Jan 18 (Reuters) - Celularity Inc CELU.O :
* CELULARITY RECEIVES FAST TRACK DESIGNATION FROM U.S. FDA
FOR ITS
NK CELL THERAPY CYNK-101 IN DEVELOPMENT FOR FIRST-LINE TREATMENT
OF ADVANCED HER2/NEU POSITIVE GASTRIC AND GASTROESOPHAGEAL
JUNCTION CANCERS
* CELULARITY INC - PHASE 1/2A CLINICAL TRIAL WILL EVALUATE
SAFETY
AND PRELIMINARY EFFICACY OF CYNK-101
* CELULARITY INC - SAFETY AND EFFICACY OF CYNK-101 HAVE NOT
BEEN
ESTABLISHED
* CELULARITY INC - CYNK-101 HAS NOT BEEN APPROVED FOR ANY
USE BY
U.S. FOOD AND DRUG ADMINISTRATION OR ANY OTHER ANALOGOUS
REGULATORY AUTHORITY
Source text for Eikon: ID:nGNX74lW9s
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