Safety and Efficacy of FTY720 in Adult Patients Who Receive a Kidney Transplant
NCT ID: NCT00099749
Last Updated: 2017-02-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2/PHASE3
255 participants
INTERVENTIONAL
2003-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Interventions
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FTY 720
Eligibility Criteria
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Inclusion Criteria
* Between 18 to 65 years old
Exclusion Criteria
18 Years
65 Years
ALL
No
Sponsors
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Novartis Pharmaceuticals
INDUSTRY
Responsible Party
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Principal Investigators
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Novartis
Role: STUDY_DIRECTOR
Novartis
Locations
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Loyola University Medical Center
Maywood, Illinois, United States
SIU School of Medicine
Springfield, Illinois, United States
St. Barnabas Medical Center
Livingston, New Jersey, United States
University of Pennsylvania
Philadelphia, Pennsylvania, United States
Rhode Island Hospital
Providence, Rhode Island, United States
Countries
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References
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Tedesco-Silva H, Szakaly P, Shoker A, Sommerer C, Yoshimura N, Schena FP, Cremer M, Hmissi A, Mayer H, Lang P; FTY720 2218 Clinical Study Group. FTY720 versus mycophenolate mofetil in de novo renal transplantation: six-month results of a double-blind study. Transplantation. 2007 Oct 15;84(7):885-92. doi: 10.1097/01.tp.0000281385.26500.3b.
Other Identifiers
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CFTY720A2218
Identifier Type: -
Identifier Source: org_study_id
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