ALZHEIMER DISEASE;
ARTICLE;
CLINICAL RESEARCH;
DIAGNOSTIC IMAGING;
DRUG COST;
DRUG MARKETING;
DRUG RESEARCH;
DRUG SAFETY;
ECONOMIC ASPECT;
HUMAN;
MOLECULAR IMAGING;
NUCLEAR MAGNETIC RESONANCE IMAGING;
POSITRON EMISSION TOMOGRAPHY;
PRIORITY JOURNAL;
SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY;
COSTS AND COST ANALYSIS;
DRUG DISCOVERY;
DRUGS, INVESTIGATIONAL;
HUMANS;
INVESTIGATIONAL NEW DRUG APPLICATION;
MARKETING;
RADIOISOTOPES;
TRANSLATIONAL MEDICAL RESEARCH;
Safety and tolerability of ultrasmall superparamagnetic iron oxide contrast agent: Comprehensive analysis of a clinical development program
Bernd H, De Kerviler E, Gaillard S, Bonnemain B. Safety and tolerability of ultrasmall superparamagnetic iron oxide contrast agent: comprehensive analysis of a clinical development program. Invest Radiol. 2009;44:336-342.
Herper M. Why Eli Lilly's Alzheimer's imaging test is no breakthrough. Forbes. http://www.forbes.com/sites/matthewherper/2012/04/09/why-eli-lillys- alzheimers- imaging-test-is-no-breakthrough/. Published April 9, 2012. Accessed January 9, 2013.
Innovation or stagnation: challenge and opportunity on the critical path to new medical products. U.S. Food and Drug Administration Web site Published March 16, 2014. Updated July 20. Accessed January 9 2012
Innovation or stagnation: challenge and opportunity on the critical path to new medical products. U.S. Food and Drug Administration Web site. http://www.fda. gov/ScienceResearch/SpecialTopics/CriticalPathInitiative/ CriticalPathOpportunitiesReports/ucm077262.htm. Published March 16, 2014. Updated July 20, 2010. Accessed January 9, 2012.
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Imaging readouts as biomarkers or surrogate parameters for the assessment of therapeutic interventions
Rudin M. Imaging readouts as biomarkers or surrogate parameters for the assessment of therapeutic interventions. Eur Radiol. 2007;17:2441-2457.