TARGET-NASH is a longitudinal observational cohort study of patients being managed for NASH and related conditions across the entire spectrum NAFLD in usual clinical practice. TARGET-NASH is a research registry of patients with NAFL or NASH within academic and community real-world practices maintained in order to assess the safety and effectiveness of current and future therapies.
Study Type
OBSERVATIONAL
Enrollment
7,330
Banner University Medical Center - Phoenix Transplant Center and Advanced Liver Clinic
Phoenix, Arizona, United States
Stanford University
Palo Alto, California, United States
California Liver Research Institute
Pasadena, California, United States
University of California, Davis
Sacramento, California, United States
Silicon Valley Research Institute
San Jose, California, United States
University of Colorado Anschutz Medical Campus
Aurora, Colorado, United States
Connecticut Gastroenterology
Hartford, Connecticut, United States
Connecticut Children's Medical Center
Hartford, Connecticut, United States
Medstar Georgetown Transplant Institute
Washington D.C., District of Columbia, United States
Gastro Florida
Clearwater, Florida, United States
...and 62 more locations
Establish an understanding of the current natural history of NASH at academic and community medical centers
A detailed analysis of demographics, concurrent medications, metabolic and cardiovascular co-morbidities, staging of liver disease, and outcomes for patients with NASH managed in diverse clinical settings will serve as an important comparator for subsequent interventions that alter the treatment paradigm for this disease.
Time frame: 10 years
Evaluate NASH treatment regimens being used in clinical practice
Currently, there are no FDA approved therapies for NASH, however clinicians may use a variety of interventions including diet and exercise programs, vitamin E, bariatric surgery or other unapproved uses of some cholesterol, lipid lowering, anti-diabetic and anti-inflammatory medications as well as alternative medications. TARGET-NASH will monitor the safety and effectiveness of the various treatment choices in enrolled patients.
Time frame: 10 years
Examine populations underrepresented in phase II-III clinical trials
Patients with cirrhosis, age \> 70, patients who consume moderate amounts of alcohol and patients with multiple comorbidities such as severe depression, chronic fatigue, fibromyalgia, type 2 diabetes, inflammatory bowel disease, or cardiovascular disease.
Time frame: 10 years
Evaluate optimal duration and combination of NASH therapies to achieve clinical response and clinical remission
In addition to diet and exercise, type, dose and duration of therapy of each NASH treatment (both current unapproved therapies and future FDA approved drugs) will be closely followed, with a goal to monitor treatment paradigms and various combination regimens for clinical response and clinical remission.
Time frame: 10 years
Examine liver histology
Time frame: 10 years
Estimate adverse event frequency and severity and describe management practices
NASH can often be an asymptomatic disease in the setting of other disease-related comorbidities such as diabetes and cardiovascular disease. Once NASH progresses to cirrhosis, these patients can suffer the attendant complications of decompensated liver disease including debilitating fatigue, muscle wasting, ascites, bleeding, encephalopathy, hepatocellular carcinoma, and death. NASH therapies may increase the frequency and severity of certain adverse events, such as edema (pioglitazone), some cancers (vitamin E), and new agents or combinations of agents may have their own unique adverse event profiles and varying needs for management plans (e.g., pruritus and dyslipidemia).
Time frame: 10 years
Evaluate the impact of NASH therapies on medical co-morbidities
Time frame: 10 years
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