<code id='78066DB7F2'></code><style id='78066DB7F2'></style>
    • <acronym id='78066DB7F2'></acronym>
      <center id='78066DB7F2'><center id='78066DB7F2'><tfoot id='78066DB7F2'></tfoot></center><abbr id='78066DB7F2'><dir id='78066DB7F2'><tfoot id='78066DB7F2'></tfoot><noframes id='78066DB7F2'>

    • <optgroup id='78066DB7F2'><strike id='78066DB7F2'><sup id='78066DB7F2'></sup></strike><code id='78066DB7F2'></code></optgroup>
        1. <b id='78066DB7F2'><label id='78066DB7F2'><select id='78066DB7F2'><dt id='78066DB7F2'><span id='78066DB7F2'></span></dt></select></label></b><u id='78066DB7F2'></u>
          <i id='78066DB7F2'><strike id='78066DB7F2'><tt id='78066DB7F2'><pre id='78066DB7F2'></pre></tt></strike></i>

          
          WSS
          Alnylam headquarters
          Kristoffer Tripplaar/Sipa USA/AP

          Alnylam Pharmaceuticals said Thursday that sales of its treatments for rare diseases grew 43% in the second quarter compared to the year-ago period, as the biotech prepares for a key meeting with the Food and Drug Administration in September.

          Net product sales in the quarter were $306 million, led by Amvuttra, the company’s RNAi treatment for hereditary ATTR, with sales of $132 million, exceeding Wall Street forecasts. Sales of Onpattro, its older medicine for hereditary ATTR, were $91 million, slightly less than expectations.

          advertisement

          The FDA has scheduled a meeting of outside experts on Sept. 13 to discuss the company’s application to expand the indication for Onpattro to include ATTR-CM, a related condition that affects the heart. The FDA decision is due by Oct. 8. An expansion would open a much larger market for the drug than its current approval, which largely targets nerve-related damage.

          Unlock this article by subscribing to STAT+ and enjoy your first 30 days free!

          GET STARTED Log In

          Leave your comment

          Please enter your name
          Please enter your comment

          fashion