Acacia Pharma initiates phase II study with APD421 in post-operative nausea & vomitting
APD421 comprises an intravenous formulation of a currently marketed dopamine D2 antagonist for the new, patent-protected, use of management of PONV. Acacia Pharma has generated positive Phase IIa clinical data when the drug was given prophylactically to cancer patients being treated with the highly emetogenic chemotherapeutic agent, cisplatin. These data indicate that APD421 has the potential to be an effective anti-emetic in man with particular value in controlling nausea, a major unmet need.
The APD421 Phase II study is taking place in 13 major centres in France, Germany and the USA and will recruit 200 surgical patients at moderate to high risk of suffering PONV. The trial compares 3 doses of APD421 against placebo, the primary endpoint being no vomiting or retching and no requirement for anti-emetic rescue medication in the first 24 hours after surgery. The incidence and severity of nausea is being studied as a secondary endpoint. The study is expected to complete second quarter of 2012.
PONV offers Acacia Pharma a rapid, low risk development opportunity for APD421, owing to the acute nature of the condition, the large number of surgical procedures and the well-documented, benign safety profile of the active ingredient. APD421 has been widely used at much higher doses as a CNS agent for 25 years. The active ingredient in APD421 is also being developed as APD403 for the prevention of chemotherapy induced nausea & vomiting (CINV).
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