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Clinical Trials associated with Lyophilized BPI viper antivenom(University of Oxford)An Adaptive Clinical Trial to Determine the Optimal Initial Dose of Lyophilized, Species Specific Monovalent Antivenom for the Management of Systemic Envenoming by Daboia Siamensis (Eastern Russell's Viper) in Myanmar
The aim of the study is to identify an 'optimal' initial dosing of the new Burma Pharmaceutical Industry (BPI) lyophilized mono-specific antivenom for patients with systemic Daboia siamensis envenoming. The initial dosing will aim to reverse venom-induced coagulopathy (as demonstrated by a negative 20 minutes Whole Blood Clotting Time (20WBCT) at 6 hours in 95% of patients whilst causing less than 5% anaphylactic reaction.
100 Clinical Results associated with Lyophilized BPI viper antivenom(University of Oxford)
100 Translational Medicine associated with Lyophilized BPI viper antivenom(University of Oxford)
100 Patents (Medical) associated with Lyophilized BPI viper antivenom(University of Oxford)
100 Deals associated with Lyophilized BPI viper antivenom(University of Oxford)