<code id='42BB760B26'></code><style id='42BB760B26'></style>
    • <acronym id='42BB760B26'></acronym>
      <center id='42BB760B26'><center id='42BB760B26'><tfoot id='42BB760B26'></tfoot></center><abbr id='42BB760B26'><dir id='42BB760B26'><tfoot id='42BB760B26'></tfoot><noframes id='42BB760B26'>

    • <optgroup id='42BB760B26'><strike id='42BB760B26'><sup id='42BB760B26'></sup></strike><code id='42BB760B26'></code></optgroup>
        1. <b id='42BB760B26'><label id='42BB760B26'><select id='42BB760B26'><dt id='42BB760B26'><span id='42BB760B26'></span></dt></select></label></b><u id='42BB760B26'></u>
          <i id='42BB760B26'><strike id='42BB760B26'><tt id='42BB760B26'><pre id='42BB760B26'></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