News & Events
Published On: 4/14/2020
TARGET-NASH Observational Study Reaches 5,000 Enrolled Patients
Now Largest Real-World Evidence Nonalcoholic Fatty Liver Disease Study in the World
TARGET PharmaSolutions, a real-world clinical data company, today announced that its nonalcoholic fatty liver disease (NAFLD) study, TARGET-NASH, reached 5,000 enrolled patients. TARGET-NASH is now the largest active observational and longitudinal NASH-specific study in the world.
“TARGET-NASH has reached 5,000 enrolled patients in only its fourth year of data collection,” said TARGET PharmaSolutions CEO, Neal Bibeau. “This regulatory-grade data is providing tremendous insight about the burden of the disease and is accelerating our partners’ understanding of these patients and the most effective strategies to bring innovative solutions to treat the disease.”
TARGET-NASH is an observational study of participants diagnosed with nonalcoholic fatty liver (NAFL) and/or NASH. The network of TARGET clinical sites includes both community and academic centers and enrolls adult and pediatric participants across the spectrum of the disease. Once enrolled, three years of retrospective data and five years of prospective data is collected from study participants, including patient-reported outcome measures and biorepository samples.
TARGET-NASH was the first disease community established by TARGET when the company launched in 2015. Since then, TARGET has developed six additional communities including hepatocellular carcinoma (HCC), inflammatory bowel disease (IBD), primary biliary cholangitis (PBC), immune-mediated inflammatory skin conditions (DERM), chronic hepatitis B (HBV), and most recently, TARGET-ASTHMA.
To create each real-world community, the TARGET model organizes groups of stakeholders around specific diseases to produce regulatory-grade data and analysis on the disease’s natural history, current treatment paradigms, and patient outcomes. Stakeholders includes key scientific leaders, regulatory agencies, pharmaceutical manufacturers, and patient advocacy groups who are involved in answering critical strategic and planning questions.
About Target RWE
Target RWE is a leading health evidence solutions company that generates innovative real-world evidence (RWE) and provides scientific intelligence tools and solutions for pharmaceutical, biotechnology, and other healthcare partners. Specifically designed to address the complexities of the natural history of disease, the drug development process and treatments in real-world settings, Target RWE builds regulatory-grade clinical data sets and applies state of the science epidemiologic methods to produce RWE about patients with specific conditions, symptoms, and therapies used in usual clinical practice.
Target RWE's regulatory-grade data sets and evidence, modern epidemiological methods, and sound scientific principles rendered as software can be utilized to better health outcomes, inform patient health guidelines, and improve overall quality of care. For more information, visit www.targetrwe.com.
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