WHO ICTRP trial

The human bioequivalence test of Epalrestai Tablets

ChiCTR2100041820 · Chinese Clinical Trial Registry (ChiCTR) · Not Recruiting

Key facts

Trial ID ChiCTR2100041820
Public title The human bioequivalence test of Epalrestai Tablets
Scientific title Single-center, randomized, double-cycle, double-cross-design trial for evaluation of human bioequivalence for a single oral Epalrestai Tablets in Chinese healthy subjects under fasting conditions
Primary sponsor Jiangsu Integrated Traditional Chinese and Western Medicine Hospital
Registry Chinese Clinical Trial Registry (ChiCTR)
Recruitment status Not Recruiting
Study type Interventional study
Phase 1
Countries China
Conditions Diabetic neuropathy
Interventions fasting congdition (pre-test):After fasting for at least 10 hours overnight, on the morning of the test day, one of the test preparations or one of the reference preparations was taken on an empty stomach with 240mL water. The drug was…
Registration date Jan 6, 2021
Target size fasting congdition (pre-test):6;fasting congdition:28
Registry page chictr.org.cn

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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