<code id='8C22529C46'></code><style id='8C22529C46'></style>
    • <acronym id='8C22529C46'></acronym>
      <center id='8C22529C46'><center id='8C22529C46'><tfoot id='8C22529C46'></tfoot></center><abbr id='8C22529C46'><dir id='8C22529C46'><tfoot id='8C22529C46'></tfoot><noframes id='8C22529C46'>

    • <optgroup id='8C22529C46'><strike id='8C22529C46'><sup id='8C22529C46'></sup></strike><code id='8C22529C46'></code></optgroup>
        1. <b id='8C22529C46'><label id='8C22529C46'><select id='8C22529C46'><dt id='8C22529C46'><span id='8C22529C46'></span></dt></select></label></b><u id='8C22529C46'></u>
          <i id='8C22529C46'><strike id='8C22529C46'><tt id='8C22529C46'><pre id='8C22529C46'></pre></tt></strike></i>

          knowledge

          knowledge

          author:explore    Page View:339
          Alastair Grant/AP

          LONDON — AstraZeneca said Thursday it would purchase the French firm Amolyt Pharma in a deal worth up to $1 billion, picking up a rare disease drug in a pivotal trial.

          The acquisition includes an upfront payment of $800 million in cash, plus another $250 million if regulatory milestones are met. 

          advertisement

          AstraZeneca framed the deal for Amolyt, which has focused on treatments for rare endocrine diseases, as a boost for its own rare disease pipeline. 

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

          Subscribe Log In

          knowledge

          Continuity nursing helped my family in our darkest PICU moments
          Continuity nursing helped my family in our darkest PICU moments

          EssayauthorSarahMcCarthycuddleswithherdaughterMolly.CourtesySarahMcCarthyTheventilatoralarmwokemeat3

          read more
          PBMs drew scrutiny in House hearing — and so did pharma
          PBMs drew scrutiny in House hearing — and so did pharma

          Rep.JamesComer,chairoftheHouseOversightCommitteeKevinDietsch/GettyImagesWASHINGTON—Congresswantstore

          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

          People with substance use disorder deserve online privacy

          AdobeTheeraoframpant,unconsented,andunregulatedonlinedatacollectionmayfinallybewindingdownforconsume