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Efficacy and Safety Study of GB-0998 for Treatment of Steroid-resistant Polymyositis and Dermatomyositis (PM/DM)

Primary Purpose

Polymyositis, Dermatomyositis

Status
Completed
Phase
Phase 3
Locations
Japan
Study Type
Interventional
Intervention
GB-0998
Placebo of GB-0998
Sponsored by
Japan Blood Products Organization
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Polymyositis focused on measuring polymyositis, dermatomyositis, High-dose intravenous immunoglobulin, Venoglobulin-IH, Steroid-resistant polymyositis(PM) and dermatomyositis(DM)

Eligibility Criteria

16 Years - 75 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients who have been defined as "definite" based on the criteria of Bohan and Peter for polymyositis and dermatomyositis. Patients who are defined as steroid-resistant ones based on the changes of scores on manual muscle testing (MMT) and serum levels of creatine kinase (CK) during observation period before administration of drug. Exclusion Criteria: Patients with malignant tumors. Patients with acute interstitial pneumonia, including acute exacerbation of chronic. Patients with severe muscular atrophy for a long period. Patients with severe infectious disease. Patients who have the anamnesis of shock or hypersensitivity to this drug. Patients with severe hepatic disorder or severe renal disorder. Patients who have the anamnesis of cerebral infarction or ischemic heart disease, or who having symptom of these diseases. Patients who have been diagnosed as IgA deficiency in their past history. Pregnant, lactating, and probably pregnant patients, and patients who want to become pregnant. Patients who were administered immunoglobulin dosage within 6 weeks before consent.

Sites / Locations

  • Tokyo Medical and Dental University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

Outcomes

Primary Outcome Measures

Changes in manual muscle strength (MMT) scores

Secondary Outcome Measures

Changes in the serum levels of creatine kinase (CK) and total scores of activities of daily living (ADL)
Adverse events and laboratory tests

Full Information

First Posted
June 8, 2006
Last Updated
November 3, 2014
Sponsor
Japan Blood Products Organization
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1. Study Identification

Unique Protocol Identification Number
NCT00335985
Brief Title
Efficacy and Safety Study of GB-0998 for Treatment of Steroid-resistant Polymyositis and Dermatomyositis (PM/DM)
Official Title
A Randomized, Double-blind, Controlled Clinical Study of GB-0998 for the Steroid-resistant Polymyositis and Dermatomyositis
Study Type
Interventional

2. Study Status

Record Verification Date
February 2012
Overall Recruitment Status
Completed
Study Start Date
June 2006 (undefined)
Primary Completion Date
March 2009 (Actual)
Study Completion Date
March 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Japan Blood Products Organization

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This randomized, double-blind, placebo-controlled trial will carry out to assess the efficacy of GB-0998 in the treatment of the steroid-resistant polymyositis and dermatomyositis based on the changes in manual muscle strength (MMT) scores as primary endpoint, and in addition, to assess the safety of GB-0998.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polymyositis, Dermatomyositis
Keywords
polymyositis, dermatomyositis, High-dose intravenous immunoglobulin, Venoglobulin-IH, Steroid-resistant polymyositis(PM) and dermatomyositis(DM)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Title
2
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
GB-0998
Other Intervention Name(s)
High-dose intravenous immunoglobulin, Venoglobulin-IH
Intervention Description
8 mL (400 mg of GB-0998)/kg per day is intravenously administered for five successive days
Intervention Type
Drug
Intervention Name(s)
Placebo of GB-0998
Intervention Description
8 mL/kg per day is intravenously administered for five successive days
Primary Outcome Measure Information:
Title
Changes in manual muscle strength (MMT) scores
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Changes in the serum levels of creatine kinase (CK) and total scores of activities of daily living (ADL)
Time Frame
8 weeks
Title
Adverse events and laboratory tests
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients who have been defined as "definite" based on the criteria of Bohan and Peter for polymyositis and dermatomyositis. Patients who are defined as steroid-resistant ones based on the changes of scores on manual muscle testing (MMT) and serum levels of creatine kinase (CK) during observation period before administration of drug. Exclusion Criteria: Patients with malignant tumors. Patients with acute interstitial pneumonia, including acute exacerbation of chronic. Patients with severe muscular atrophy for a long period. Patients with severe infectious disease. Patients who have the anamnesis of shock or hypersensitivity to this drug. Patients with severe hepatic disorder or severe renal disorder. Patients who have the anamnesis of cerebral infarction or ischemic heart disease, or who having symptom of these diseases. Patients who have been diagnosed as IgA deficiency in their past history. Pregnant, lactating, and probably pregnant patients, and patients who want to become pregnant. Patients who were administered immunoglobulin dosage within 6 weeks before consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nobuyuki Miyasaka, Professor
Organizational Affiliation
Tokyo Medical and Dental University
Official's Role
Study Chair
Facility Information:
Facility Name
Tokyo Medical and Dental University
City
Bunkyo-ku
State/Province
Tokyo
ZIP/Postal Code
113-8519
Country
Japan

12. IPD Sharing Statement

Learn more about this trial

Efficacy and Safety Study of GB-0998 for Treatment of Steroid-resistant Polymyositis and Dermatomyositis (PM/DM)

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