Sorrento Announces Phase II Results Of PD-L1 Checkpoint Inhibitor IMC-001 Presented At Asian Congress Of The European Society For Medical Oncology
December 5, 4:03 PM
IMC-001, a PD-L1 monoclonal antibody selected from Sorrento's G-MAB library, demonstrated impressive therapeutic effects in patients with heavily treated NK/T-cell lymphoma with a 60% objective response
‘Aeroclean Technologies Has Received FDA 510(K) Clearance On 11/30/2022 For Its Purgo UV Air Purifier’ – FDA
December 5, 12:04 PM
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K223328
Protalix BioTherapeutics And Chiesi Global Rare Diseases Announce U.S. FDA Acceptance Of A Resubmitted Biologics License Application For Pegunigalsidase Alfa For The Proposed Treatment Of Fabry Disease
December 5, 7:51 AM
Protalix BioTherapeutics, Inc. (NYSE:PLX) (TASE:PLX), a biopharmaceutical company focused on the development, production and commercialization of recombinant therapeutic proteins produced by its proprietary
HilleVax Announces Immunogenicity Results For Run-In Cohort Of NEST-IN1 Phase 2b Clinical Trial Of HIL-214 Norovirus Vaccine Candidate
December 5, 7:34 AM
HilleVax, Inc. (NASDAQ:HLVX), a clinical-stage biopharmaceutical company focused on developing and commercializing novel vaccines, today reported results from a prespecified immunogenicity analysis of the 203 subjects
Immuron Submits IND Application To FDA For Travelan
December 5, 7:06 AM
Investigational New Drug (IND) application submitted to the U.S. Food and Drug administration (FDA)
Plans in place to initiate a Human clinical trial in 60 healthy volunteers in the USA
Clinical Trial to examine a
Health And Human Services Issues Statement On Mpox; Says Does Not Expect That It Needs To Renew The Emergency Declaration When It Ends On January 31, 2023
December 2, 4:39 PM
https://www.hhs.gov/about/news/2022/12/02/statement-from-hhs-secretary-becerra-on-mpox.html
UroGen Announces New Data from the OPTIMA II Study; Co Says Data Show Median Durability Of Response Of 24.4 Months For UGN-102, An Investigational Non-Surgical Chemoablative Treatment For Low-Grade, Intermediate-Risk Non-Muscle Invasive Bladder Cancer
December 2, 1:01 PM
-- Results from this ongoing, noninterventional rollover study were presented at the 23rd Annual Society of Urological Oncology (SUO) Meeting in San Diego