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NCT05330858

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

Completed Phase 1 Last updated 9 May 2023
What this trial tests

Phase 1 trial testing ESK-001 in Pharmacokinetics in 14 participants. Completed in 20 September 2022.

Timeline
17 March 2022
Primary endpoint
30 June 2022
20 September 2022

Quick facts

Lead sponsorAlumis Inc
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposebasic science
Enrollment14
Start date17 March 2022
Primary completion30 June 2022
Estimated completion20 September 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Alumis Inc — full company profile →

Who can join

Adults 18 to 60, any sex, with Pharmacokinetics. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of ESK-001

Trials testing the same drug.

Other recruiting trials for Pharmacokinetics

Currently open trials in the same condition.

Other Alumis Inc trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05330858.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing