A Multicenter, Safety and Efficacy Study of Taliglucerase Alfa in Subjects With Type 3 Gaucher Disease

NCT ID: NCT04002830

Last Updated: 2024-12-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 14 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-11-20
• Study Completion Date: 2023-07-30

Brief Summary

This is a multicenter study to assess the safety and efficacy of taliglucerase alfa (60 units/kg) in previously untreated subjects of any age with Type 3 GD. Subjects will receive an infusion of taliglucerase alfa every 2 weeks for 12 months. Subjects who tolerate the infusions well, and who are treated in centers where home therapy is the SOC will be allowed to switch from site to home treatment at the discretion of the PI but after no less than 3 uneventful infusions at the site.

Detailed Description

Patients with Type 3 GD exhibit both visceral and neurologic manifestations. In addition to the progressive neurologic involvement, somatic disease manifestations, especially splenomegaly and resulting cytopenia, contribute to significant mortality and morbidity . The effects of enzyme replacement therapy (ERT) on patients with Type 1 GD have been clearly documented and have a beneficial effect on visceral and hematologic disease parameters . It is known that recombinant enzyme does not pass the blood-brain barrier and has no effect on neurologic involvement . Probably due to the rarity of Type 3 GD, information on the somatic effects of ERT is largely limited to case reports or single-center series. There are also few reviews of cohorts but the clinical subtype, age, genotype, ERT dosage, accompanying therapies, and treatment response vary widely among patients in these cohorts. This prospective study aims to objectively evaluate the hematologic and visceral effects of ERT with taliglucerase alfa on a rather clinically and genetically homogenous group of treatment-naïve patients with Type 3 GD . For the purposes of this study, subjects receiving no Gaucher-specific medications for at least 12 months will be considered "untreated". The results of this study are expected to provide a more objective view of the degree of response of this patient type, and potentially create new areas of research.

Conditions

Gaucher Disease, Type 3

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Taliglucerase Alpha

Intravenous infusion of Taligluucerase alfa (Elelyso) in treatment-naive patients with type 3 Gaucher disease

Group Type: EXPERIMENTAL

Elelyso

Intervention Type: DRUG

Taliglucerase alfa is currently an approved therapy in the United States and many other countries for adults and children with a confirmed diagnosis of Type 1 GD ,and is also approved for use in Type 3 GD in a small number of countries.

Interventions

Elelyso

Taliglucerase alfa is currently an approved therapy in the United States and many other countries for adults and children with a confirmed diagnosis of Type 1 GD ,and is also approved for use in Type 3 GD in a small number of countries.

Intervention Type: DRUG

Other Intervention Names

Taliglucerase Alfa

Eligibility Criteria

Inclusion Criteria

1. Male or female of any age; however, if female:

• must be using contraception if of childbearing potential or must be surgically sterile
• must not be lactating

2. Diagnosis of Type 3 GD by enzyme and sequence analysis; and confirmed by the Medical Monitor.

3. Splenomegaly at least 5 x multiples of normal (MN).

4. Treatment-naïve.

Exclusion Criteria

1. Type 2 GD.

2. Presence of myoclonic seizures.

3. At least one allele of:

• N370S (N409S in recent nomenclature)
• R496H (R535H in recent nomenclature)

4. Presence of calcification in heart valves or arteries in echocardiography.

5. Presence of untreated iron, folic acid, vitamin B12 deficiency and/or hypothyroidism. (Resolved anemia is not an exclusion criterion.)

6. Presence of human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), and/or hepatitis C infections.

7. Splenectomy and bone marrow transplantation.

8. Presence of any medical, emotional, behavioural, or psychological condition that in the judgment of the Investigator would interfere with the subject's compliance with the requirements of the study.

9. Any other disorder that may interfere with the results of the efficacy endpoints.

10. Pregnancy or breastfeeding.

11. Currently taking another investigational drug for any condition or any therapeutic drug for Gaucher disease.

12. The subject and/or subject's parent(s) or legal guardian(s) are unable to understand the nature, scope, and possible consequences of the study.

13. Medical history of any food/drugs allergy.

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Pfizer

INDUSTRY

Sponsor Role: collaborator

Ari Zimran

OTHER

Sponsor Role: lead

Responsible Party

Ari Zimran

PI

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Ari Zimran, Prof.

Role: PRINCIPAL_INVESTIGATOR

Shaare Zedek Medical Center

Locations

All India Institute of Medical Sciences

New Delhi, , India

Shaare Zedek Medical Center

Jerusalem, , Israel

Gazi University

Ankara, , Turkey (Türkiye)

Countries

India; Israel; Turkey (Türkiye)

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

WI224302

Identifier Type: -

Identifier Source: org_study_id