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Alefacept for Prevention of Graft Versus Host Disease (GVHD)

Primary Purpose

Graft Versus Host Disease

Status
Terminated
Phase
Phase 3
Locations
Israel
Study Type
Interventional
Intervention
Alefacept (AMEVIVE®)
control group
Sponsored by
Hadassah Medical Organization
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Graft Versus Host Disease focused on measuring Stem cell transplantation, GVHD, Graft Versus Host Disease

Eligibility Criteria

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

Inclusion Criteria: Patient age 14-75 years old with a disease necessitating allogeneic SCT. In order to increase security, only full matched donors will be allowed and must be willing and capable of donating peripheral blood stem cells preferably, or bone marrow progenitor cells using conventional techniques, and lymphocytes if indicated. Patients must sign written informed consents. Patients must have an ECOG PS ≤ 2; creatinine < 2.0 mg/dl; ejection fraction > 40%; DLCO > 50% of predicted; serum bilirubin < 3 gm/dl; elevated GPT or GOT > 3 x normal values. Exclusion Criteria: Not fulfilling any of the inclusion criteria. Active life-threatening infection. Overt untreated infection. Hypersensitivity to alefacept. HIV seropositivity, Hepatitis B or C antigen positivity with active hepatitis. Pregnant or lactating women. Donor contraindication (HIV seropositive confirmed by western blot). Hepatitis B antigenemia. Evidence of bone marrow disease. Unable to donate bone marrow or peripheral blood due to concurrent medical condition. Inability to comply with study requirements.

Sites / Locations

  • Department of Stem Cell Transplantation & Cancer Immunotherapy

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

Alefacept

Outcomes

Primary Outcome Measures

Acute GVHD occurrence.
Acute GVHD grading.

Secondary Outcome Measures

Time to acute GVHD.
Chronic GVHD occurrence.
Chronic GVHD grading.
Engraftment/graft rejection.
Overall survival.
Disease free survival.
Infections.
Transplant-related mortality (TRM).
Immune reconstitution
Toxicity assessment according to the Common Terminology Criteria for Adverse Events (CTCAE)

Full Information

First Posted
July 31, 2006
Last Updated
April 19, 2015
Sponsor
Hadassah Medical Organization
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1. Study Identification

Unique Protocol Identification Number
NCT00361413
Brief Title
Alefacept for Prevention of Graft Versus Host Disease (GVHD)
Official Title
An Investigator Initiated Double Blind Randomized Study of Alefacept Treatment Prevention of Graft Versus Host Disease in Myeloablative Stem Cell Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
December 2010
Overall Recruitment Status
Terminated
Why Stopped
company withdrawal of the drug
Study Start Date
June 2006 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
December 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. It was shown to interfere with lymphocyte activation by specifically binding to the lymphocyte antigen, CD2, and inhibiting LFA-3/CD2 interaction. Alefacept was evaluated in two randomized, double-blind, placebo-controlled studies in adults with chronic (>1 year) plaque psoriasis and a minimum body surface area involvement of 10% who were candidates for or had previously received systemic therapy or phototherapy. 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. Graft versus host disease (GVHD) is the most ominous side effect of allogeneic 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. It was shown that CD2 depletion of allografts could prevent GVHD. Alefacept was never systemically tried in GVHD but A phase II study of BTI-322, a rat monoclonal IgG2b directed against the CD2 antigen in steroid-refractory acute GVHD showed a total response rate of 55%. We showed that alefacept might have a beneficial effect in controlling steroid resistant aGVHD and chronic GVHD. It was also shown to dramatically change the nature of transfusion associated GVHD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Graft Versus Host Disease
Keywords
Stem cell transplantation, GVHD, Graft Versus Host Disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Alefacept
Arm Title
2
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Alefacept (AMEVIVE®)
Other Intervention Name(s)
Alefacept
Intervention Description
Alefacept
Intervention Type
Drug
Intervention Name(s)
control group
Intervention Description
these patients will receive the same treatment as group A, without alefacept
Primary Outcome Measure Information:
Title
Acute GVHD occurrence.
Time Frame
100d
Title
Acute GVHD grading.
Time Frame
100d
Secondary Outcome Measure Information:
Title
Time to acute GVHD.
Time Frame
100d
Title
Chronic GVHD occurrence.
Time Frame
180d
Title
Chronic GVHD grading.
Time Frame
180d
Title
Engraftment/graft rejection.
Time Frame
21d
Title
Overall survival.
Time Frame
180d
Title
Disease free survival.
Time Frame
180d
Title
Infections.
Time Frame
180d
Title
Transplant-related mortality (TRM).
Time Frame
180d
Title
Immune reconstitution
Time Frame
180d
Title
Toxicity assessment according to the Common Terminology Criteria for Adverse Events (CTCAE)
Time Frame
180d

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient age 14-75 years old with a disease necessitating allogeneic SCT. In order to increase security, only full matched donors will be allowed and must be willing and capable of donating peripheral blood stem cells preferably, or bone marrow progenitor cells using conventional techniques, and lymphocytes if indicated. Patients must sign written informed consents. Patients must have an ECOG PS ≤ 2; creatinine < 2.0 mg/dl; ejection fraction > 40%; DLCO > 50% of predicted; serum bilirubin < 3 gm/dl; elevated GPT or GOT > 3 x normal values. Exclusion Criteria: Not fulfilling any of the inclusion criteria. Active life-threatening infection. Overt untreated infection. Hypersensitivity to alefacept. HIV seropositivity, Hepatitis B or C antigen positivity with active hepatitis. Pregnant or lactating women. Donor contraindication (HIV seropositive confirmed by western blot). Hepatitis B antigenemia. Evidence of bone marrow disease. Unable to donate bone marrow or peripheral blood due to concurrent medical condition. Inability to comply with study requirements.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Y Shapira, MD
Organizational Affiliation
Hadassah Medical Organization
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Stem Cell Transplantation & Cancer Immunotherapy
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.
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Alefacept for Prevention of Graft Versus Host Disease (GVHD)

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