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NCT01960010 · ClinicalTrials.gov registry record · Phase 3

A Safety and Efficacy Study of MIM-D3 Ophthalmic Solution for the Treatment of Dry Eye

A Phase 3 study, sponsored by Mimetogen Pharmaceuticals USA.

Completed
Registry status
Phase 3
Development phase
403
Enrollment target

NCT01960010: Completed Phase 3 study, sponsored by Mimetogen Pharmaceuticals USA.

NCT01960010 is a Phase 3 study that has completed, run by Mimetogen Pharmaceuticals USA. The registered enrollment target is 403 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (48% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01960010, a Phase 3 study, has completed, sponsored by Mimetogen Pharmaceuticals USA.

COMPLETED
Registry status
Phase 3
Development phase
403 participants
Enrollment target

Study Summary

The purpose of this study is to assess the safety and efficacy of MIM-D3 Ophthalmic Solution compared with Placebo Ophthalmic Solution in treating the signs and symptoms of dry eye.

Interventions

  • DRUG Vehicle
  • DRUG MIM-D3 Ophthalmic Solution

Trial Details

FieldValue
Enrollment Target 403 participants
Start Date 2013-10
Est. Completion 2014-08
Phase Phase 3
Mimetogen Pharmaceuticals USA

6 total trials

What the finished NCT01960010 record still lists

NCT01960010 is an interventional study that assigns participants to a tested intervention. The registered 403 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (48% lower).

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

NCT01960010 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01960010 about?

NCT01960010 is a clinical study titled "A Safety and Efficacy Study of MIM-D3 Ophthalmic Solution for the Treatment of Dry Eye". The purpose of this study is to assess the safety and efficacy of MIM-D3 Ophthalmic Solution compared with Placebo Ophthalmic Solution in treating the signs and symptoms of dry eye.

What is the current status of trial NCT01960010?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 403 participants. The study started on 2013-10. Estimated completion is 2014-08.

What interventions are being tested in trial NCT01960010?

The interventions under investigation include: Vehicle (DRUG), MIM-D3 Ophthalmic Solution (DRUG).

Who is sponsoring clinical trial NCT01960010?

This trial is sponsored by Mimetogen Pharmaceuticals USA, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01960010's enrollment target sits among peer trials

403 917th of 2000 higher than 1,082 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT01960010, the US trial registry maintained by the National Library of Medicine. NCT01960010 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.