May 30 (Reuters) - Xeris Biopharma Holdings Inc
XERS.O :
* XERIS BIOPHARMA ANNOUNCES POSITIVE TOPLINE PHASE 2
CLINICAL DATA
OF ITS INVESTIGATIONAL XERISOL™-FORMULATED ONCE-WEEKLY
SUBCUTANEOUS (SC) LEVOTHYROXINE (XP-8121)
* XERIS BIOPHARMA HOLDINGS INC - FDA END-OF-PHASE 2
INTERACTION TO
FACILITATE A PHASE 3 PIVOTAL STUDY PROGRAM IS EXPECTED BY
YEAR-END
* XERIS BIOPHARMA HOLDINGS INC: FDA END-OF-PHASE 2
INTERACTION TO
FACILITATE A PHASE 3 PIVOTAL STUDY PROGRAM IS EXPECTED BY
YEAR-END
* XERIS BIOPHARMA- XERISOL FORMULATION ENABLED PREDICTABLE
BIOAVAILABILITY & SUSTAINED LEVELS OF LEVOTHYROXINE IN
ONCE-WEEKLY SUBCUTANEOUS PRESENTATION
Source text for Eikon: ID:nBw1MzmDqa
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