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Effects of single dose rifampin on the Pharmacokinetics and Pharmacodynamics of Repaglinide in Relation to SLC21A6 521T>C Polymorphism

pharmacogenomics

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ION-15005782
Enrollment
Unknown
Registered
2014-11-10
Start date
2014-12-05
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endocrine disease

Interventions

two:rifampicin+repaglinide

Sponsors

the Third Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
19 Years to 24 Years

Inclusion criteria

Inclusion criteria: Male, 18-40 years of age (including boundary value); subjects body mass index (BMI): 19-26 (including boundary value); According to the medical examination, vital signs, electrocardiogram and clinical laboratory result, participants are healthy, and the inspection was taken 1 week before the drug administration; subjects are able to read and understand the contents of the informed consent, and sign the informed consent before any research related operations; subjects are not taken any other drugs two weeks before the test.

Exclusion criteria

Exclusion criteria: Subjects with arrhythmia, bronchial or cardiovascular disease history, gastric disease, thyrotoxicosis, Parkinson's syndrome, or any other disease or physiology that can interference test results; with disease that can affect drug absorption or metabolic disease of the gastrointestinal tract; have drug abuse history or positive urine drug test results in the past one year; used other medicines within 14 days before the test; participated in other drug experiments within 30 days before the test; Serious blood loss or donation (500 ml) within 3 months before the test.

Design outcomes

Primary

MeasureTime frame
blood glucose concentration;

Countries

China

Contacts

Public ContactCheng-Xian Guo
gchxyy@163.com+86 0731-88618338

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026