Phase I Clinical Trial Data Review Complete - RECCE® 327 as an Intravenous Infusion Formulation
Highlights:
Independent examiners confirm Phase I R327 (I.V.) study in 80 human subjects
(eight cohorts), achieved all primary study end-points, met international regulatory
standards in data and showed R327 to be safe & well tolerated
Dosing was achieved commensurate with efficacy demonstrated in Gram-positive
& Gram-negative animal infection models to date
Phase I/II ‘fast infusion’ dosing of R327 IV is tracking to primary study end-points
with expected data read-outs in H2 2023
Phase I Clinical Trial Data Review Complete - RECCE® 327 as an...
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