Hesperidin ( DrugBank: Hesperidin )


2 diseases
IDDisease name (Link within this page)Number of trials
46Malignant rheumatoid arthritis1
93Primary biliary cholangitis1

46. Malignant rheumatoid arthritis


Clinical trials : 4,356 Drugs : 2,567 - (DrugBank : 415) / Drug target genes : 192 - Drug target pathways : 228
No.TrialIDDate_
enrollment
Date_
registration
Public_titleScientific_titleConditionInterventionPrimary_
sponsor
Secondary_
sponsor
Recruitment_
Status
Inclusion_
agemin
Inclusion_
agemax
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gender
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size
PhaseCountries
1NCT05756179
(ClinicalTrials.gov)
July 202321/2/2023Effect of Diosmin and Hesperidin in Treatment of Patients With Rheumatoid ArthritisClinical Study Evaluating the Effect of Diosmin and Hesperidin in Treatment of Patients With Rheumatoid ArthritisRheumatoid ArthritisDrug: Diosmin and Hesperidin CombinationAlexandria UniversityNULLNot yet recruiting19 Years65 YearsAll80Phase 3NULL

93. Primary biliary cholangitis


Clinical trials : 298 Drugs : 252 - (DrugBank : 59) / Drug target genes : 35 - Drug target pathways : 115
No.TrialIDDate_
enrollment
Date_
registration
Public_titleScientific_titleConditionInterventionPrimary_
sponsor
Secondary_
sponsor
Recruitment_
Status
Inclusion_
agemin
Inclusion_
agemax
Inclusion_
gender
Target_
size
PhaseCountries
1JPRN-jRCTs051210210
30/03/202230/03/2022BIG STEPBenefit of glucosyl Hesperidin in patients with primary biliary cholangitis: amulticenter, open-label, randomized control study Primary Biliary Cholangitis
Cholangitis
Participants will be randomly assigned to standard dose and high dose groups.
In standard dose group, hesperidin tablet 500 mg (two tablets at a time once a day after meal) will be orally administered for 24 weeks. In high dose group, hesperidin tablet 1000mg (four tablets at a time once a day after meal) will be orally administered for 24 weeks.
Fujinaga HisayukiNULLRecruiting>= 20age oldNot applicableBoth110Phase 2Japan