
The randomized, single-blind, ascending dose design will assess the safety, tolerability and pharmacokinetics of single intravenous doses of OXY111A in healthy volunteers. Biomarkers in this study include the measurement of P50, which evaluates the proof of pharmacology by quantifying changes in oxygen affinity produced by OXY111A as well as cardiopulmonary exercise testing to assess clinical improvements in oxygen delivery. Following this study will be safety and efficacy studies in chronic heart failure and oncology indications... [PDF] NormOxys' Press Release -