Alefacept for Chronic Graft Versus Host Disease
Primary Purpose
Resistant Chronic GVHD
Status
Completed
Phase
Phase 1
Locations
Israel
Study Type
Interventional
Intervention
Alefacept
Sponsored by
About this trial
This is an interventional treatment trial for Resistant Chronic GVHD focused on measuring GVHD
Eligibility Criteria
Inclusion Criteria:
- No age limit
- Resistant chronic GVHD
Exclusion Criteria:
- Not fulfilling any of the inclusion criteria
- Active life-threatening infection
- Inability to comply with study requirements.
- Known hypersensitivity to alefacept.
- Active malignant disease
Sites / Locations
- Department of Stem cell Transplantation & Cancer immunotherapy; Cell Therapy & Transplantation Biology Research Laboratory, Hadassah University Hospital
Outcomes
Primary Outcome Measures
GVHD response.
Time to GVHD response
Secondary Outcome Measures
Overall survival.
Disease free survival.
Occurrence of infections.
Full Information
NCT ID
NCT00397332
First Posted
November 8, 2006
Last Updated
April 19, 2015
Sponsor
Hadassah Medical Organization
1. Study Identification
Unique Protocol Identification Number
NCT00397332
Brief Title
Alefacept for Chronic Graft Versus Host Disease
Official Title
An Investigator Initiated Open-label and Explorative Study of Alefacept Treatment for Chronic Extensive Graft Versus Host Disease
Study Type
Interventional
2. Study Status
Record Verification Date
February 2011
Overall Recruitment Status
Completed
Study Start Date
October 2006 (undefined)
Primary Completion Date
January 2013 (Actual)
Study Completion Date
July 2013 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Hadassah Medical Organization
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Alefacept (AMEVIVE®) is an immunosuppressive dimeric fusion protein that consists of the extracellular CD2-binding portion of the human leukocyte function antigen-3 (LFA-3) linked to the Fcof IgG1. Alefacept is produced by recombinant DNA technology in a Chinese Hamster Ovary (CHO) mammalian cell expression system. It was shown to interfere with lymphocyte activation. Alefacept was evaluated in two randomized, double-blind, placebo-controlled studies in adults with chronic plaque psoriasis. Each course consisted of once-weekly administration for 12 weeks of placebo or alefacept. The response to alefacept was significantly better in both studies. In both studies, onset of response to alefacept treatment (defined as at least 50% reduction of baseline Psoriasis Area and Severity Index (PASI)) began 60 days after the start of therapy. With one course of therapy, the median duration of response (defined as maintenance of a 75% or greater reduction in PASI) was 3.5 months for alefacept treated patients and 1 month for placebo-treated patients. Most patients who had responded to either alefacept or placebo maintained a 50% or greater reduction in PASI through the 3-month observation period.
Graft versus host disease (GVHD) is the most ominous side effect of allogenic stem cell transplantation (SCT). It causes severe inflammatory process, which is usually located to the skin, gut and liver. Treatment of GVHD consists of various immuno-suppressive and immuno-modulating drugs, including steroids, cyclosporine, tacrolimus, methotrexate etc. These drugs unfortunately can also cause severe immunologic failure that makes the patient prone to infection and malignancy, and other medication-specific side effects. In spite of this effect on the immune system, not all of the patients achieve control of GVHD, which usually rapidly leads to death. Despite the use of innovative immunosuppressive modalities, the prognosis of steroid resistant GVHD is usually poor. In the following study we will evaluate the effect of alefacept on steroid unresponsive cGVHD.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Resistant Chronic GVHD
Keywords
GVHD
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Alefacept
Intervention Description
IM Alefacept
Primary Outcome Measure Information:
Title
GVHD response.
Time Frame
6m
Title
Time to GVHD response
Time Frame
6m
Secondary Outcome Measure Information:
Title
Overall survival.
Time Frame
6m
Title
Disease free survival.
Time Frame
6m
Title
Occurrence of infections.
Time Frame
6m
10. Eligibility
Sex
All
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
No age limit
Resistant chronic GVHD
Exclusion Criteria:
Not fulfilling any of the inclusion criteria
Active life-threatening infection
Inability to comply with study requirements.
Known hypersensitivity to alefacept.
Active malignant disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Y Shapira, MD
Organizational Affiliation
Department of Stem cell Transplantation & Cancer immunotherapy; Cell Therapy & Transplantation Biology Research Laboratory, Hadassah University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Stem cell Transplantation & Cancer immunotherapy; Cell Therapy & Transplantation Biology Research Laboratory, Hadassah University Hospital
City
Jerusalem
ZIP/Postal Code
91120
Country
Israel
12. IPD Sharing Statement
Citations:
PubMed Identifier
16247429
Citation
Shapira MY, Resnick IB, Bitan M, Ackerstein A, Tsirigotis P, Gesundheit B, Zilberman I, Miron S, Leubovic A, Slavin S, Or R. Rapid response to alefacept given to patients with steroid resistant or steroid dependent acute graft-versus-host disease: a preliminary report. Bone Marrow Transplant. 2005 Dec;36(12):1097-101. doi: 10.1038/sj.bmt.1705185.
Results Reference
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Alefacept for Chronic Graft Versus Host Disease
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