MedPath

Calcitriol

Generic Name
Calcitriol
Brand Names
Rocaltrol, Vectical
Drug Type
Small Molecule
Chemical Formula
C27H44O3
CAS Number
32222-06-3
Unique Ingredient Identifier
FXC9231JVH

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

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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