Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05729594 · ClinicalTrials.gov registry record · Phase 1

Systemic Pharmacokinetic Study of T4032 (Unpreserved Bimatoprost 0.01%) Eye Gel Versus Lumigan® 0.01% Eye Drops in 40 Healthy Volunteers

A Phase 1 study, sponsored by Laboratoires Thea.

Completed
Registry status
Phase 1
Development phase
40
Enrollment target

NCT05729594 is a Phase 1 study that has completed, run by Laboratoires Thea. The registered enrollment target is 40 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05729594, a Phase 1 study, has completed, sponsored by Laboratoires Thea.

COMPLETED
Registry status
Phase 1
Development phase
40 participants
Enrollment target

Study Summary

This study is being performed to compare the systemic pharmacokinetic profiles of T4032 and Lumigan 0.01% given that T4032 has a different formulation (in terms of excipients) from the reference product.

Interventions

  • DRUG Bimatoprost Ophthalmic

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2023-02-27
Est. Completion 2023-04-05
Phase Phase 1

Sponsor

Laboratoires Thea

11 total trials

What the Registry Record Tells You About NCT05729594

The ClinicalTrials.gov registry entry for NCT05729594 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Laboratoires Thea, which has 11 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Bimatoprost Ophthalmic is the first listed.

NCT05729594 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05729594 about?

NCT05729594 is a clinical study titled "Systemic Pharmacokinetic Study of T4032 (Unpreserved Bimatoprost 0.01%) Eye Gel Versus Lumigan® 0.01% Eye Drops in 40 Healthy Volunteers". This study is being performed to compare the systemic pharmacokinetic profiles of T4032 and Lumigan 0.01% given that T4032 has a different formulation (in terms of excipients) from the reference product.

What is the current status of trial NCT05729594?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2023-02-27. Estimated completion is 2023-04-05.

What interventions are being tested in trial NCT05729594?

The interventions under investigation include: Bimatoprost Ophthalmic (DRUG).

Who is sponsoring clinical trial NCT05729594?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.