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NCT00713518 · ClinicalTrials.gov registry record · Phase 2

Phase II Open Label Multicenter Study For Age Related Macular Degeneration Comparing PF-04523655 Versus Lucentis In The Treatment Of Subjects With CNV (MONET Study).

A Phase 2 study, sponsored by Quark Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
152
Enrollment target

NCT00713518: Completed Phase 2 study, sponsored by Quark Pharmaceuticals.

NCT00713518 is a Phase 2 study that has completed, run by Quark Pharmaceuticals. The registered enrollment target is 152 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (14% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00713518, a Phase 2 study, has completed, sponsored by Quark Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
152 participants
Enrollment target

Study Summary

The aim of the study is to evaluate whether PF-04523655 is effective in the treatment of neovascular/wet AMD and at which dose.

Interventions

  • DRUG 0.5 mg ranibizumab
  • DRUG 3 mg PF-04523655
  • DRUG 1 mg PF-04523655

Trial Details

FieldValue
Enrollment Target 152 participants
Start Date 2009-11
Est. Completion 2011-07
Phase Phase 2
Quark Pharmaceuticals

14 total trials

What the finished NCT00713518 record still lists

NCT00713518 is an interventional study that assigns participants to a tested intervention. The registered 152 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (14% higher).

The record links to 0 conditions, and to 3 interventions - of which 0.5 mg ranibizumab is the first listed.

NCT00713518 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00713518 about?

NCT00713518 is a clinical study titled "Phase II Open Label Multicenter Study For Age Related Macular Degeneration Comparing PF-04523655 Versus Lucentis In The Treatment Of Subjects With CNV (MONET Study).". The aim of the study is to evaluate whether PF-04523655 is effective in the treatment of neovascular/wet AMD and at which dose.

What is the current status of trial NCT00713518?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 152 participants. The study started on 2009-11. Estimated completion is 2011-07.

What interventions are being tested in trial NCT00713518?

The interventions under investigation include: 0.5 mg ranibizumab (DRUG), 3 mg PF-04523655 (DRUG), 1 mg PF-04523655 (DRUG).

Who is sponsoring clinical trial NCT00713518?

This trial is sponsored by Quark Pharmaceuticals, which has 14 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00713518's enrollment target sits among peer trials

152 452nd of 2000 higher than 1,547 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 NCT00713518, the US trial registry maintained by the National Library of Medicine. NCT00713518 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.