IPHARMA was authorized to conduct a Phase III clinical trial
IPHARMA was authorized by the Ministry of Healthcare of the Russian Federation to conduct a Phase III clinical trial of the drug АВ5080.
The investigational drug developer is the Chemical Diversity Research Institute.
Protocol № FLU-AV5080-03
The purpose is to assess the efficacy and safety of АВ5080 in patients with simple influenza.
The study will be conducted in 11 clinical sites. Number of patients - 875.