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NCT00363714 · ClinicalTrials.gov registry record · Phase 1

A Dose Escalation Trial of an Intravitreal Injection of Sirna-027 in Patients With Subfoveal Choroidal Neovascularization (CNV) Secondary to Age-Related Macular Degeneration (AMD)

A Phase 1 study, sponsored by Allergan.

Completed
Registry status
Phase 1
Development phase
26
Enrollment target

NCT00363714 is a Phase 1 study that has completed, run by Allergan. The registered enrollment target is 26 participants.

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The verdict

NCT00363714, a Phase 1 study, has completed, sponsored by Allergan.

COMPLETED
Registry status
Phase 1
Development phase
26 participants
Enrollment target

Study Summary

The purpose of this study will be to assess the safety and tolerability and dose-limiting toxicity of a single intravitreal injection of Sirna-027 (AGN211745) and to assess the anatomical changes in the retina, changes in CNV, and changes in visual acuity. Escalation to the next dose cohort will be completed following minimum of 2 weeks follow-up. Patients will be monitored intensively for three months, and then followed-up for safety up to 24 months post-injection.

Interventions

  • DRUG AGN211745

Trial Details

FieldValue
Enrollment Target 26 participants
Start Date 2004-11
Est. Completion 2007-04
Phase Phase 1

Sponsor

Allergan

314 total trials

What the Registry Record Tells You About NCT00363714

The ClinicalTrials.gov registry entry for NCT00363714 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 26 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Allergan, which has 314 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which AGN211745 is the first listed.

NCT00363714 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00363714 about?

NCT00363714 is a clinical study titled "A Dose Escalation Trial of an Intravitreal Injection of Sirna-027 in Patients With Subfoveal Choroidal Neovascularization (CNV) Secondary to Age-Related Macular Degeneration (AMD)". The purpose of this study will be to assess the safety and tolerability and dose-limiting toxicity of a single intravitreal injection of Sirna-027 (AGN211745) and to assess the anatomical changes in the retina, changes in CNV, and changes in visual acuity. Escalation to the next dose cohort will be ...

What is the current status of trial NCT00363714?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 26 participants. The study started on 2004-11. Estimated completion is 2007-04.

What interventions are being tested in trial NCT00363714?

The interventions under investigation include: AGN211745 (DRUG).

Who is sponsoring clinical trial NCT00363714?

This trial is sponsored by Allergan, which has 314 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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.