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Paricalcitol: Zemplar®

Hospital Universitario de Canarias · FDA-approved active Small molecule

Paricalcitol is a selective vitamin D receptor agonist that activates the vitamin D receptor to regulate calcium and phosphate homeostasis and suppress parathyroid hormone secretion.

Paricalcitol is a selective vitamin D receptor agonist that activates the vitamin D receptor to regulate calcium and phosphate homeostasis and suppress parathyroid hormone secretion. Used for Secondary hyperparathyroidism in patients with chronic kidney disease on hemodialysis, Secondary hyperparathyroidism in patients with chronic kidney disease stages 3-4 (non-dialysis).

At a glance

Generic nameParicalcitol: Zemplar®
Also known asC
SponsorHospital Universitario de Canarias
Drug classVitamin D receptor agonist
TargetVitamin D receptor (VDR)
ModalitySmall molecule
Therapeutic areaNephrology / Endocrinology
PhaseFDA-approved

Mechanism of action

Paricalcitol binds to and activates the vitamin D receptor (VDR), a nuclear receptor that regulates gene expression involved in calcium and phosphate metabolism. By activating VDR in the parathyroid glands, it suppresses parathyroid hormone (PTH) production, thereby reducing secondary hyperparathyroidism. Unlike calcitriol, paricalcitol has selective VDR activation with reduced effects on intestinal calcium absorption and bone resorption, resulting in a better therapeutic window.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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