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NCT05389267 · ClinicalTrials.gov registry record · Phase 1

Safety Assessment of T4090 Eye Drops in Ocular Hypertensive or Glaucomatous Patients.

A Phase 1 study of Glaucoma and Ocular Hypertension, sponsored by Laboratoires Thea.

Active
Registry status
Phase 1
Development phase
120
Enrollment target
1
Study location

NCT05389267: Active Phase 1 study of Glaucoma and Ocular Hypertension, sponsored by Laboratoires Thea.

NCT05389267 is a Phase 1 study of Glaucoma and Ocular Hypertension that is active but no longer recruiting, run by Laboratoires Thea. The registered enrollment target is 120 participants, below the 909-participant average among 92 other Glaucoma trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05389267, a Phase 1 study of Glaucoma and Ocular Hypertension, is active but no longer recruiting, sponsored by Laboratoires Thea.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
120 participants
Enrollment target
1
Study location

Study Summary

The study purpose is to evaluate the safety of T4090.

Primary Outcome

Ocular and systemic treatment-emergent adverse events, serious TEAE, IMP-related TEAE, TEAE leading to premature IMP discontinuation.

Interventions

  • DRUG Placebo
  • DRUG Kinezodianone R hydrochloride

Study Locations (1)

California

  • Dr EL-HARAZI - Glendale

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2022-07-05
Est. Completion 2024-12-31
Phase Phase 1
Laboratoires Thea

11 total trials

What the registry record for NCT05389267 still lists

NCT05389267 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 909-participant average among 92 other Glaucoma trials with a reported enrollment target (87% lower).

The record links to 2 conditions, with Glaucoma appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT05389267 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT05389267 about?

NCT05389267 is a clinical study titled "Safety Assessment of T4090 Eye Drops in Ocular Hypertensive or Glaucomatous Patients.". The study purpose is to evaluate the safety of T4090.

What is the current status of trial NCT05389267?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 120 participants. The study started on 2022-07-05. Estimated completion is 2024-12-31.

What conditions does trial NCT05389267 study?

This clinical trial studies the following conditions: Glaucoma, Ocular Hypertension.

What interventions are being tested in trial NCT05389267?

The interventions under investigation include: Placebo (DRUG), Kinezodianone R hydrochloride (DRUG).

Who is sponsoring clinical trial NCT05389267?

This trial is sponsored by Laboratoires Thea, which has 11 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05389267 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Glaucoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05389267's enrollment target sits among peer trials

120 38th of 92 higher than 55 of 92 other Glaucoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Glaucoma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05389267, the US trial registry maintained by the National Library of Medicine. NCT05389267 (mid enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.