Ultra-Low Dose Interleukin-2 for Refractory Chronic Graft Versus Host Disease

Completed · Phase 1

Conditions studied: Graft Versus Host Disease

In brief

The purpose of this research study is to determine the safety of IL-2 and the highest dose of this drug that can be given safely to people with chronic graft versus host disease (GVHD). Chronic GVHD is a medical condition that may occur after patients receive a bone marrow, stem cell or cord blood transplant. The donor's immune system may recognize their body (the host) as foreign and attempt to "reject" it. Traditional standard therapy to treat chronic GVHD is prednisone (steroids). Treatment options are limited, and it is thought that IL-2 may help to control chronic GVHD.

Key facts

Study ID

NCT00529035

Run by

Dana-Farber Cancer Institute

People needed

29

Starts

2007-08-01

Expected to finish

2020-05-27

Last updated by the study team

2020-07-01

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Recipients of allogeneic stem cell transplantation with myeloablative or non-myeloablative conditioning regimens
• Patients must be at least 180 days from the allogeneic stem cell transplantation procedure
• Steroid refractory cGVHD, defined as having persistent symptoms and signs of GVHD despite the use of prednisone for at least 4 weeks in the preceding 12 months without complete resolution of signs and symptoms.
• Stable dose of corticosteroids for 4 weeks prior to enrollment
• No addition or subtraction of other immunosuppressive medications for 4 weeks prior to enrollment.
• Adequate bone marrow, renal and hepatic function as outlined in the protocol
• 18 years of age or older
• ECOG Performance Status of 0-2

You may not qualify if…

• Ongoing prednisone requirement > 1mg/kg/day (or equivalent)
• Exposure to any new immunosuppressive medication in the 4 weeks prior to enrollment
• Concurrent ECP therapy within 4 weeks prior to enrollment
• Post-transplant exposure to any novel immunosuppressive medication within 100 days prior to enrollment
• Donor lymphocyte infusion within 100 days prior to IL-2 therapy
• Active malignant disease relapse
• Active, uncontrolled infection
• Positive serologic test for Hepatitis B or a positive serologic or nucleic acid test for Hepatitis C
• HIV seropositivity
• Life expectancy < 3 months
• Pregnancy or lactation
• Inability to comply with IL-2 treatment regimen
• Uncontrolled cardiac angina or symptomatic congestive heart failure
• Organ transplant (allograft) recipient

Where it is running

• Dana-Farber Cancer Institute — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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