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NCT05298046

Study of TAVO101 in Healthy Volunteers

Completed Phase 1 Last updated 19 November 2024
What this trial tests

Phase 1 trial testing Experimental: TAVO101 in Healthy Subjects in 42 participants. Completed in 30 September 2024.

Timeline
11 May 2022
Primary endpoint
1 June 2024
30 September 2024

Quick facts

Lead sponsorTavotek Biotherapeutics
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeprevention
Enrollment42
Start date11 May 2022
Primary completion1 June 2024
Estimated completion30 September 2024
Sites1 location across Australia

Drugs / interventions tested

Conditions studied

Sponsor

Tavotek Biotherapeutics — full company profile →

Who can join

Adults 18 to 65, any sex, with Healthy Subjects. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a Phase 1, single ascending dose study designed to investigate TAVO101, administered as an IV infusion in healthy subjects. This study is designed to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of TAVO101.

Publications & conference data

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

  1. Potential of alarmin-targeted bispecific and combination therapies in airway disease.
    Komori HK, Ortega H. · · 2025 · PMID 41409758 · DOI 10.3389/falgy.2025.1700060

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Other recruiting trials for Healthy Subjects

Currently open trials in the same condition.

Other Tavotek Biotherapeutics 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/NCT05298046.

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