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NCT00705939 · ClinicalTrials.gov registry record · Phase 3

Plant Cell Expressed Recombinant Human Glucocerebrosidase Extension Trial

A Phase 3 study, sponsored by Pfizer.

Completed
Registry status
Phase 3
Development phase
45
Enrollment target

NCT00705939: Completed Phase 3 study, sponsored by Pfizer.

NCT00705939 is a Phase 3 study that has completed, run by Pfizer. The registered enrollment target is 45 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00705939, a Phase 3 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 3
Development phase
45 participants
Enrollment target

Study Summary

Gaucher disease, the most prevalent lysosomal storage disorder, is caused by mutations in the human glucocerebrosidase gene (GCD) leading to reduced activity of the lysosomal enzyme glucocerebrosidase and thereby to the accumulation of substrate glucocerebroside (GlcCer) in the cells of the monocyte-macrophage system. This is an extension trial to Study NCT00376168 and NCT00712348.

Primary Outcome

Spleen volume measured by MRI

Interventions

  • DRUG Taliglucerase alfa

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2008-06
Est. Completion 2013-08
Phase Phase 3
Pfizer

1,845 total trials

What the finished NCT00705939 record still lists

NCT00705939 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 45 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (94% lower).

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

NCT00705939 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00705939 about?

NCT00705939 is a clinical study titled "Plant Cell Expressed Recombinant Human Glucocerebrosidase Extension Trial". Gaucher disease, the most prevalent lysosomal storage disorder, is caused by mutations in the human glucocerebrosidase gene (GCD) leading to reduced activity of the lysosomal enzyme glucocerebrosidase and thereby to the accumulation of substrate glucocerebroside (GlcCer) in the cells of the monocyte...

What is the current status of trial NCT00705939?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 45 participants. The study started on 2008-06. Estimated completion is 2013-08.

What interventions are being tested in trial NCT00705939?

The interventions under investigation include: Taliglucerase alfa (DRUG).

Who is sponsoring clinical trial NCT00705939?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00705939's enrollment target sits among peer trials

45 1870th of 2000 higher than 127 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT00705939, the US trial registry maintained by the National Library of Medicine. NCT00705939 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.