<code id='D123C0D2DE'></code><style id='D123C0D2DE'></style>
    • <acronym id='D123C0D2DE'></acronym>
      <center id='D123C0D2DE'><center id='D123C0D2DE'><tfoot id='D123C0D2DE'></tfoot></center><abbr id='D123C0D2DE'><dir id='D123C0D2DE'><tfoot id='D123C0D2DE'></tfoot><noframes id='D123C0D2DE'>

    • <optgroup id='D123C0D2DE'><strike id='D123C0D2DE'><sup id='D123C0D2DE'></sup></strike><code id='D123C0D2DE'></code></optgroup>
        1. <b id='D123C0D2DE'><label id='D123C0D2DE'><select id='D123C0D2DE'><dt id='D123C0D2DE'><span id='D123C0D2DE'></span></dt></select></label></b><u id='D123C0D2DE'></u>
          <i id='D123C0D2DE'><strike id='D123C0D2DE'><tt id='D123C0D2DE'><pre id='D123C0D2DE'></pre></tt></strike></i>

          leisure time

          leisure time

          author:hotspot    Page View:123
          Nasdaq
          Mark Lennihan/AP

          The biotech company Acelyrin, which raised more than $500 million in an IPO this year, ran into its first major setback Monday as its investigational anti-inflammatory drug missed the primary goal in a pivotal clinical trial.

          Acelyrin’s medicine, a subcutaneous treatment called izokibep, is meant to clear up lesions for patients with the common skin disease hidradenitis suppurativa, or HS, an inflammatory disorder that leads to abscesses and scars. But after 16 weeks of treatment, patients who received izokibep did not show significant improvements compared to those taking a placebo, failing the study’s primary endpoint.

          advertisement

          Acelyrin’s share price fell more than 60% in after-hours trading Monday.

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

          Subscribe Log In

          knowledge

          FDA approval of Sarepta Duchenne genetic therapy gives me hope
          FDA approval of Sarepta Duchenne genetic therapy gives me hope

          Duchennemusculardystrophyhistopathology.Dr.EdwinP.Ewing,Jr./CDCWhenIwasdiagnosedwithDuchennemuscular

          read more
          In surprise move, FDA calls for advisory committee on Lilly's Alzheimer's drug
          In surprise move, FDA calls for advisory committee on Lilly's Alzheimer's drug

          DarronCummings/APInasurprisemove,theFoodandDrugAdministrationhascalledforameetingofoutsideadvisersto

          read more
          Activists slam private health insurers over coverage restrictions
          Activists slam private health insurers over coverage restrictions

          ProtestorsoutsideAmerica'sHealthInsurancePlansheadquarters.CourtesyPeople'sActionWASHINGTON—Hun

          read more

          Gilgo Beach: Police identify another victim in serial killing investigation

          9:19KarenVergatainaphotoSuffolkCountypolicedisplayedatapressconference,Aug.4,2023,toannouncethatGilg