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Paricalcitol, atorvastatin

Ricardo Mouzo Mirco · Phase 3 active Small molecule

This combination uses paricalcitol to activate vitamin D receptors for mineral metabolism regulation and atorvastatin to inhibit HMG-CoA reductase for cholesterol lowering.

This combination uses paricalcitol to activate vitamin D receptors for mineral metabolism regulation and atorvastatin to inhibit HMG-CoA reductase for cholesterol lowering. Used for Secondary hyperparathyroidism in chronic kidney disease patients with dyslipidemia.

At a glance

Generic nameParicalcitol, atorvastatin
Also known asG2
SponsorRicardo Mouzo Mirco
Drug classVitamin D receptor activator + HMG-CoA reductase inhibitor (statin)
TargetVitamin D receptor (VDR) + HMG-CoA reductase
ModalitySmall molecule
Therapeutic areaNephrology / Cardiovascular
PhasePhase 3

Mechanism of action

Paricalcitol is a selective vitamin D receptor activator that regulates calcium and phosphate homeostasis, particularly useful in chronic kidney disease. Atorvastatin is a statin that reduces LDL cholesterol by inhibiting hepatic cholesterol synthesis. Together, they address both mineral-bone metabolism and cardiovascular risk in patients with kidney disease.

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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