<code id='7EFB93E49C'></code><style id='7EFB93E49C'></style>
    • <acronym id='7EFB93E49C'></acronym>
      <center id='7EFB93E49C'><center id='7EFB93E49C'><tfoot id='7EFB93E49C'></tfoot></center><abbr id='7EFB93E49C'><dir id='7EFB93E49C'><tfoot id='7EFB93E49C'></tfoot><noframes id='7EFB93E49C'>

    • <optgroup id='7EFB93E49C'><strike id='7EFB93E49C'><sup id='7EFB93E49C'></sup></strike><code id='7EFB93E49C'></code></optgroup>
        1. <b id='7EFB93E49C'><label id='7EFB93E49C'><select id='7EFB93E49C'><dt id='7EFB93E49C'><span id='7EFB93E49C'></span></dt></select></label></b><u id='7EFB93E49C'></u>
          <i id='7EFB93E49C'><strike id='7EFB93E49C'><tt id='7EFB93E49C'><pre id='7EFB93E49C'></pre></tt></strike></i>

          entertainment

          entertainment

          author:knowledge    Page View:88588
          Andrew Harnik/AP

          The Food and Drug Administration on Friday approved a new, rapid-acting medicine made by Sage Therapeutics to treat postpartum depression, the first oral treatment for the condition. But the agency denied the company’s application for an indication for major depression, a much larger potential market.

          The drug, which will be sold under the brand name Zurzuvae, is not meant to be taken chronically. Patients take it orally for 14 days. In two clinical trials, the drug was found to significantly improve depressive symptoms more than a placebo. The effect was maintained for four weeks after treatment.

          advertisement

          “Maternal mental health has been sidelined for far too long, but today’s approval of Zurzuvae helps to change that. Women have been waiting for an oral medicine that can specifically and rapidly improve the symptoms of PPD and we are proud to be able to deliver that,” said Barry Greene, Sage’s CEO, in a press release.

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

          GET STARTED Log In

          explore

          Malaria cases in Florida and Texas: Here’s what you need to know
          Malaria cases in Florida and Texas: Here’s what you need to know

          MosquitoscaughtfortestingawaitshipmenttoalabinMcAllen,Texas,inApril2016tobetestedformosquito-bornedi

          read more
          FDA approves Leqembi, a milestone in Alzheimer’s treatment
          FDA approves Leqembi, a milestone in Alzheimer’s treatment

          Amyloidplaquesformingbetweenneurons.AdobeTheFoodandDrugAdministrationonThursdaygrantedfullapprovalto

          read more
          Medicare details structure of new drug price negotiation program
          Medicare details structure of new drug price negotiation program

          MedicareonFridayreleasednewdetailsabouthowitsnewdrugpricenegotiationprogramwillwork,justtwomonthsbef

          read more

          Decaf coffee targeted by food safety group under obscure FDA rule

          ApichartWeerawong/APWASHINGTON—There’safightbrewingoverthefutureofdecafcoffee.Consumerhealthadvocate