** Shares of drug developer TCDA.O plunges 40.2% to $4.95
premarket; second-biggest pct loser across all U.S. exchanges
** Co says FDA will need evidence of its lead experimental
drug, veverimer's effect on chronic kidney disease (CKD)
progression from a near-term interim analysis of the trial
** FDA in Aug. declined to approve veverimer, seeking
additional data regarding magnitude and durability of the drug
urn:newsml:reuters.com:*:nL4N2FQ39Z
** TCDA says it can't provide information on CKD progression
from a near-term interim analysis of the trial without
compromising the integrity of the ongoing trial
** Co also cuts workforce by more than half to 59 people to
reduce annual operating costs by ~$25 mln
** TCDA's cash and cash equivalents as of Sept. 30 were
~$375 mln urn:newsml:reuters.com:*:nBw24cQvHa
** Stock down ~78% YTD
(Reporting by Trisha Roy in Bengaluru)
((Trisha.Roy@thomsonreuters.com; within U.S. +1 646 223 8780,
outside U.S. +91 80 6182 3635;))