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COMPLETED Phase 2

A Safety And Efficacy Study Of Alg-1001 In Human Subjects With Symptomatic Focal Vitreomacular Adhesion

NCT02153476 · View on ClinicalTrials.gov ↗

Study Summary

Evaluate the safety and efficacy of ophthalmic intravitreal injection of ALG-1001 in human subjects with symptomatic focal vitreomacular adhesion

Interventions

  • DRUG 2.0mg of ALG-1001
  • DRUG Balanced Salt Solution

Study Locations (5)

California

  • Retina-Vitreous Associates Medical Group — Beverly Hills
  • California Retina Consultants — Santa Barbara

Texas

  • Austin Retina Associates — Austin
  • Retina Consultants Houston — Houston

Florida

  • Center for Retinal and Macular Disease — Winter Haven

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2014-02
Est. Completion 2015-06
Phase Phase 2

Sponsor

Allegro Ophthalmics

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02153476

The ClinicalTrials.gov registry entry for NCT02153476 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Allegro Ophthalmics, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Symptomatic Focal Vitreomacular Adhesion appearing as the primary indexed condition, and to 2 interventions — of which 2.0mg of ALG-1001 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02153476 reports 5 study locations spanning 3 distinct geographic areas — top geographies include California, Texas, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02153476 about?

NCT02153476 is a clinical study titled "A Safety And Efficacy Study Of Alg-1001 In Human Subjects With Symptomatic Focal Vitreomacular Adhesion". Evaluate the safety and efficacy of ophthalmic intravitreal injection of ALG-1001 in human subjects with symptomatic focal vitreomacular adhesion

What is the current status of trial NCT02153476?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 45 participants. The study started on 2014-02. Estimated completion is 2015-06.

What conditions does trial NCT02153476 study?

This clinical trial studies the following conditions: Symptomatic Focal Vitreomacular Adhesion. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02153476?

The interventions under investigation include: 2.0mg of ALG-1001 (DRUG), Balanced Salt Solution (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02153476?

This trial is sponsored by Allegro Ophthalmics, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02153476 being conducted?

This trial has 5 study locations across California, Florida, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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