Safety of RG2077 in Patients With Multiple Sclerosis
Primary Purpose
Multiple Sclerosis, Multiple Sclerosis, Relapsing-Remitting
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
RG2077 (CTLA4-IgG4m)
Sponsored by
About this trial
This is an interventional treatment trial for Multiple Sclerosis focused on measuring Ataxia, MRI, MS, CTLA4-IgG4m, Costimulatory Signals, Autoimmune Disorders
Eligibility Criteria
Inclusion Criteria Confirmed diagnosis of MS, defined as an MRI consistent with MS plus two separate clinical events, or one clinical event and MRI consistent with demyelination plus a second MRI demonstrating new lesions Have declined all FDA approved therapies for MS
Sites / Locations
- Brigham and Women's Hospital/Harvard Medical School
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Experimental
Experimental
Arm Label
1
2
3
4
Arm Description
Participants receive Regimen 1 for 4 months
Participants receive Regimen 2 for 4 months
Participants receive Regimen 3 for 4 months
Participants receive Regimen 4 for 4 months
Outcomes
Primary Outcome Measures
Safety assessment including a MRI, neurological and physical examinations
Secondary Outcome Measures
Number of gadolinium (GD) enhancing lesions and T2 lesion volume on MRI
Full Information
NCT ID
NCT00076934
First Posted
February 6, 2004
Last Updated
March 23, 2017
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Immune Tolerance Network (ITN), Repligen Corporation
1. Study Identification
Unique Protocol Identification Number
NCT00076934
Brief Title
Safety of RG2077 in Patients With Multiple Sclerosis
Official Title
A Phase I Study: Safety of RG2077 (CTLA4-IgG4m) in Patients With Relapsing-Remitting Multiple Sclerosis
Study Type
Interventional
2. Study Status
Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
January 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
February 2006 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Immune Tolerance Network (ITN), Repligen Corporation
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Multiple sclerosis (MS) is an autoimmune disorder. In this disease, the body's immune system attacks and destroys the cells that cover and protect nerves. This study will test the safety of a new drug called RG2077 that is designed to treat MS. The study will not determine whether RG2077 is effective in treating MS, only whether it is safe to use in patients with MS.
Study hypothesis: RG2077 will arrest MS if administered early in the course of MS and decrease accumulation of lesions on MRI.
Detailed Description
Effective treatment of autoimmune disorders is likely to arise not from improved immunosuppression, but from improved understanding of the normal mechanisms that generate and maintain self-tolerance. RG2077 may block a T cell costimulation pathway central to the pathophysiology of MS. A total of 20 patients with MS will be enrolled in this study. Each patient participates in the study for 4 months.
The dose-escalation portion of this study evaluated the safety of a single infusion of RG2077 (CTLA4-IgG4m) in 16 patients with MS and is now complete. Patients who participated in the single infusion portion of the study were assigned to one of four groups. Each group received a different dose of RG2077. The second portion of the study will evaluate the safety of 4 doses of RG2077 in 4 additional patients. In the multiple infusion portion of the study, all patients will receive the same dose of RG2077. Patients will be monitored for possible side effects of RG2077.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis, Multiple Sclerosis, Relapsing-Remitting
Keywords
Ataxia, MRI, MS, CTLA4-IgG4m, Costimulatory Signals, Autoimmune Disorders
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Participants receive Regimen 1 for 4 months
Arm Title
2
Arm Type
Experimental
Arm Description
Participants receive Regimen 2 for 4 months
Arm Title
3
Arm Type
Experimental
Arm Description
Participants receive Regimen 3 for 4 months
Arm Title
4
Arm Type
Experimental
Arm Description
Participants receive Regimen 4 for 4 months
Intervention Type
Drug
Intervention Name(s)
RG2077 (CTLA4-IgG4m)
Intervention Description
RG2077
Primary Outcome Measure Information:
Title
Safety assessment including a MRI, neurological and physical examinations
Time Frame
Throughout study
Secondary Outcome Measure Information:
Title
Number of gadolinium (GD) enhancing lesions and T2 lesion volume on MRI
Time Frame
Throughout study
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria
Confirmed diagnosis of MS, defined as an MRI consistent with MS plus two separate clinical events, or one clinical event and MRI consistent with demyelination plus a second MRI demonstrating new lesions
Have declined all FDA approved therapies for MS
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Samia J. Khoury, MD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brigham and Women's Hospital/Harvard Medical School
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Participant level data and additional relevant materials are available to the public in: 1.) the Immunology Database and Analysis Portal (ImmPort), a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts; and 2.) TrialShare, the Immune Tolerance Network (ITN) Clinical Trials Research Portal.
Citations:
PubMed Identifier
18794494
Citation
Viglietta V, Bourcier K, Buckle GJ, Healy B, Weiner HL, Hafler DA, Egorova S, Guttmann CR, Rusche JR, Khoury SJ. CTLA4Ig treatment in patients with multiple sclerosis: an open-label, phase 1 clinical trial. Neurology. 2008 Sep 16;71(12):917-24. doi: 10.1212/01.wnl.0000325915.00112.61.
Results Reference
result
Links:
URL
https://www.niaid.nih.gov/
Description
National Institute of Allergy and Infectious Diseases (NIAID) website
URL
https://www.niaid.nih.gov/about/dait
Description
Division of Allergy, Immunology, and Transplantation (DAIT) website
URL
http://www.immunetolerance.org
Description
Immune Tolerance Network (ITN) website
Available IPD and Supporting Information:
Available IPD/Information Type
Individual Participant Data Set
Available IPD/Information URL
http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY661
Available IPD/Information Identifier
SDY661
Available IPD/Information Comments
ImmPort study identifier is SDY661
Available IPD/Information Type
Study protocol synopsis, -summary, -design, -adverse events, -medications,-demographics, - lab tests, -files
Available IPD/Information URL
http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY661
Available IPD/Information Identifier
SDY661
Available IPD/Information Comments
ImmPort study identifier is SDY661
Available IPD/Information Type
Individual Participant Data Set
Available IPD/Information URL
http://www.itntrialshare.org/project/Studies/ITN006AIPUBLIC/Study%20Data/begin.view?
Available IPD/Information Identifier
ITN006AI/NMS02
Available IPD/Information Comments
TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available.
Available IPD/Information Type
Study protocol synopsis; -schedule of assessments; data and reports; adverse event(s); -specimens availability; -manuscripts and abstracts
Available IPD/Information URL
http://www.itntrialshare.org/project/Studies/ITN006AIPUBLIC/Study%20Data/begin.view?
Available IPD/Information Identifier
ITN006AI/NMS02
Available IPD/Information Comments
TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available.
Learn more about this trial
Safety of RG2077 in Patients With Multiple Sclerosis
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