<code id='C4C21EA16F'></code><style id='C4C21EA16F'></style>
    • <acronym id='C4C21EA16F'></acronym>
      <center id='C4C21EA16F'><center id='C4C21EA16F'><tfoot id='C4C21EA16F'></tfoot></center><abbr id='C4C21EA16F'><dir id='C4C21EA16F'><tfoot id='C4C21EA16F'></tfoot><noframes id='C4C21EA16F'>

    • <optgroup id='C4C21EA16F'><strike id='C4C21EA16F'><sup id='C4C21EA16F'></sup></strike><code id='C4C21EA16F'></code></optgroup>
        1. <b id='C4C21EA16F'><label id='C4C21EA16F'><select id='C4C21EA16F'><dt id='C4C21EA16F'><span id='C4C21EA16F'></span></dt></select></label></b><u id='C4C21EA16F'></u>
          <i id='C4C21EA16F'><strike id='C4C21EA16F'><tt id='C4C21EA16F'><pre id='C4C21EA16F'></pre></tt></strike></i>

          
          WSS
          Cholesterol
          APStock

          Verve Therapeutics said Sunday that the first 10 people to receive a one-time treatment powered by a form of CRISPR called base editing showed reductions in bad cholesterol levels — study results that are preliminary but signal the potential for gene-editing treatments to benefit people with an inherited type of cardiovascular disease.

          Three of the study participants treated with potentially therapeutic doses of the Verve drug, called VERVE-101, showed  reductions in LDL-C levels of 39%, 48%, and 55%, respectively. The latter patient’s decline in so-called “bad” cholesterol was maintained for six months.

          advertisement

          The Verve-101 study results were presented at the American Heart Association conference and are the first data in patients from a therapy that uses base editing to change individual letters of DNA. Verve licensed the base-editing technology from Beam Therapeutics.

          Get unlimited access to award-winning journalism and exclusive events.

          Subscribe Log In

          Leave your comment

          Please enter your name
          Please enter your comment

          hotspot