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NCT05325346

A Phase I Study of the Co-administration of VLX-1005 and Argatroban in Healthy Human Subjects

Completed Phase 1 Last updated 11 January 2023
What this trial tests

Phase 1 trial testing VLX-1005 in Heparin-induced Thrombocytopenia in 12 participants. Completed in 14 April 2022.

Timeline
7 March 2022
Primary endpoint
1 April 2022
14 April 2022

Quick facts

Lead sponsorVeralox Therapeutics
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposetreatment
Enrollment12
Start date7 March 2022
Primary completion1 April 2022
Estimated completion14 April 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Veralox Therapeutics

Who can join

Adults 19 to 55, any sex, with Heparin-induced Thrombocytopenia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study is designed to characterize the safety and tolerability of VLX-1005 and argatroban administered intravenously, either alone or in combination; and the pharmacokinetics and pharmacodynamics and potential interaction of both agents in a population of healthy subjects.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. VLX-1005, but not argatroban, prevents ITAM-mediated platelet activation and heparin-induced thrombocytopenia.
    Yamaguchi A, Putzbach V, Adili R, Lazar S, et al · · 2026 · PMID 41909515 · DOI 10.1016/j.bvth.2026.100146

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Other trials of VLX-1005

Trials testing the same drug.

Other Veralox Therapeutics trials

Trials by the same sponsor.

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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/NCT05325346.

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