<code id='C555E523B0'></code><style id='C555E523B0'></style>
    • <acronym id='C555E523B0'></acronym>
      <center id='C555E523B0'><center id='C555E523B0'><tfoot id='C555E523B0'></tfoot></center><abbr id='C555E523B0'><dir id='C555E523B0'><tfoot id='C555E523B0'></tfoot><noframes id='C555E523B0'>

    • <optgroup id='C555E523B0'><strike id='C555E523B0'><sup id='C555E523B0'></sup></strike><code id='C555E523B0'></code></optgroup>
        1. <b id='C555E523B0'><label id='C555E523B0'><select id='C555E523B0'><dt id='C555E523B0'><span id='C555E523B0'></span></dt></select></label></b><u id='C555E523B0'></u>
          <i id='C555E523B0'><strike id='C555E523B0'><tt id='C555E523B0'><pre id='C555E523B0'></pre></tt></strike></i>

          entertainment

          entertainment

          author:focus    Page View:35
          Adobe

          Acadia Pharmaceuticals said Monday that its approved medicine called Nuplazid failed to improve the social and emotional symptoms of schizophrenia in a late-stage clinical trial. 

          The negative outcome of the Phase 3 study represents a setback in the company’s efforts to expand the use of Nuplazid into the treatment of schizophrenia. The medicine is currently approved to treat hallucinations and delusions associated with Parkinson’s disease psychosis.

          advertisement

          “We are disappointed the trial did not meet its primary endpoint given the significant unmet need in patients with negative symptoms of schizophrenia,” said Acadia CEO Steve Davis, in a statement. 

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

          Subscribe Log In

          comprehensive

          Alkermes shareholders re
          Alkermes shareholders re

          MarkLennihan/APAlkermesshareholdersvotedThursdaytore-electallofthedrugmaker’scurrentdirectors,ending

          read more
          Readout Newsletter: CAR
          Readout Newsletter: CAR

          HyacinthEmpinado/STATWanttostayontopofthescienceandpoliticsdrivingbiotechtoday? Signup togetourbiote

          read more
          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

          Men with early prostate cancer can safely opt out of treatment

          AnMRIscanoftheprostate.MichaelOhliger/UCSFMendiagnosedwithearlyprostatecancercansafelychooseactivemo