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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00004293
Other study ID # 199/11725
Secondary ID UPITTS-M1230
Status Recruiting
Phase Phase 2
First received October 18, 1999
Last updated June 23, 2005
Start date November 1999

Study information

Verified date December 2003
Source National Center for Research Resources (NCRR)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

OBJECTIVES:

I. Evaluate the efficacy and toxicity of glucocerebrosidase enzyme therapy in patients with Gaucher disease.


Description:

PROTOCOL OUTLINE:

Patients are treated with intravenous glucocerebrosidase every 2 weeks. The dose is based on clinical severity of disease and response to therapy.


Recruitment information / eligibility

Status Recruiting
Enrollment 24
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility PROTOCOL ENTRY CRITERIA:

--Disease Characteristics-- Gaucher disease with glucocerebrosidase deficiency confirmed by enzymatic or molecular assay At least 3 organ systems affected, based on the following criteria: Anemia Thrombocytopenia Organomegaly Bone deterioration on radiograph Pulmonary compromise Symptoms compromise daily activities or risk longevity No neurologic disease

Study Design

Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
glucocerebrosidase


Locations

Country Name City State
United States University of Pittsburgh Pittsburgh Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
National Center for Research Resources (NCRR) University of Pittsburgh

Country where clinical trial is conducted

United States, 

See also
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