Brief: Sorrento Reports FDA Authorization To Proceed With Phase 1 Study Of Intravenous STI-9167
April 25 (Reuters) - Sorrento Therapeutics Inc SRNE.O :
* SORRENTO ANNOUNCES FDA AUTHORIZATION TO PROCEED WITH PHASE
1
STUDY OF INTRAVENOUS STI-9167 (COVISHIELD), A POTENT
NEUTRALIZATION ANTIBODY AGAINST OMICRON BA.2 AND OTHER
SARS-COV-2 VARIANTS OF CONCERN
Source text for Eikon: ID:nGNX3XFcm7
Further company coverage: SRNE.O
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