Dec 3 (Reuters) - Pharvaris NV PHVS.O:
PHARVARIS ANNOUNCES POSITIVE TOPLINE DATA FROM RAPIDE-3 PIVOTAL STUDY CONFIRMING POTENTIAL OF DEUCRICTIBANT FOR ON-DEMAND TREATMENT OF HAE ATTACKS
PHARVARIS NV - PRIMARY ENDPOINT MET WITH SYMPTOM RELIEF IN 1.28 HOURS
PHARVARIS NV - ALL SECONDARY EFFICACY ENDPOINTS MET IN RAPIDE-3 STUDY
PHARVARIS NV - DEUCRICTIBANT CONFIRMED TO HAVE WELL-TOLERATED SAFETY PROFILE
PHARVARIS NV - TO SUBMIT NDA TO FDA IN FIRST HALF OF 2026
Source text: ID:nGNX36XB0D
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