BRIEF-FDA Approves New Dosing Option for CRYSVITA® (burosumab-twza) in Adults With XLH

May 14 (Reuters) - Kyowa Kirin Co Ltd 4151.T:

  • FDA APPROVES NEW DOSING OPTION FOR CRYSVITA® (BUROSUMAB-TWZA) IN ADULTS WITH XLH

  • FDA APPROVES NEW DOSING OPTION FOR CRYSVITA® (BUROSUMAB-TWZA) IN ADULTS WITH XLH

  • KYOWA KIRIN - CRYSVITA DOSE MAY BE INCREASED TO 1 MG/KG EVERY 2 WEEKS AFTER 4 WEEKS

Source text: ID:nGNX1NKPXk

Further company coverage: 4151.T


This page is machine-translated. Sahm tries to improve but does not guarantee the accuracy and reliability of the translation, and will not be liable for any loss or damage caused by any inaccuracy or omission of the translation. *Disclaimer: The above content only represents the author's personal position and opinion and does not represent any position of Sahm Capital Financial Company and Sahm cannot confirm the authenticity, accuracy, and originality of the above content. Investors should consider the risks of investment products in light of their circumstances before making any investment decisions. When necessary, please consult a professional investment advisor. Sahm does not provide any investment advice, nor does it make any commitments and guarantees.