TARGET-NASH: A 5-year longitudinal observational study of patients with nonalcoholic fatty liver disease or nonalcoholic steatohepatitis

  • sponsor
    TARGET Pharma Solutions
Updated on 23 November 2020


TARGET-NASH: A 5-year longitudinal observational study of patients with nonalcoholic fatty liver disease or nonalcoholic steatohepatitis


Data collection on patients with NAFLD/NASH to determine the natural course of the liver disease and to determine if certain lifestyle changes or diet changes that may be recommended by your doctor can affect NAFLD/NASH. Optional blood samples may be collected once a year to identify and understand the genetic reasons why certain people respond differently to certain treatments and to identify biological markers.

For more information, please view the study on,

Condition Liver Disease
Clinical Study IdentifierTX146651
SponsorTARGET Pharma Solutions
Last Modified on23 November 2020


Yes No Not Sure

Inclusion Criteria

Diagnosis of NAFLD, confirmed by imaging or histology
Diagnosis of NASH, confirmed by biopsy or confirmed by imaging with elevated liver enzymes and at least one of the following: obesity, type 2 diabetes, or dyslipidemia
No other chronic liver diseases
Cannot be participating in any other research studies for NAFLD/NASH treatment
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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