Paricalcitol

Paricalcitol

Clinical data
Trade names	Zemplar
Other names	(1R,3S)-5-[2-[(1R,3aR,7aS)-1-[(2R,5S)-6-hydroxy-5,6-dimethyl-3E-hepten-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-cyclohexane-1,3-diol
AHFS/Drugs.com	Monograph
MedlinePlus	a682335
Pregnancy category	AU: C
Routes of administration	Oral, Intravenous
ATC code	H05BX02 (WHO)
Legal status
Legal status	AU: S4 (Prescription only) CA: ℞-only UK: POM (Prescription only) US: ℞-only
Pharmacokinetic data
Bioavailability	72%[1]
Protein binding	99.8%[1]
Metabolism	Hepatic[1]
Elimination half-life	14-20 hours[1]
Excretion	Faeces (74%), urine (16%)[1]
Identifiers
IUPAC name (1R,3R,7E,17β)-17-[(1R,2E,4S)-5-hydroxy-1,4,5-trimethylhex-2-en-1-yl]-9,10-secoestra-5,7-diene-1,3-diol
CAS Number	131918-61-1 Y
PubChem CID	5281104
IUPHAR/BPS	2791
DrugBank	DB00910 N
ChemSpider	4444552 Y
UNII	6702D36OG5
KEGG	D00930 N
ChEBI	CHEBI:7931 N
ChEMBL	ChEMBL1200622 Y
CompTox Dashboard (EPA)	DTXSID4048640
ECHA InfoCard	100.184.862
Chemical and physical data
Formula	C27H44O3
Molar mass	416.646 g·mol−1
InChI InChI=1S/C27H44O3/c1-18(8-9-19(2)26(3,4)30)24-12-13-25-21(7-6-14-27(24,25)5)11-10-20-15-22(28)17-23(29)16-20/h8-11,18-19,22-25,28-30H,6-7,12-17H2,1-5H3/b9-8+,21-11+/t18-,19+,22-,23-,24-,25+,27-/m1/s1 Y Key:BPKAHTKRCLCHEA-UBFJEZKGSA-N Y
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Paricalcitol (chemically it is 19-nor-1,25-(OH)₂-vitamin D₂. Marketed by Abbott Laboratories under the trade name Zemplar) is a drug used for the prevention and treatment of secondary hyperparathyroidism (excessive secretion of parathyroid hormone) associated with chronic kidney failure. It is an analog of 1,25-dihydroxyergocalciferol, the active form of vitamin D₂ (ergocalciferol).

It was patented in 1989 and approved for medical use in 1998.^[2]

Its primary use in medicine is in the treatment of secondary hyperparathyroidism associated with chronic kidney disease.^[3] However a 2016 systematic review did not find evidence sufficient to demonstrate an advantage of paricalcitol over non-selective vitamin D derivatives for this indication.^[4]

Adverse effects by frequency:^[1][3][5][6]

Very common (>10% frequency):

• Nausea

Common (1-10% frequency):

Uncommon (0.1-1% frequency):

^‡ These are adverse effects only seen in patients with grade 3 or 4 chronic kidney disease. ^† These are adverse effects only seen in patients with grade 5 chronic kidney disease.

Contraindications include:^[6]

• Vitamin D intoxication
• Hypercalcaemia
• Hypersensitivity to paricalcitol or any of its excipients

whereas cautions include:^[1]

• Impaired liver function
• It is also advised that physicians regularly monitor their patients' calcium and phosphorus levels.

Drugs that may interact with paricalcitol include:^[1][6]

Electrolyte abnormalities (e.g. hypercalcaemia and hyperphosphataemia) are common overdose symptoms.^[6] Treatment is mostly supportive, with particular attention being paid to correcting electrolyte anomalies and reducing intake of calcium in both the form of supplementation and diet.^[6] As it is so heavily bound to plasma proteins haemodialysis is unlikely to be helpful in cases of overdose.^[6]

Early symptoms of overdose can include:^[6]

However, many of these symptoms are also indicative of kidney failure and hence may be masked by the patient's condition.^[6]

Late symptoms of overdose include:

Like 1,25-dihydroxyergocalciferol, paricalcitol acts as an agonist at the vitamin D receptor and thereby lowers parathyroid hormone levels in the blood.^[1]

The plasma concentration of paricalcitol decreases rapidly and log-linearly within two hours after initial intravenous administration. Therefore, it is not expected to accumulate with multiple dosing, since paricalcitol is usually given no more frequently than every other day (3 times per week).^[7][8]