Nov 6 (Reuters) - Celldex Therapeutics Inc CLDX.O :
* CELLDEX THERAPEUTICS ANNOUNCES POSITIVE TOPLINE RESULTS
FROM
BARZOLVOLIMAB PHASE 2 STUDY IN CHRONIC SPONTANEOUS URTICARIA
* CELLDEX THERAPEUTICS INC: BARZOLVOLIMAB MET PRIMARY
ENDPOINT
* CELLDEX THERAPEUTICS INC: BARZOLVOLIMAB WAS GENERALLY WELL
TOLERATED WITH A FAVORABLE SAFETY PROFILE
* CELLDEX THERAPEUTICS INC: MEAN CHANGE FROM BASELINE TO
WEEK 12
IN UAS7 OF -23.87 IN 300 MG Q8W DOSE GROUP AND -23.02 IN 150 MG
Q4W DOSE GROUP
* CELLDEX THERAPEUTICS INC: TREATMENT WILL CONTINUE TO 52
WEEKS;
RESULTS SUPPORT FURTHER DEVELOPMENT OF BARZOLVOLIMAB IN PHASE 3
CSU STUDIES
* CELLDEX THERAPEUTICS INC: DATA FROM 208 PATIENTS
RANDOMIZED IN
STUDY SHOWED THAT BARZOLVOLIMAB ACHIEVED PRIMARY EFFICACY
ENDPOINT
* CELLDEX THERAPEUTICS: CLINICALLY MEANINGFUL &
STATISTICALLY
SIGNIFICANT DECREASES IN URTICARIA DISEASE ACTIVITY ACROSS
MULTIPLE DOSE GROUPS IN STUDY
Source text for Eikon: ID:nGNX19qQYq
Further company coverage: CLDX.O
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