Nov 30 (Reuters) - CELYAD SA CYAD.BR :
* CELYAD DOSES FIRST MCRC PATIENT IN THE PHASE 1 ALLOSHRINK
TRIAL
EVALUATING NON-GENE EDITED ALLOGENEIC CAR-T CANDIDATE, CYAD-101
* COMPANY REGAINS FULL DEVELOPMENT AND COMMERCIALIZATION
RIGHTS TO
CYAD-101 FROM ONO PHARMACEUTICAL FOR JAPAN, KOREA AND TAIWAN
* TOPLINE DATA FROM ALLOSHRINK TRIAL ARE EXPECTED IN SECOND
HALF
OF 2019
* CELYAD CONTROLS WORLDWIDE DEVELOPMENT AND
COMMERCIALIZATION
RIGHTS TO CYAD-101
Source text for Eikon: ID:nBw7pwNv1a
Further company coverage: CYAD.BR
(Gdynia Newsroom)
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