Jan 19 (Reuters) - Revive Therapeutics Ltd RVV.CD :
* REVIVE THERAPEUTICS SUBMITS UPDATED BRIEFING PACKAGE IN
SUPPORT
OF UPCOMING TYPE C MEETING GRANTED BY FDA FOR AMENDED PROTOCOL
AGREEMENT OF PHASE 3 CLINICAL STUDY FOR BUCILLAMINE IN THE
TREATMENT OF COVID-19
* REVIVE THERAPEUTICS LTD - GOAL DATE FOR FDA TO PROVIDE ITS
WRITTEN RESPONSES IS MARCH 7, 2023
* REVIVE - IF FDA AGREE WITH PROPOSED PRIMARY, SECONDARY
ENDPOINTS
OR A VERSION FDA RECOMMENDS, WILL INCORPORATE ENDPOINTS INTO
AMENDED STUDY PROTOCOL
Source text for Eikon: ID:nGNX3jvdLc
Further company coverage: RVV.CD
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