Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Alefacept for Chronic Graft Versus Host Disease
This study is currently recruiting participants.
Verified by Hadassah Medical Organization, May 2008
Sponsored by: Hadassah Medical Organization
Information provided by: Hadassah Medical Organization
ClinicalTrials.gov Identifier: NCT00397332
  Purpose

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.


Condition Intervention Phase
Resistant Chronic GVHD
Drug: Alefacept
Phase I
Phase II

Drug Information available for: Alefacept
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Official Title: An Investigator Initiated Open-Label and Explorative Study of Alefacept Treatment for Chronic Extensive Graft Versus Host Disease

Further study details as provided by Hadassah Medical Organization:

Primary Outcome Measures:
  • GVHD response. [ Time Frame: 6m ] [ Designated as safety issue: No ]
  • Time to GVHD response [ Time Frame: 6m ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Overall survival. [ Time Frame: 6m ] [ Designated as safety issue: Yes ]
  • Disease free survival. [ Time Frame: 6m ] [ Designated as safety issue: Yes ]
  • Occurrence of infections. [ Time Frame: 6m ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 20
Study Start Date: October 2006
Estimated Study Completion Date: January 2009
Estimated Primary Completion Date: January 2009 (Final data collection date for primary outcome measure)
Intervention Details:
    Drug: Alefacept
    IM Alefacept
  Eligibility

Ages Eligible for Study:   up to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00397332

Contacts
Contact: Michael Y Shapira, MD 972-2-6778351 shapiram@hadassah.org.il

Locations
Israel
Department of Stem cell Transplantation & Cancer immunotherapy; Cell Therapy & Transplantation Biology Research Laboratory, Hadassah University Hospital Recruiting
Jerusalem, Israel, 91120
Contact: Arik Tzukert, DMD     00 972 2 6776095     arik@hadassah.org.il    
Contact: Hadas Lemberg, PhD     00 972 2 6777572     lhadas@hadassah.org.il    
Principal Investigator: Michael Y Shapira, MD            
Sponsors and Collaborators
Hadassah Medical Organization
Investigators
Principal Investigator: Michael Y Shapira, MD Department of Stem cell Transplantation & Cancer immunotherapy; Cell Therapy & Transplantation Biology Research Laboratory, Hadassah University Hospital
  More Information

Publications:
Responsible Party: Hadassah University Hospital ( Michael Shapira, MD )
Study ID Numbers: MYS-05-HMO-CTIL
Study First Received: November 8, 2006
Last Updated: May 12, 2008
ClinicalTrials.gov Identifier: NCT00397332  
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Keywords provided by Hadassah Medical Organization:
GVHD

Study placed in the following topic categories:
Alefacept
Graft versus host disease
Graft vs Host Disease
Homologous wasting disease

Additional relevant MeSH terms:
Immune System Diseases
Therapeutic Uses
Dermatologic Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 14, 2009