CompletedPhase 1NCT01085201
Adenosine 2A Agonist Lexiscan in Children and Adults With Sickle Cell Disease
Studying Sickle cell disease
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Dana-Farber Cancer Institute
- Principal Investigator
- David Nathan, MD, MD, MPHDana-Farber Cancer Institute
- Intervention
- Lexiscan(drug)
- Enrollment
- 39 enrolled
- Eligibility
- 10-70 years · All sexes
- Timeline
- 2010 – 2013
Study locations (7)
- Howard University Hospital, Washington D.C., District of Columbia, United States
- Johns Hopkins University, Baltimore, Maryland, United States
- Brigham and Women's Hospital, Boston, Massachusetts, United States
- Childrens Hospital Boston, Boston, Massachusetts, United States
- Dana-Farber Cancer Institute, Boston, Massachusetts, United States
- Washington University, St Louis, Missouri, United States
- Blood Center of Wisconsin, Milwaukee, Wisconsin, United States
Collaborators
Brigham and Women's Hospital · Boston Children's Hospital · Washington University School of Medicine · Medical College of Wisconsin · Johns Hopkins University · La Jolla Institute for Allergy & Immunology · National Heart, Lung, and Blood Institute (NHLBI) · Astellas Pharma Global Development, Inc.
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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