A Phase II, Randomized, Placebo-Controlled Trial of Regadenoson in Sickle Cell Anemia

Status: Completed
Location: See all (12) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This research study is a Phase II clinical trial, which tests the safety and effectiveness of an investigational drug called Regadenoson (or Lexiscan) to learn whether the drug works in treating a specific disease, in this case Sickle Cell Disease (SCD). Investigational means that the drug is being studied. It also means that the FDA has not yet approved the drug for your type of disease. SCD is an inherited blood disorder that causes the red blood cells to change their shape from a round shape to a half-moon/crescent or sickled shape. People who have SCD have a different type of protein that carries oxygen in their blood (hemoglobin) than people without SCD. This different type of hemoglobin makes the red blood cells change into crescent shape under certain conditions. Sickle-shaped cells are a problem because they often get stuck in the blood vessels blocking the flow of blood, and cause inflammation and injury to important areas in the body. Regadenoson (trade name Lexiscan) is a drug that may prevent this inflammation and injury caused by the sickle shaped cells. This drug is approved by the FDA to be used as a fast infusion during a heart stress test in people who are unable to exercise enough to put stress on their heart by making the heart beat faster. Regadenoson has been studied as a long infusion at this dose in adults, and no safety issues have been identified (ClinicalTrials.gov Identifier: NCT01085201). This is the first study to look at patient benefit with the long infusion of the drug. This drug has been used in laboratory experiments and information from those other research studies suggests that this drug may help to protect the body from damage caused by sickle-shaped cells in this research study. In this research study, the investigators are specifically looking to see if Regadenoson is an effective treatment for pain crises and acute chest syndrome in SCD.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 10
Maximum Age: 70
Healthy Volunteers: f
View:

• Must have sickle cell anemia confirmed by hemoglobin analysis

• Must be admitted to hospital for pain or ACS

• Reliable IV access as determined by the study physician

• Participants must have the laboratory indices as defined below:

‣ Hemoglobin ≥ 5 g/dL

⁃ Platelets \> 100,000/mcL

⁃ ALT (SGPT) \< 3 X institutional upper limit of normal

⁃ Serum creatinine ≤ 1.5 mg/dL

⁃ INR ≤2.0, PTT ≤ 48 seconds

Locations
United States
California
Children's Hospital and Research Center at Oakland
Oakland
Illinois
University of Illinois at Chicago
Chicago
Massachusetts
Boston Children's Hospital
Boston
Brigham and Women's Hospital
Boston
Dana-Farber Cancer Institute
Boston
Maryland
Johns Hopkins University
Baltimore
Michigan
Wayne State University/Karmanos Cancer Institute
Detroit
Missouri
Washington University in St. Louis
Saint Louis
North Carolina
Duke University
Durham
Ohio
Cincinnati Children's Hospital Medical Center
Cincinnati
Texas
Baylor College of Medicine
Houston
Wisconsin
Medical College of Wisconsin
Milwaukee
Time Frame
Start Date: 2013-07
Completion Date: 2016-12-12
Participants
Target number of participants: 100
Treatments
Active_comparator: Regadenoson Arm
1.44 mcg/kg/hour infused over 48 hours
Placebo_comparator: Placebo Arm
Placebo infused over 48 hours
Sponsors
Collaborators: Washington University School of Medicine, UCSF Benioff Children's Hospital Oakland, Medical College of Wisconsin, Brigham and Women's Hospital, Children's Hospital Medical Center, Cincinnati, Duke University, Wayne State University, National Heart, Lung, and Blood Institute (NHLBI), La Jolla Institute for Allergy & Immunology, Boston Children's Hospital, Johns Hopkins University, Baylor College of Medicine, University of Illinois at Chicago
Leads: Dana-Farber Cancer Institute

This content was sourced from clinicaltrials.gov