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This first-in-human dose-escalation study is to characterize the safety, tolerability, pharmacokinetics and pharmacodynamics of LDE225 given orally on a daily dosing schedule in patients with advanced...
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Lead Sponsor
Novartis Pharmaceuticals
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University of Pittsburgh Medical Center SC
Pittsburgh, Pennsylvania
Cancer Therapy & Research Center / UT Health Science Center InstituteForDrugDevelopment(5)
San Antonio, Texas
Novartis Investigative Site
Barcelona, Catalonia
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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