Page last updated: 2024-10-29

ketoconazole and Hyperparathyroidism, Secondary

ketoconazole has been researched along with Hyperparathyroidism, Secondary in 2 studies

1-acetyl-4-(4-{[2-(2,4-dichlorophenyl)-2-(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy}phenyl)piperazine : A dioxolane that is 1,3-dioxolane which is substituted at positions 2, 2, and 4 by imidazol-1-ylmethyl, 2,4-dichlorophenyl, and [para-(4-acetylpiperazin-1-yl)phenoxy]methyl groups, respectively.

Hyperparathyroidism, Secondary: Abnormally elevated PARATHYROID HORMONE secretion as a response to HYPOCALCEMIA. It is caused by chronic KIDNEY FAILURE or other abnormalities in the controls of bone and mineral metabolism, leading to various BONE DISEASES, such as RENAL OSTEODYSTROPHY.

Research Excerpts

ExcerptRelevanceReference
"The calcimimetic cinacalcet hydrochloride (cinacalcet) is used for treatment of patients with chronic kidney disease with secondary hyperparathyroidism, a population that commonly receives multiple concurrent medications."5.12Pharmacokinetics of cinacalcet hydrochloride when administered with ketoconazole. ( Harris, RZ; Padhi, D; Salfi, M; Sullivan, JT, 2007)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Harris, RZ1
Salfi, M1
Sullivan, JT1
Padhi, D1
Kawahara, M1
Iwasaki, Y1
Sakaguchi, K1
Taguchi, T1
Nishiyama, M1
Nigawara, T1
Tsugita, M1
Kambayashi, M1
Suda, T1
Hashimoto, K1

Trials

1 trial available for ketoconazole and Hyperparathyroidism, Secondary

ArticleYear
Pharmacokinetics of cinacalcet hydrochloride when administered with ketoconazole.
    Clinical pharmacokinetics, 2007, Volume: 46, Issue:6

    Topics: Administration, Oral; Adult; Analysis of Variance; Antifungal Agents; Area Under Curve; Calcium; Cin

2007

Other Studies

1 other study available for ketoconazole and Hyperparathyroidism, Secondary

ArticleYear
Predominant role of 25OHD in the negative regulation of PTH expression: clinical relevance for hypovitaminosis D.
    Life sciences, 2008, Mar-26, Volume: 82, Issue:13-14

    Topics: Animals; Base Sequence; Cell Line; Cloning, Molecular; Enzyme Inhibitors; Feedback, Physiological; G

2008