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Relative Bioavailability of ESK-001 Tablet Versus Liquid in Healthy Participants

Pharmacokinetics Clinical Trial

Official title:
The Relative Bioavailability of an ESK-001 Tablet Versus Liquid Formulation, and the Effect of Food or Gastric Acid Reduction on the Pharmacokinetics of ESK-001 in Healthy Participants

Clinical Trial Summary

This is a single-center, in-house, open-label, crossover study in 15 healthy participants.

Clinical Trial Description

This clinical trial information was submitted voluntarily under the applicable law and, therefore, certain submission deadlines may not apply. (That is, clinical trial information for this applicable clinical trial was submitted under section 402(j)(4)(A) of the Public Health Service Act and 42 CFR 11.60 and is not subject to the deadlines established by sections 402(j)(2) and (3) of the Public Health Service Act or 42 CFR 11.24 and 11.44.) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05330858
Study type Interventional
Source Alumis Inc
Contact
Status Completed
Phase Phase 1
Start date March 17, 2022
Completion date September 20, 2022
View Details
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