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NCT03739593 · ClinicalTrials.gov registry record · Phase 2

Study Assessing AR-1105 in Subjects With Macular Edema Due to Retinal Vein Occlusion (RVO)

A Phase 2 study, sponsored by Aerie Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
49
Enrollment target

NCT03739593: Completed Phase 2 study, sponsored by Aerie Pharmaceuticals.

NCT03739593 is a Phase 2 study that has completed, run by Aerie Pharmaceuticals. The registered enrollment target is 49 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (63% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT03739593, a Phase 2 study, has completed, sponsored by Aerie Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
49 participants
Enrollment target

Study Summary

This study will evaluate the safety, tolerability and efficacy of AR-1105 (dexamethasone implant) for the treatment of macular edema (ME) due to retinal vein occlusion (RVO). A more durable intravitreal implant containing a low dose of dexamethasone may result in less frequent retreatments, and potentially lower the incidence of steroid-related side effects without compromising efficacy.

Primary Outcome

Treatment-emergent adverse events summarized at the subject level by system organ class and preferred term are available in the Adverse Events module. Data reported in the table below corresponds to the total number of participants with ocular and non-ocular treatment-emergent adverse events (TEAEs).

Interventions

  • DRUG AR-1105-CF1
  • DRUG AR-1105-CF2

Trial Details

FieldValue
Enrollment Target 49 participants
Start Date 2019-03-13
Est. Completion 2020-07-09
Phase Phase 2
Aerie Pharmaceuticals

32 total trials

What the finished NCT03739593 record still lists

NCT03739593 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 49 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (63% lower).

The record links to 0 conditions, and to 2 interventions - of which AR-1105-CF1 is the first listed.

NCT03739593 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03739593 about?

NCT03739593 is a clinical study titled "Study Assessing AR-1105 in Subjects With Macular Edema Due to Retinal Vein Occlusion (RVO)". This study will evaluate the safety, tolerability and efficacy of AR-1105 (dexamethasone implant) for the treatment of macular edema (ME) due to retinal vein occlusion (RVO). A more durable intravitreal implant containing a low dose of dexamethasone may result in less frequent retreatments, and pote...

What is the current status of trial NCT03739593?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 49 participants. The study started on 2019-03-13. Estimated completion is 2020-07-09.

What interventions are being tested in trial NCT03739593?

The interventions under investigation include: AR-1105-CF1 (DRUG), AR-1105-CF2 (DRUG).

Who is sponsoring clinical trial NCT03739593?

This trial is sponsored by Aerie Pharmaceuticals, which has 32 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03739593's enrollment target sits among peer trials

49 1261st of 2000 higher than 736 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

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Source: ClinicalTrials.gov NCT03739593, the US trial registry maintained by the National Library of Medicine. NCT03739593 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.