Canopus gets go-ahead for Ph II trial of HCV drug
USA-based Canopus BioPharma has been granted permission by the Department of Defense to initiate a hepatitis C efficacy and safety human Phase II clinical trial, testing its patented antiviral drug CB5300.
The 15-patient, Phase II study will be conducted at Brooke Army Medical Center in Texas and will involve administering CB5300 orally to individuals with chronic hepatitis C who have not previously undergone drug treatment or therapy for the disease. The agent will be administered as a monotherapy, with detailed monitoring and reporting of viral load and liver enzymes.
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