** Shares of drug developer TCDA.O fall ~16% to $11.16
** Co says U.S. FDA declines to approve its lead
experimental drug, veverimer, for treatment of acid build up in
blood of patients with chronic kidney disease urn:newsml:reuters.com:*:nBw1T5blVa
** FDA is seeking additional data regarding magnitude and
durability of veverimer - TCDA
** Says there were no safety, clinical or non-clinical
issues identified in agency's letter; co plans to request a Type
A meeting with the FDA in coming weeks
** Including session's losses, stock down ~70% YTD
(Reporting by Mrinalika Roy in Bengaluru)
((mrinalika.roy@thomsonreuters.com; within U.S. +1 646 223
8780, outside U.S. +91 806749 8325;))