<code id='F936E9BC33'></code><style id='F936E9BC33'></style>
    • <acronym id='F936E9BC33'></acronym>
      <center id='F936E9BC33'><center id='F936E9BC33'><tfoot id='F936E9BC33'></tfoot></center><abbr id='F936E9BC33'><dir id='F936E9BC33'><tfoot id='F936E9BC33'></tfoot><noframes id='F936E9BC33'>

    • <optgroup id='F936E9BC33'><strike id='F936E9BC33'><sup id='F936E9BC33'></sup></strike><code id='F936E9BC33'></code></optgroup>
        1. <b id='F936E9BC33'><label id='F936E9BC33'><select id='F936E9BC33'><dt id='F936E9BC33'><span id='F936E9BC33'></span></dt></select></label></b><u id='F936E9BC33'></u>
          <i id='F936E9BC33'><strike id='F936E9BC33'><tt id='F936E9BC33'><pre id='F936E9BC33'></pre></tt></strike></i>

          
          WSS
          Peter Marks. -- health coverage from STAT
          Peter Marks, Director of the Center for Biologics Evaluation and Research at the Food and Drug Administration. Susan Walsh-Pool/Getty Images

          Peter Marks wants drug developers to ask more stupid questions.

          It’s part of the top Food and Drug Administration official’s plan to reinvigorate gene therapy, a field that has struggled despite significant technological advances. Some companies are shelving programs or going out of business, even when they have promising data. 

          advertisement

          The problems are numerous: The diseases are often exceptionally rare, limiting the potential market. Manufacturing at commercial quality is complex and expensive. Proving a drug works can be difficult, because there may be too few patients to run a traditional randomized study. 

          Get unlimited access to award-winning journalism and exclusive events.

          Subscribe Log In

          Leave your comment

          Please enter your name
          Please enter your comment

          comprehensive