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NCT05330858
Relative Bioavailability of ESK-001 Tablet Versus Liquid in Healthy Participants
Phase 1 trial testing ESK-001 in Pharmacokinetics in 14 participants. Completed in 20 September 2022.
30 June 2022
Quick facts
| Lead sponsor | Alumis Inc |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | none |
| Primary purpose | basic science |
| Enrollment | 14 |
| Start date | 17 March 2022 |
| Primary completion | 30 June 2022 |
| Estimated completion | 20 September 2022 |
| Sites | 1 location across United States |
Drugs / interventions tested
- ESK-001 — full drug profile →
- Rabeprazole — full drug profile →
Conditions studied
- Pharmacokinetics — all drugs for Pharmacokinetics →
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.
Verify or expand the search:
- PubMed search for NCT05330858
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of ESK-001
Trials testing the same drug.
- NCT06962774 — An Investigational Study of ESK-001 in Participants With Normal Renal Function and Participants With Mild, Moderate, and · Phase 1 · completed
- NCT07378579 — An Investigational Study to Evaluate the Cardiac Safety Assessment (TQTc Study) of ESK-001 · Phase 1 · completed
- NCT05953688 — POC Study to Evaluate the Efficacy and Safety of ESK-001 in Patients With Active Intermediate, Posterior, or Pan NIU · Phase 2 · terminated
- NCT05600036 — A Study to Evaluate the Efficacy and Safety of ESK-001 in Patients With Plaque Psoriasis · Phase 2 · completed
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Other Alumis Inc trials
Trials by the same sponsor.
- NCT06962774 — An Investigational Study of ESK-001 in Participants With Normal Renal Function and Participants With Mild, Moderate, and · Phase 1 · completed
- NCT06588738 — A Study in Patients With Moderate to Severe Plaque Psoriasis to Evaluate the Efficacy and Safety of ESK-001 · Phase 3 · completed
- NCT06586112 — A Study to Evaluate the Efficacy and Safety of ESK-001 in Patients With Moderate to Severe Plaque Psoriasis · Phase 3 · completed
- NCT07378579 — An Investigational Study to Evaluate the Cardiac Safety Assessment (TQTc Study) of ESK-001 · Phase 1 · completed
- NCT07442149 — An Investigational Study to Evaluate the Safety and Tolerability of Single and Multiple Ascending Doses of A-005 · Phase 1 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05330858 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Alumis Inc
- Last refreshed: 9 May 2023
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