Overview
Calcitriol is an active metabolite of vitamin D with 3 hydroxyl (OH) groups and is commonly referred to as 1,25-dihydroxycholecalciferol, or 1alpha,25-dihydroxyvitamin D, 1,25-dihydroxyvitamin D. It is produced in the body after series of conversion steps of 7-dehydrocholesterol from exposure to UV light. 7-dehydrocholesterol is converted to Vitamin D3 (vitamin D3) in the skin, which is then converted to Calcifediol in the liver and kidneys. Calcifediol undergoes hydroxylation to form calcitriol via 1α-hydroxylase (CYP27B1) activity . Calcitriol is considered to be the most potent metabolite of vitamin D in humans . Renal production of calcitriol is stimulated in response to PTH, low calcium and low phosphate . Calcitriol plays a role in plasma calcium regulation in concert with parathyroid hormone (PTH) by enhancing absorption of dietary calcium and phosphate from the gastrointestinal tract, promoting renal tubular reabsorption of calcium in the kidneys, and stimulating the release of calcium stores from the skeletal system. In addition to promoting fatty acid synthesis and inhibiting lipolysis, calcitriol has been demonstrated to increase energy efficiency by suppressing UCP2 expression, which is modulated by signaling pathways of classical nuclear receptors (nVDR), where calcitriol acts as a natural ligand . There is also evidence that calcitriol modulates the action of cytokines and may regulate immune and inflammatory response, cell turnover, cell differentiation . Administered orally and intravenously, calcitriol is commonly used as a medication in the treatment of secondary hyperparathyroidism and resultant metabolic bone disease, hypocalcemia in patients undergoing chronic renal dialysis, and osteoporosis. It is also available in topical form for the treatment of mild to moderate plaque psoriasis in adults. Calcitriol is marketed under various trade names including Rocaltrol (Roche), Calcijex (Abbott) and Decostriol (Mibe, Jesalis).
Indication
Used to treat vitamin D deficiency or insufficiency, refractory rickets (vitamin D resistant rickets), familial hypophosphatemia and hypoparathyroidism, and in the management of hypocalcemia and renal osteodystrophy in patients with chronic renal failure undergoing dialysis. Also used in conjunction with calcium in the management and prevention of primary or corticosteroid-induced osteoporosis.
Associated Conditions
- Hypocalcemia
- Mild to Moderate Plaque Psoriasis
- Osteodystrophy
- Secondary Hyperparathyroidism (SHPT)
- Vitamin D Resistant Rickets
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2023/06/13 | Phase 4 | Recruiting | Shanghai Jiao Tong University Affiliated Sixth People's Hospital | ||
2023/03/13 | Phase 2 | Completed | |||
2022/06/13 | Not Applicable | UNKNOWN | |||
2022/03/28 | Not Applicable | UNKNOWN | |||
2022/01/21 | Not Applicable | Completed | |||
2021/07/19 | Not Applicable | Completed | |||
2021/04/01 | Early Phase 1 | Terminated | |||
2021/03/17 | Phase 4 | Completed | Berta Alemany | ||
2020/11/19 | Not Applicable | Completed | |||
2020/05/13 | Phase 1 | Terminated |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Validus Pharmaceuticals LLC | 30698-143 | ORAL | 0.25 ug in 1 1 | 12/13/2023 | |
Strides Pharma Science Limited | 64380-724 | ORAL | 0.5 ug in 1 1 | 3/28/2022 | |
Carilion Materials Management | 68151-0088 | ORAL | 0.25 ug in 1 1 | 8/31/2011 | |
Akorn | 17478-931 | INTRAVENOUS | 1 ug in 1 mL | 11/20/2017 | |
Padagis Israel Pharmaceuticals Ltd | 45802-608 | TOPICAL | 3 ug in 1 g | 2/22/2023 | |
Atlantic Biologicals Corps | 17856-0723 | ORAL | 0.25 ug in 1 1 | 12/29/2016 | |
Sun Pharmaceutical Industries, Inc. | 63304-239 | ORAL | 0.25 ug in 1 1 | 8/22/2018 | |
Amneal Pharmaceuticals LLC | 65162-519 | ORAL | 0.25 ug in 1 1 | 12/18/2023 | |
Bryant Ranch Prepack | 63629-8741 | ORAL | 0.25 ug in 1 1 | 8/30/2019 | |
Akorn | 17478-831 | INTRAVENOUS | 1 ug in 1 mL | 10/3/2013 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
SILKIS OINTMENT 3 mcg/g | SIN12160P | OINTMENT | 3 mcg/g | 12/30/2002 | |
MEDITROL | SIN13449P | CAPSULE, LIQUID FILLED | 0.25 MCG | 4/25/2008 | |
ROCALTROL CAPSULE 0.25 mcg | SIN03865P | CAPSULE, LIQUID FILLED | 0.25 mcg | 2/10/1990 | |
RASPUTIN SOFT CAPSULE 0.25 mcg | SIN12258P | CAPSULE, LIQUID FILLED | 0.25 mcg | 4/25/2003 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
OSTEODIOL CAP 0.5MCG | N/A | N/A | N/A | 5/19/2004 | |
SILKIS OINTMENT 3MCG/G | N/A | N/A | N/A | 12/31/2002 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
CALCITRIOL SG calcitriol 0.25 microgram capsule blister pack | 232771 | Medicine | A | 12/1/2015 | |
Calcitriol-AFT, calcitriol 0.25 microgram, capsule soft, bottle | 263800 | Medicine | A | 11/20/2015 | |
CALCITRIOL CW calcitriol 0.25 microgram capsule blister pack | 232768 | Medicine | A | 12/1/2015 | |
Calcitriol-RJIC calcitriol 0.25 microgram capsule blister pack | 423275 | Medicine | A | 1/5/2024 | |
ROCALTROL calcitriol 0.25 microgram capsule blister pack | 92969 | Medicine | A | 3/18/2003 | |
CALCIPROX calcitriol 0.25 microgram capsule bottle | 149505 | Medicine | A | 9/25/2008 | |
CALCITRIOL-GA calcitriol 0.25 microgram capsule blister pack | 224866 | Medicine | A | 8/21/2014 | |
CALITROL calcitriol 0.25 microgram capsule blister pack | 232770 | Medicine | A | 12/1/2015 | |
Calcitriol-DWRN calcitriol 0.25 microgram capsule blister pack | 423251 | Medicine | A | 1/5/2024 | |
Calcitriol-AFT, calcitriol 0.50 microgram, capsule soft, bottle | 263852 | Medicine | A | 11/20/2015 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
TARO-CALCITRIOL | 02485729 | Capsule - Oral | 0.5 MCG | 6/3/2019 | |
ROCALTROL | searchlight pharma inc | 00481823 | Capsule - Oral | 0.25 MCG | 12/31/1979 |
PMS-CALCITRIOL | 02495899 | Capsule - Oral | 0.25 MCG | 3/9/2020 | |
SILKIS | galderma canada inc | 02338572 | Ointment - Topical | 3 MCG / G | 4/9/2010 |
TARO-CALCITRIOL | 02485710 | Capsule - Oral | 0.25 MCG | 6/3/2019 | |
CALCITRIOL INJECTION USP | Sterimax Inc | 02399334 | Solution - Intravenous | 1 MCG / ML | 3/27/2015 |
ROCALTROL ORAL SOLUTION 1MCG/ML | Hoffmann-La Roche Limited | 00824291 | Solution - Oral | 1 MCG / ML | 12/31/1992 |
CALCIJEX | 00891738 | Solution - Intravenous | 1 MCG / ML | 12/31/1990 | |
ROCALTROL | searchlight pharma inc | 00481815 | Capsule - Oral | 0.5 MCG | 12/31/1979 |
CALCITRIOL-ODAN | odan laboratories ltd | 02431645 | Capsule - Oral | 0.5 MCG | 10/10/2014 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
ROCALTROL 0,25 mcg CAPSULAS BLANDAS | Atnahs Pharma Netherlands Bv. | 55973 | CÁPSULA BLANDA | Diagnóstico Hospitalario | Commercialized |
ROCALTROL 0,50 mcg CAPSULAS BLANDAS | Atnahs Pharma Netherlands Bv. | 55974 | CÁPSULA BLANDA | Diagnóstico Hospitalario | Commercialized |
CALCITRIOL KERN PHARMA 1 microgramo/ml SOLUCION INYECTABLE EFG | 68934 | SOLUCIÓN INYECTABLE | Uso Hospitalario | Commercialized | |
SILKIS 3 microgramos /g POMADA | Laboratorios Galderma S.A. | 64527 | POMADA | Medicamento Sujeto A Prescripción Médica | Commercialized |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
---|---|---|---|---|---|
No UK EMC drug information found for this drug. |
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