<code id='1ADDA90CAF'></code><style id='1ADDA90CAF'></style>
    • <acronym id='1ADDA90CAF'></acronym>
      <center id='1ADDA90CAF'><center id='1ADDA90CAF'><tfoot id='1ADDA90CAF'></tfoot></center><abbr id='1ADDA90CAF'><dir id='1ADDA90CAF'><tfoot id='1ADDA90CAF'></tfoot><noframes id='1ADDA90CAF'>

    • <optgroup id='1ADDA90CAF'><strike id='1ADDA90CAF'><sup id='1ADDA90CAF'></sup></strike><code id='1ADDA90CAF'></code></optgroup>
        1. <b id='1ADDA90CAF'><label id='1ADDA90CAF'><select id='1ADDA90CAF'><dt id='1ADDA90CAF'><span id='1ADDA90CAF'></span></dt></select></label></b><u id='1ADDA90CAF'></u>
          <i id='1ADDA90CAF'><strike id='1ADDA90CAF'><tt id='1ADDA90CAF'><pre id='1ADDA90CAF'></pre></tt></strike></i>

          00:00
          00:00 00:00 LIVE
          buffering
          Replay
          LIVE
          00:00 / 00:00
          LIVE
          CC
          Opacity :
          Share:
          Close

          hotspot

          author:fashion    - browse:38892
          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

          knowledge