Back to discover
Drug

Paricalcitol

Approved · FDA
ClassVitamin D receptor agonistEmerging researchLate-stage developmentSteady momentum

Also known as 19-Nor-1alpha,25-dihydroxyvitamin D2, Zemplar.

4
Research papers
2
Active clinical trials
Vitamin D3 receptor
Primary target
2
Regulatory events
Latest activity
beta

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

A PiLot ClinicaL TrIal of ParicAlcitol for ChroNiC PancrEatitis

Clinical trial2026-06-01Primary completion · ClinicalTrials.gov

Approval: PARICALCITOL (NDA205917)

Regulatory2014-11-18FDA

Profile

Identifiers & mechanism

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

Canonical name
Paricalcitol
Aliases & brands
19-Nor-1alpha,25-dihydroxyvitamin D2Zemplar
RxNorm CUI
73710
ChEMBL ID
CHEMBL1200622
ATC codes
H05BX02
UNII
6702D36OG5
Primary mechanism
Vitamin D receptor agonist
Regulatory jurisdictions
fda

Pharmacology & targets

1 target

Known molecular targets and mechanisms supported by curated pharmacology databases.

Vitamin D3 receptor
VDR · P11473
AGONISTVitamin D receptor agonist

Regulatory timeline

2 events

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
2014-11-18
Latest approval
2014-11-18
Authorities
FDA
Total events
2
fdaU.S. Food and Drug Administration· 2 events
2026-06-17Label change
Label change: PARICALCITOL (NDA205917)
Evidence ↗
2014-11-18Approval
Approval: PARICALCITOL (NDA205917)
Evidence ↗

Data from the U.S. Food and Drug Administration (U.S. Food and Drug Administration), public domain (CC0).

Clinical trials

89 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
89
registered trials across all phases
LATEST COMPLETION 2025
2
Active studies
2
Recruiting
57
Late-stage (III+)
67
Completed
20
Discontinued
PHASE DISTRIBUTIONn = 89
Early Phase 12Phase 110Phase 220Phase 2 / 31Phase 320Phase 426Phase N / A10

Late-stage studies

Phase III+ trials still open or recently active — where late-stage evidence is being generated.

Recent completions

Trials that read out recently, adding to the completed evidence base.

Research activity

4 papers

Key research shaping understanding of this drug, combining the latest publications with the most influential evidence.

Publications over time
20082025
Major research themes7
Antibodies, Monoclonal, Humanized1Antineoplastic Combined Chemotherapy Protocols1Carcinoma, Pancreatic Ductal1Cytoreduction Surgical Procedures1Ergocalciferols1Pancreatic Neoplasms1Renal Dialysis1
Journals, researchers & institutions
Top journals
  • Hypertension (Dallas, Tex. : 1979)1
  • Kidney international1
  • Pediatric nephrology (Berlin, Germany)1
  • The oncologist1
Leading researchers
  • Agarwal R1
  • Alborzi P1
  • Alistar A1
  • Ariceta G1
  • Barrett MT1
  • Becerra C1
  • Bekele DM1
  • Bills JE1
Leading institutions
free-text, unnormalised
  • Atlantic Medical Group-Oncology Morristown Medical Center1
  • Center for Pediatric Nephrology1
  • Children's Mercy Hospital1
  • City of Hope National Medical Center1
  • Department of Paediatric Nephrology and NIHR/Wellcome Trust Clinical Research Facility1
  • Division of Nephrology and Kidney Research Institute1

Related drugs

1 matches

Drugs sharing diseases, protein targets and literature with this one. Ranked by graph evidence (shared targets + diseases weighted above co-mentions).

Studied across 3 of the same disease areas as Paricalcitol in the shared literature.

3 shared diseases1 shared paper
References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • ChEMBL (EMBL-EBI) & UniProt — pharmacology and targets
  • Europe PMC — research literature
  • ClinicalTrials.gov — clinical trials
  • Regulatory event sources are credited in the Regulatory Timeline above.