Randomized Study: Standard of Care With or Without Atorvastatin for Prevention of GVHD for Matched Unrelated Donor BMT

Withdrawn before enrolling · Phase 3

Conditions studied: Acute Myeloid Leukemia, Acute Lymphocytic Leukemia, Myelodysplastic Syndrome

In brief

Chronic Graft Versus Host Disease (GVHD) is one of the most challenging complications in long term survivors of allogeneic stem cell transplantation. As the number of allogeneic stem cell transplantations rises annually, the incidence of chronic GVHD rates have also increased due to a variety of factors including but not limited to increasing use of peripheral blood stem cell (PBSC) grafts, increasing age of both donors and recipients, and increased use of matched unrelated donors. One study showed much lower than traditional acute GHVD rate and chronic GHVD which is similar with historical rates when atorvastatin was administered prophylactically to both the donors as well as recipients of matched related allogeneic stem cell transplantation, lead to the interest in further examining the role of Atorvastatin in relation to the development of GVHD. The investigator hypothesize that the administration of atorvastatin in recipients of matched unrelated allogeneic stem cell transplantation, a group with known higher incidence of chronic GHVD, would be a safe and effective method to reduce the incidence of chronic GVHD. Matched related allogeneic stem cell transplantation recipients will not be included in this study due to their significantly lower GVHD rates. The definition and monitoring of our primary endpoint of GVHD is well established in clinical trials in allogeneic stem cell transplantations and the investiagor will utilize the National Institutes of Health (NIH) Staging System for the diagnosis and severity assessment of chronic GVHD as well the recommendations from the NIH Consensus Conference for the conduct of clinical trials in chronic GVHD. Several secondary endpoints will be examined as defined below and include standard complementary data in the examination of clinical trials in chronic GVHD again as laid out by the NIH Consensus Conference for conduct of clinical trials in chronic GHVD.

Key facts

Study ID

NCT03066466

Run by

Loyola University

People needed

0

Starts

2019-12-10

Expected to finish

2021-02-28

Last updated by the study team

2021-04-27

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Men or women between 18-65 years of age
• Patients designated to undergo allogeneic peripheral blood or bone marrow stem cell transplantation from matched unrelated donor following the diagnosis of one of the following primary diseases in early or intermediate disease status:
• AML at the following stages at time of screening: 1st remission, 2nd remission, and 3rd or subsequent remission
• ALL at the following stages at time of screening: 1st remission, 2nd remission, and 3rd or subsequent remission
• MDS
• Patients must have Performance Score (PS) greater than 70 percent

You may not qualify if…

• Cardiac: ejection fraction less than 40 percent or other significant cardiac disease
• Pulmonary: FEV1 or DLCO less than 45 percent
• Renal: creatinine greater than the upper limit of normal
• Hepatic: bilirubin greater than 2.0 times the upper limit of normal
• CNS: documented active CNS disease
• Patients who are known to be positive for Hepatitis B surface antigen or Hepatitis C antibody, or who have tested positive for HIV

Where it is running

• Loyola University Medical Center — Maywood, Illinois, United States

Full record on ClinicalTrials.gov

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