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NCT01229215 · ClinicalTrials.gov registry record · Phase 2

A Study of Safety, Tolerability, and Evidence of Activity of FCFD4514S Administered Monthly or Every Other Month to Patients With Geographic Atrophy

A Phase 2 study, sponsored by Genentech.

Completed
Registry status
Phase 2
Development phase
143
Enrollment target

NCT01229215: Completed Phase 2 study, sponsored by Genentech.

NCT01229215 is a Phase 2 study that has completed, run by Genentech. The registered enrollment target is 143 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01229215, a Phase 2 study, has completed, sponsored by Genentech.

COMPLETED
Registry status
Phase 2
Development phase
143 participants
Enrollment target

Study Summary

This is a Phase Ib/II, multicenter, randomized, single-masked, sham-injection-controlled study of safety, tolerability, and evidence of activity of FCFD4514S intravitreal injections administered monthly or every other month in patients with geographic atrophy.

Interventions

  • DRUG FCFD4514S
  • DRUG sham

Trial Details

FieldValue
Enrollment Target 143 participants
Start Date 2011-02
Est. Completion 2013-04
Phase Phase 2
Genentech

332 total trials

What the finished NCT01229215 record still lists

NCT01229215 is an interventional study that assigns participants to a tested intervention. The registered 143 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

The record links to 0 conditions, and to 2 interventions - of which FCFD4514S is the first listed.

NCT01229215 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01229215 about?

NCT01229215 is a clinical study titled "A Study of Safety, Tolerability, and Evidence of Activity of FCFD4514S Administered Monthly or Every Other Month to Patients With Geographic Atrophy". This is a Phase Ib/II, multicenter, randomized, single-masked, sham-injection-controlled study of safety, tolerability, and evidence of activity of FCFD4514S intravitreal injections administered monthly or every other month in patients with geographic atrophy.

What is the current status of trial NCT01229215?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 143 participants. The study started on 2011-02. Estimated completion is 2013-04.

What interventions are being tested in trial NCT01229215?

The interventions under investigation include: FCFD4514S (DRUG), sham (DRUG).

Who is sponsoring clinical trial NCT01229215?

This trial is sponsored by Genentech, which has 332 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01229215's enrollment target sits among peer trials

143 507th of 2000 higher than 1,494 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 NCT01229215, the US trial registry maintained by the National Library of Medicine. NCT01229215 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.