Study of Velaglucerase Alfa Enzyme Replacement Therapy in Japanese Patients With Gaucher Disease

Gaucher Disease Clinical Trial

Official title:

A Multicenter, Open-Label Study of Velaglucerase Alfa Enzyme Replacement Therapy in Japanese Patients With Gaucher Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01614574
• Other study ID #: HGT-GCB-087
• Status: Completed
• Phase: Phase 3
• Start date: March 2, 2012
• Est. completion date: May 25, 2013

Study information

• Verified date: June 2021
• Source: Takeda
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Gaucher disease is an inherited deficiency of the lysosomal enzyme glucocerebrosidase (GCB) that leads to progressive accumulation of glucocerebroside within macrophages and subsequent tissue and organ damage; typically of the liver, spleen, bone marrow, and brain. The disease has been classified into 3 clinical subtypes based on the presence or absence of neurological symptoms and severity of neurological disease. Type 1 Gaucher disease affects an estimated 30,000 persons worldwide and is the most common. Type 1 Gaucher disease does not involve the central nervous system. Patients with type 2 Gaucher disease present with acute neurological deterioration, which leads to early death. Those with type 3 disease typically display a more sub-acute neurological course, with later onset and slower progression.

The primary objective of this study is to evaluate the safety of every other week dosing of velaglucerase alfa in Japanese patients with Gaucher disease.

Velaglucerase alfa has been developed and approved as an enzyme replacement therapy for Type 1 Gaucher disease.

Description:

Gaucher disease is an inherited deficiency of the lysosomal enzyme glucocerebrosidase (GCB) that leads to progressive accumulation of glucocerebroside within macrophages and subsequent tissue and organ damage; typically of the liver, spleen, bone marrow, and brain.

Gaucher disease has been designated in the list of Specified Rare and Intractable Diseases by Specified Disease Treatment Research Program of Ministry of Health, Labor and Welfare (MHLW) as one of "lysosomal storage diseases" since 2001. Gaucher disease is also designated in the Medical Aid Program for Specified Categories of Chronic Pediatric Diseases.

The prevalence of mutations and the phenotype of patients with Gaucher disease in Japan differs from that in non-Japanese populations. Some patients with type 1 Gaucher disease in Japan have more severe and progressive disease compared to non-Japanese patients and the disease is characterized by an earlier onset of symptoms.

Velaglucerase alfa, a highly-purified form of the naturally occurring enzyme glucocerebrosidase, has been developed as an enzyme replacement therapy for Gaucher disease for the symptoms (anemia, thrombocytopenia, hepatomegaly, splenomegaly, and bone manifestation).

The primary objective of this study is to evaluate the safety of every other week dosing of velaglucerase alfa in Japanese patients (naive or previously treated with imiglucerase) 2 years of age and older with Gaucher disease.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 6
• Est. completion date: May 25, 2013
• Est. primary completion date: May 25, 2013
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Years and older

Eligibility

Inclusion Criteria:

• The patient has a documented diagnosis of Gaucher disease

• The patient is at least 2 years of age

• Female patients of child bearing potential must agree to use a medically acceptable method of contraception at all times during the study

• The patient, the patient's parent(s) or legal guardian(s) has provided written informed consent that has been approved by the Institutional Review Board/Independent Ethics Committee (IRB/IEC)

• The patient must be sufficiently cooperative to participate in this clinical study as judged by the Investigator

Patients who are switched from imiglucerase ERT must meet the following additional criteria:

• Received treatment with imiglucerase for a minimum of 12 consecutive months

• Meet predefined limits for hemoglobin concentration and platelet counts

Patients naïve to treatment for Gaucher disease must meet the following additional criteria:

• Not received treatment for Gaucher disease (investigational or approved products) within 12 months prior to study entry

• Have Gaucher disease related anemia and at least one of the following: moderate splenomegaly or, Gaucher disease-related thrombocytopenia or Gaucher disease-related enlarged liver

Exclusion Criteria:

• Treatment with any investigational drug or device within the 30 days prior to study entry (time of informed consent); such use during the study is not permitted

• Positive for hepatitis B or hepatitis C.

• Non-Gaucher disease related anemia

• The patient, patient's parent(s), or patient's legal guardian(s) is/are unable to understand the nature, scope, and possible consequences of the study

• Significant comorbidity, as determined by the Investigator that might affect study data or confound the study results

• The patient is unable to comply with the protocol or is unlikely to complete the study, as determined by the Investigator

• The patient has experienced a severe (grade 3 or higher) infusion-related hypersensitivity reaction (anaphylactic or anaphylactoid reaction) to any ERT (approved or investigational)

• Currently receiving red blood cell growth factor, (eg, erythropoietin) or chronic systemic corticosteroids in the last 6 months

• Patient has had a splenectomy or the patient has an active, clinically significant spleen infarction within 12 months of screening

• Patient has worsening bone necrosis within 12 months of screening

• The patient is pregnant or lactating.

Related Conditions & MeSH terms

• Gaucher Disease

Intervention

Biological:
• velaglucerase alfa
60 U/kg every other week intravenous infusion

Locations

Country	Name	City	State
Japan	Hamamatsu University School of Medicine	Hamamatsu	Shizuoka
Japan	The Jikei University School of Medicine	Minato-ku	Toyko
Japan	Osaka City University Hospital	Osaka

Sponsors (1)

Lead Sponsor	Collaborator
Shire

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Severe Adverse Events (SAE)		Baseline to week 51
Primary	Number of Treatment Emergent Adverse Events (TEAE)		Baseline to week 51
Primary	Development of Anti-velaglucerase Alfa Antibody		Baseline to week51
Primary	Number of Infusion- Related Adverse Events		Baseline to week 51
Primary	Number of Patients With Concomitant Medication		Baseline to week 51
Secondary	Change From Baseline in Hemoglobin Concentration		Baseline to week 51
Secondary	Change From Baseline in Platelet Count		Baseline to week 51
Secondary	Change From Baseline in Liver Volume, Normalized to Body Weight		Baseline to week 51
Secondary	Change From Baseline in Spleen Volume, Normalized to Body Weight		Baseline to week 51
Secondary	Change From Baseline in Plasma Chitotriosidase Levels		Baseline to week 51
Secondary	Change From Baseline in CCL18 Levels		Baseline to week 51