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NCT02531152 · ClinicalTrials.gov registry record · Phase 1

28-Day Repeated Topical Study to Evaluate the Safety and Activity of 5 Escalating Dose Levels of SAR366234 and One Dose of Latanoprost in Patients With Open Angle Glaucoma or Ocular Hypertension

A Phase 1 study, sponsored by Sanofi.

Completed
Registry status
Phase 1
Development phase
54
Enrollment target

NCT02531152 is a Phase 1 study that has completed, run by Sanofi. The registered enrollment target is 54 participants.

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The verdict

NCT02531152, a Phase 1 study, has completed, sponsored by Sanofi.

COMPLETED
Registry status
Phase 1
Development phase
54 participants
Enrollment target

Study Summary

Primary Objective: To assess the local and systemic safety and tolerability of ascending repeated topical doses of SAR366234 monotherapy in patients with open angle glaucoma (OAG) or ocular hypertension (OHT) as compared to latanoprost. Secondary Objective: To assess the pharmacodynamic activity of ascending repeated topical doses of SAR366234 in patients with OAG or OHT as compared to latanoprost.

Interventions

  • DRUG Latanoprost
  • DRUG SAR366234

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2015-09
Est. Completion 2016-04
Phase Phase 1

Sponsor

Sanofi

713 total trials

What the Registry Record Tells You About NCT02531152

The ClinicalTrials.gov registry entry for NCT02531152 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 54 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sanofi, which has 713 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Latanoprost is the first listed.

NCT02531152 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02531152 about?

NCT02531152 is a clinical study titled "28-Day Repeated Topical Study to Evaluate the Safety and Activity of 5 Escalating Dose Levels of SAR366234 and One Dose of Latanoprost in Patients With Open Angle Glaucoma or Ocular Hypertension". Primary Objective: To assess the local and systemic safety and tolerability of ascending repeated topical doses of SAR366234 monotherapy in patients with open angle glaucoma (OAG) or ocular hypertension (OHT) as compared to latanoprost. Secondary Objective: To assess the pharmacodynamic activity ...

What is the current status of trial NCT02531152?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 54 participants. The study started on 2015-09. Estimated completion is 2016-04.

What interventions are being tested in trial NCT02531152?

The interventions under investigation include: Latanoprost (DRUG), SAR366234 (DRUG).

Who is sponsoring clinical trial NCT02531152?

This trial is sponsored by Sanofi, which has 713 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.