<code id='6E0723800C'></code><style id='6E0723800C'></style>
    • <acronym id='6E0723800C'></acronym>
      <center id='6E0723800C'><center id='6E0723800C'><tfoot id='6E0723800C'></tfoot></center><abbr id='6E0723800C'><dir id='6E0723800C'><tfoot id='6E0723800C'></tfoot><noframes id='6E0723800C'>

    • <optgroup id='6E0723800C'><strike id='6E0723800C'><sup id='6E0723800C'></sup></strike><code id='6E0723800C'></code></optgroup>
        1. <b id='6E0723800C'><label id='6E0723800C'><select id='6E0723800C'><dt id='6E0723800C'><span id='6E0723800C'></span></dt></select></label></b><u id='6E0723800C'></u>
          <i id='6E0723800C'><strike id='6E0723800C'><tt id='6E0723800C'><pre id='6E0723800C'></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