<code id='36E64352C6'></code><style id='36E64352C6'></style>
    • <acronym id='36E64352C6'></acronym>
      <center id='36E64352C6'><center id='36E64352C6'><tfoot id='36E64352C6'></tfoot></center><abbr id='36E64352C6'><dir id='36E64352C6'><tfoot id='36E64352C6'></tfoot><noframes id='36E64352C6'>

    • <optgroup id='36E64352C6'><strike id='36E64352C6'><sup id='36E64352C6'></sup></strike><code id='36E64352C6'></code></optgroup>
        1. <b id='36E64352C6'><label id='36E64352C6'><select id='36E64352C6'><dt id='36E64352C6'><span id='36E64352C6'></span></dt></select></label></b><u id='36E64352C6'></u>
          <i id='36E64352C6'><strike id='36E64352C6'><tt id='36E64352C6'><pre id='36E64352C6'></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