WHO ICTRP trial

A single-center, open-label, randomized, single-dose, two-cycle, two-sequence…

ChiCTR2100054331 · Chinese Clinical Trial Registry (ChiCTR) · Not Recruiting

Key facts

Trial ID ChiCTR2100054331
Public title A single-center, open-label, randomized, single-dose, two-cycle, two-sequence, crossover bioequivalence study to evaluate the effects of the test preparation apremilast tablets and reference preparation apremilast tablets in healthy adult subjects in the fasting/postprandial state
Scientific title A single-center, open-label, randomized, single-dose, two-cycle, two-sequence, crossover bioequivalence study to evaluate the effects of the test preparation apremilast tablets and reference preparation apremilast tablets in healthy adult subjects in the fasting/postprandial state
Primary sponsor Huzhou Central Hospital
Registry Chinese Clinical Trial Registry (ChiCTR)
Recruitment status Not Recruiting
Study type Interventional study
Countries China
Conditions Psoriasis
Interventions Fasting group A (T-R):Take the test preparation first and then take the reference reagent;Fasting group B (R-T):Take the reference reagent first and then take the test preparation;Postprandial group A (T-R):Take the test preparation first…
Registration date Dec 14, 2021
Target size Fasting group A (T-R):8;Fasting group B (R-T):8;Postprandial group A…
Registry page chictr.org.cn

At a glance

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

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