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

NCT02312544 · ClinicalTrials.gov registry record · Phase 2

Phase 2b Study Evaluating Safety and Efficacy of OTX-TP Compared to Timolol Drops in the Treatment of Subjects With Open Angle Glaucoma or Ocular Hypertension

A Phase 2 study, sponsored by Ocular Therapeutix.

Completed
Registry status
Phase 2
Development phase
72
Enrollment target

NCT02312544: Completed Phase 2 study, sponsored by Ocular Therapeutix.

NCT02312544 is a Phase 2 study that has completed, run by Ocular Therapeutix. The registered enrollment target is 72 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (46% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02312544, a Phase 2 study, has completed, sponsored by Ocular Therapeutix.

COMPLETED
Registry status
Phase 2
Development phase
72 participants
Enrollment target

Study Summary

To evaluate the safety and IOP lowering efficacy of OTX-TP, a sustained release travoprost drug product, placed in the canaliculus of the eyelid compared to Timolol Maleate Ophthalmic Solution, 0.5% in the treatment of subjects with open angle glaucoma or ocular hypertension. The study is designed to assess clinically meaningful response to treatment and is not powered to measure any efficacy endpoints with statistical significance.

Interventions

  • DRUG Timolol
  • DRUG OTX-TP

Trial Details

FieldValue
Enrollment Target 72 participants
Start Date 2014-11
Est. Completion 2015-12
Phase Phase 2
Ocular Therapeutix

20 total trials

What the finished NCT02312544 record still lists

NCT02312544 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 72 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (46% lower).

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

NCT02312544 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02312544 about?

NCT02312544 is a clinical study titled "Phase 2b Study Evaluating Safety and Efficacy of OTX-TP Compared to Timolol Drops in the Treatment of Subjects With Open Angle Glaucoma or Ocular Hypertension". To evaluate the safety and IOP lowering efficacy of OTX-TP, a sustained release travoprost drug product, placed in the canaliculus of the eyelid compared to Timolol Maleate Ophthalmic Solution, 0.5% in the treatment of subjects with open angle glaucoma or ocular hypertension. The study is designed t...

What is the current status of trial NCT02312544?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 72 participants. The study started on 2014-11. Estimated completion is 2015-12.

What interventions are being tested in trial NCT02312544?

The interventions under investigation include: Timolol (DRUG), OTX-TP (DRUG).

Who is sponsoring clinical trial NCT02312544?

This trial is sponsored by Ocular Therapeutix, which has 20 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02312544's enrollment target sits among peer trials

72 925th of 2000 higher than 1,065 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02359253 · 72 participants · NA

    Robot Aided Rehabilitation - Intervention

  • NCT02962661 · 72 participants · Phase 1

    Donor Bone Marrow Derived Mesenchymal Stem Cells in Controlling Heart Failure in Patients With Cardiomyopathy Caused by Anthracyclines

  • NCT03113643 · 72 participants · Phase 1

    SL-401 in Combination With Azacitidine or Azacitidine/Venetoclax in Acute Myeloid Leukemia (AML), High-Risk Myelodysplastic Syndrome (MDS) or Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN)

  • NCT03187535 · 72 participants · NA

    Effect of TEAS on PONV After Spinal Surgery

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02312544, the US trial registry maintained by the National Library of Medicine. NCT02312544 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.