<code id='DA1974E340'></code><style id='DA1974E340'></style>
    • <acronym id='DA1974E340'></acronym>
      <center id='DA1974E340'><center id='DA1974E340'><tfoot id='DA1974E340'></tfoot></center><abbr id='DA1974E340'><dir id='DA1974E340'><tfoot id='DA1974E340'></tfoot><noframes id='DA1974E340'>

    • <optgroup id='DA1974E340'><strike id='DA1974E340'><sup id='DA1974E340'></sup></strike><code id='DA1974E340'></code></optgroup>
        1. <b id='DA1974E340'><label id='DA1974E340'><select id='DA1974E340'><dt id='DA1974E340'><span id='DA1974E340'></span></dt></select></label></b><u id='DA1974E340'></u>
          <i id='DA1974E340'><strike id='DA1974E340'><tt id='DA1974E340'><pre id='DA1974E340'></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

          entertainment