<code id='E25408B40B'></code><style id='E25408B40B'></style>
    • <acronym id='E25408B40B'></acronym>
      <center id='E25408B40B'><center id='E25408B40B'><tfoot id='E25408B40B'></tfoot></center><abbr id='E25408B40B'><dir id='E25408B40B'><tfoot id='E25408B40B'></tfoot><noframes id='E25408B40B'>

    • <optgroup id='E25408B40B'><strike id='E25408B40B'><sup id='E25408B40B'></sup></strike><code id='E25408B40B'></code></optgroup>
        1. <b id='E25408B40B'><label id='E25408B40B'><select id='E25408B40B'><dt id='E25408B40B'><span id='E25408B40B'></span></dt></select></label></b><u id='E25408B40B'></u>
          <i id='E25408B40B'><strike id='E25408B40B'><tt id='E25408B40B'><pre id='E25408B40B'></pre></tt></strike></i>

          focus

          focus

          author:entertainment    Page View:69
          ASH19 CAR-T
          Victor Segura Ibarra and Rita Serda, Ph.D., NCI, NIH

          The Food and Drug Administration on Wednesday approved a futuristic new approach to treating cancer, clearing a Novartis therapy that has produced unprecedented results in patients with a rare and deadly cancer. The price tag: $475,000 for a course of treatment.

          That sounds staggering to many patients — but it’s far less than analysts expected.

          advertisement

          The therapy, called a CAR-T, is made by harvesting patients’ white blood cells and rewiring them to home in on tumors. Novartis’s product is the first CAR-T therapy to come before the FDA, leading a pack of novel treatments that promise to change the standard of care for certain aggressive blood cancers.

          Unlock this article by subscribing to STAT+ and enjoy your first 30 days free!

          GET STARTED Log In

          explore

          Walensky prepares to leave CDC — and Congress — behind
          Walensky prepares to leave CDC — and Congress — behind

          OutgoingCDCDirectorRochelleWalenskyJIMWATSON/AFPviaGettyImagesRochelleWalensky,theoutgoingdirectorof

          read more
          A disappointing year of Humira biosimilars
          A disappointing year of Humira biosimilars

          DavidJ.Phillip/APIt’sbeenoneyearsincethelaunchofthefirstadalimumabbiosimilarforHumiraintheUnitedStat

          read more
          How to save PrEP access — and even expand it
          How to save PrEP access — and even expand it

          UndertheAffordableCareAct,healthinsurersarerequiredtocoverallcostsassociatedwithpreventivecare—inclu

          read more

          There’s no way to know how good AI health technologies are

          AdobeArtificialintelligencehastheabilitytorevolutionizehumanhealth.Itisusedtodetect potentiallycance