE REGISTRY
1
registered trials across all phases
LATEST COMPLETION 2025
1
Completed
PHASE DISTRIBUTIONn = 1
Phase 21
References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • ClinicalTrials.gov — clinical trials
  • Regulatory event sources are credited in the Regulatory Timeline above.