
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:title>Resmetirom and obeticholic acid for non-alcoholic steatohepatitis (NASH) : final evidence report</dc:title>
  <dc:creator>Tice, Jeffrey A., author.</dc:creator>
  <dc:creator>Fahim, Shahariar Mohammed, author.</dc:creator>
  <dc:creator>Richardson, Marina, author.</dc:creator>
  <dc:creator>Herce-Hagiwara, Belen, author.</dc:creator>
  <dc:creator>Chu, Janet N., author.</dc:creator>
  <dc:creator>Pearson, Steven D., author.</dc:creator>
  <dc:creator>Rind, David M., author.</dc:creator>
  <dc:creator>Suh, Kangho, author.</dc:creator>
  <dc:creator>Carlson, Josh, author.</dc:creator>
  <dc:creator>Dickerson, Ronald, author.</dc:creator>
  <dc:subject>Chenodeoxycholic Acid -- analogs &amp; derivatives</dc:subject>
  <dc:subject>Liver Cirrhosis -- drug therapy</dc:subject>
  <dc:subject>Non-alcoholic Fatty Liver Disease -- drug therapy</dc:subject>
  <dc:subject>Pyridazines</dc:subject>
  <dc:subject>Uracil -- analogs &amp; derivatives</dc:subject>
  <dc:description>Two oral medications are currently being evaluated as treatments for NASH with fibrosis. Resmetirom (RES) is a small molecule agonist for the thyroid hormone receptor beta (THR-beta). Obeticholic Acid (OCA) is a bile acid analog that was approved for the treatment of patients with primary biliary cholangitis (PBC) in 2016. Topline data from a phase 3 trial found that more patients treated with resmetirom 80 mg or 100 mg than placebo had ≥ 1 stage improvement in fibrosis without worsening of NASH (24% and 26% vs. 14%) and more had NASH resolution without worsening of fibrosis (26% and 30% vs. 10%). The most frequent adverse event was diarrhea (28% to 34% vs. 16% placebo); LDL-cholesterol decreased with resmetirom compared with placebo.4 More patients treated with OCA 25 mg for 18 months than placebo had achieved ≥ 1 stage improvement in fibrosis without worsening of NASH (22% vs. 10%) without significant differences between groups in NASH resolution without worsening of fibrosis.</dc:description>
  <dc:publisher>[Boston, Massachusetts] : Institute for Clinical and Economic Review, May 25, 2023</dc:publisher>
  <dc:contributor>Institute for Clinical and Economic Review, issuing body.</dc:contributor>
  <dc:contributor>Midwest Comparative Effectiveness Public Advisory Council, issuing body.</dc:contributor>
  <dc:type>Technical Report</dc:type>
  <dc:format>Text</dc:format>
  <dc:format>Illustrations</dc:format>
  <dc:format>1 online resource (1 PDF file (various pagings))</dc:format>
  <dc:identifier>nlm:nlmuid-9918697384206676-pdf</dc:identifier>
  <dc:identifier>9918697384206676</dc:identifier>
  <dc:identifier>http://resource.nlm.nih.gov/9918697384206676</dc:identifier>
  <dc:language>English</dc:language>
  <dc:coverage>United States</dc:coverage>
  <dc:rights>Reproduced with permission of the copyright holder. Further use of the material is subject to CC BY license. http://creativecommons.org/licenses/by/4.0</dc:rights>
</oai_dc:dc>
