<code id='1E22C195A6'></code><style id='1E22C195A6'></style>
    • <acronym id='1E22C195A6'></acronym>
      <center id='1E22C195A6'><center id='1E22C195A6'><tfoot id='1E22C195A6'></tfoot></center><abbr id='1E22C195A6'><dir id='1E22C195A6'><tfoot id='1E22C195A6'></tfoot><noframes id='1E22C195A6'>

    • <optgroup id='1E22C195A6'><strike id='1E22C195A6'><sup id='1E22C195A6'></sup></strike><code id='1E22C195A6'></code></optgroup>
        1. <b id='1E22C195A6'><label id='1E22C195A6'><select id='1E22C195A6'><dt id='1E22C195A6'><span id='1E22C195A6'></span></dt></select></label></b><u id='1E22C195A6'></u>
          <i id='1E22C195A6'><strike id='1E22C195A6'><tt id='1E22C195A6'><pre id='1E22C195A6'></pre></tt></strike></i>

          
          WSS
          Mark Lennihan/AP

          Pfizer on Friday said it was stopping development of a twice-daily oral obesity medication after an underwhelming clinical trial, a blow to the company’s efforts to compete in the booming field of weight-loss medications.

          The medicine, danuglipron, met its primary target in a placebo-controlled Phase 2b trial, leading to a statistically significant amount of weight lost, the company said. But the weight reductions were smaller than those seen in trials of rival medicines targeting the same GLP-1 pathway, and a high rate of patients experienced side effects and dropped out of the trial.

          advertisement

          Pfizer said it would not move twice-daily danuglipron into Phase 3 trials, but that instead it would focus on a once-daily formulation, which is currently undergoing pharmacokinetic studies. Data are expected in the first half of 2024.

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

          Subscribe Log In

          Leave your comment

          Please enter your name
          Please enter your comment

          knowledge