A Study of MDX-1100 in Subjects With Active Ulcerative Colitis (MDX1100-06)
Primary Purpose
Ulcerative Colitis
Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
sterile saline for injection
MDX-1100
Sponsored by
About this trial
This is an interventional treatment trial for Ulcerative Colitis focused on measuring ulcerative colitis, rectal bleeding
Eligibility Criteria
Inclusion Criteria:
- Subjects with active UC on either 5-ASA,corticosteroids,azathioprine(AZA) and or/6-mercaptopurine(6-MP);
- Mayo score of 6 to 10 points with moderate to severe disease on endoscopy
Subjects on the following medications;
- prednisolone ≤ 20 mg daily (or equivalent) (dose must be stable for at least 2 weeks prior to study drug administration)
- 5-ASA (dose must be stable for at least 4 weeks prior to study drug administration)
- AZA or 6-MP (dose must be stable for at least 3 months prior to study drug administration)
- Rectal steroids or 5-ASA (must have been stable for at least 4 weeks prior to study drug)
Exclusion Criteria:
- Anti-TNF therapy within 8 weeks before study drug administration
- Contraindication to colonoscopy or sigmoidoscopy
- Primary or secondary immunodeficiency
- Autoimmune disease besides UC, with the exceptions of Sjogren's syndrome or hypothyroidism
- History of malignancy, excluding adequately treated and cured basal or squamous cell of the skin, or cervical carcinoma in situ
- Evidence of acute or chronic infection
- Clinically significant disease requiring medication
Sites / Locations
- Advanced Medical Research Center
- Florida Medical Clinic-Tampa Clinic
- Northwestern University Feinberg School of Medicine
- Chevy Chase Clinical Research
- Washington University School of Medicine
- Mount Sinai School of Medicine
- Dayton Science Institute
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
2
1
Arm Description
sterile saline for injection
MDX-1100 for injection
Outcomes
Primary Outcome Measures
Change in Mayo score at Day 57 compared with Screening
Secondary Outcome Measures
the remission rate
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00656890
Brief Title
A Study of MDX-1100 in Subjects With Active Ulcerative Colitis
Acronym
MDX1100-06
Official Title
A Phase 2, Multi-dose, Double-blind, Placebo-controlled, Randomized, Multicenter Study of MDX-1100 (Anti-CXCL10 Human Monoclonal Antibody) in Subjects With Active Ulcerative Colitis
Study Type
Interventional
2. Study Status
Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
April 2008 (undefined)
Primary Completion Date
September 2009 (Actual)
Study Completion Date
September 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bristol-Myers Squibb
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine the safety and tolerability of the MDX-1100 regimen in subjects with active Ulcerative colitis(UC) and determine the response rate at day 57 in patients administered MDX-1100.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis
Keywords
ulcerative colitis, rectal bleeding
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
110 (Actual)
8. Arms, Groups, and Interventions
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
sterile saline for injection
Arm Title
1
Arm Type
Experimental
Arm Description
MDX-1100 for injection
Intervention Type
Biological
Intervention Name(s)
sterile saline for injection
Intervention Description
10mg/kg/dose sterile saline injected every other week for a total of 4 doses
Intervention Type
Biological
Intervention Name(s)
MDX-1100
Intervention Description
10mg/kg/dose MDX-1100 injected every other week for a total of 4 doses
Primary Outcome Measure Information:
Title
Change in Mayo score at Day 57 compared with Screening
Time Frame
Day 57
Secondary Outcome Measure Information:
Title
the remission rate
Time Frame
Day 57
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subjects with active UC on either 5-ASA,corticosteroids,azathioprine(AZA) and or/6-mercaptopurine(6-MP);
Mayo score of 6 to 10 points with moderate to severe disease on endoscopy
Subjects on the following medications;
prednisolone ≤ 20 mg daily (or equivalent) (dose must be stable for at least 2 weeks prior to study drug administration)
5-ASA (dose must be stable for at least 4 weeks prior to study drug administration)
AZA or 6-MP (dose must be stable for at least 3 months prior to study drug administration)
Rectal steroids or 5-ASA (must have been stable for at least 4 weeks prior to study drug)
Exclusion Criteria:
Anti-TNF therapy within 8 weeks before study drug administration
Contraindication to colonoscopy or sigmoidoscopy
Primary or secondary immunodeficiency
Autoimmune disease besides UC, with the exceptions of Sjogren's syndrome or hypothyroidism
History of malignancy, excluding adequately treated and cured basal or squamous cell of the skin, or cervical carcinoma in situ
Evidence of acute or chronic infection
Clinically significant disease requiring medication
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bristol-Myers Squibb
Organizational Affiliation
Bristol-Myers Squibb
Official's Role
Study Director
Facility Information:
Facility Name
Advanced Medical Research Center
City
Port Orange
State/Province
Florida
ZIP/Postal Code
32127
Country
United States
Facility Name
Florida Medical Clinic-Tampa Clinic
City
Tampa
State/Province
Florida
ZIP/Postal Code
33613
Country
United States
Facility Name
Northwestern University Feinberg School of Medicine
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
Chevy Chase Clinical Research
City
Chevy Chase
State/Province
Maryland
ZIP/Postal Code
20815
Country
United States
Facility Name
Washington University School of Medicine
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Facility Name
Mount Sinai School of Medicine
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States
Facility Name
Dayton Science Institute
City
Dayton
State/Province
Ohio
ZIP/Postal Code
45415
Country
United States
City
Abbotsford
State/Province
British Columbia
ZIP/Postal Code
V2S 3N5
Country
Canada
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 1H2
Country
Canada
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M3N 2V7
Country
Canada
City
Olomouc
Country
Czech Republic
City
Prague
Country
Czech Republic
City
Strakonice
Country
Czech Republic
City
Tabor
Country
Czech Republic
City
Usti nad Labem
Country
Czech Republic
City
Valasske Mezifici
Country
Czech Republic
City
Budapest
Country
Hungary
City
Debrecen
Country
Hungary
City
Gyula
Country
Hungary
City
Kaposvar
Country
Hungary
City
Kecskemet
Country
Hungary
City
Nagykanizsa
Country
Hungary
City
Siofok
Country
Hungary
City
Vac
Country
Hungary
City
Zalaegerszeg
Country
Hungary
City
Daugavpils
Country
Latvia
City
Riga
Country
Latvia
City
Valmiera
Country
Latvia
City
Bucharest
Country
Romania
City
Cluj
Country
Romania
City
Oradea
Country
Romania
City
Tg. Mures
Country
Romania
City
Timisoara
Country
Romania
City
Moscow
Country
Russian Federation
City
Saratov
Country
Russian Federation
City
Yaroslavl
Country
Russian Federation
City
Chernivtsy
Country
Ukraine
City
Dniepropetrovsk
Country
Ukraine
City
Donetsk
Country
Ukraine
City
Kharkiv
Country
Ukraine
City
Kharkov
Country
Ukraine
City
Kiev
Country
Ukraine
City
Kyiv
Country
Ukraine
City
Lviv
Country
Ukraine
City
Simferopol
Country
Ukraine
12. IPD Sharing Statement
Citations:
PubMed Identifier
23461895
Citation
Mayer L, Sandborn WJ, Stepanov Y, Geboes K, Hardi R, Yellin M, Tao X, Xu LA, Salter-Cid L, Gujrathi S, Aranda R, Luo AY. Anti-IP-10 antibody (BMS-936557) for ulcerative colitis: a phase II randomised study. Gut. 2014 Mar;63(3):442-50. doi: 10.1136/gutjnl-2012-303424. Epub 2013 Mar 5.
Results Reference
derived
Learn more about this trial
A Study of MDX-1100 in Subjects With Active Ulcerative Colitis
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