Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED Phase 3

Switchover Trial From Imiglucerase to Plant Cell Expressed Recombinant Human Glucocerebrosidase

NCT00712348 · View on ClinicalTrials.gov ↗

Study Summary

This is a multi-center, open-label, switchover trial to assess the safety of taliglucerase alfa in 30 patients with Gaucher disease who are currently being treated with imiglucerase (Cerezyme®) enzyme replacement therapy.

Conditions Studied

Interventions

  • DRUG Taliglucerase alfa

Study Locations (10)

Other

  • Rambam Medical Center — Haifa
  • Shaare Zedek Medical Center — Jerusalem
  • Sala de Hematologia, Hospital Universitario Miguel Servet — Zaragoza
  • Lysosomal Disorders Service, Addenbrookes Hospital NHS Trust — Cambridge
  • Royal Free Hospital — London

Florida

  • University Research Foundation for Lysosomal Storage Diseases, Inc. — Coral Springs

Georgia

  • Department of Human Genetics, Emory University School of Medicine — Decatur

New York

  • Neurogenetics, NYU at Rivergate — New York

Victoria

  • Bone Marrow Transplant Service, The Royal Melbourne Hospital — Parkville

Ontario

  • Mount Sinai Hospital — Toronto

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2008-12
Est. Completion 2013-05
Phase Phase 3

Sponsor

Pfizer

769 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00712348

The ClinicalTrials.gov registry entry for NCT00712348 describes a study currently listed as completed. It is categorized as Phase 3, 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 31 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 769 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 Gaucher Disease appearing as the primary indexed condition, and to 1 intervention — of which Taliglucerase alfa 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: NCT00712348 reports 10 study locations spanning 6 distinct geographic areas — top geographies include Other, Florida, Georgia. 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 NCT00712348 about?

NCT00712348 is a clinical study titled "Switchover Trial From Imiglucerase to Plant Cell Expressed Recombinant Human Glucocerebrosidase". This is a multi-center, open-label, switchover trial to assess the safety of taliglucerase alfa in 30 patients with Gaucher disease who are currently being treated with imiglucerase (Cerezyme®) enzyme replacement therapy.

What is the current status of trial NCT00712348?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 31 participants. The study started on 2008-12. Estimated completion is 2013-05.

What conditions does trial NCT00712348 study?

This clinical trial studies the following conditions: Gaucher Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00712348?

The interventions under investigation include: Taliglucerase alfa (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00712348?

This trial is sponsored by Pfizer, which has 769 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00712348 being conducted?

This trial has 10 study locations across Florida, Georgia, New York, Victoria, Ontario. 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