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NCT05848128

Efficacy and Safety Evaluation of Tavilermide Ophthalmic Solution for the Treatment of Dry Eye

Completed Phase 3 Last updated 10 June 2024
What this trial tests

Phase 3 trial testing 5% Tavilermide ophthalmic solution in Dry Eye Syndromes in 642 participants. Completed in 11 May 2024.

Timeline
28 June 2023
Primary endpoint
11 May 2024
11 May 2024

Quick facts

Lead sponsorMimetogen Pharmaceuticals USA, Inc.
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment642
Start date28 June 2023
Primary completion11 May 2024
Estimated completion11 May 2024
Sites29 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Mimetogen Pharmaceuticals USA, Inc. — full company profile →

Who can join

18 and older, any sex, with Dry Eye Syndromes or Dry Eye Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of the study is to compare the efficacy and safety of 5% tavilermide ophthalmic solution to placebo for the treatment of the signs and symptoms of dry eye disease.

Publications & conference data

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

  1. Advance in peptide-based drug development: delivery platforms, therapeutics and vaccines.
    Xiao W, Jiang W, Chen Z, Huang Y, et al · · 2025 · cited 144× · PMID 40038239 · DOI 10.1038/s41392-024-02107-5

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Other recruiting trials for Dry Eye Syndromes

Currently open trials in the same condition.

Other Mimetogen Pharmaceuticals USA, 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/NCT05848128.

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