Study identity card

Vasilyuk

Russia
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  • Study type: Randomised Clinical Trial, Treatment
  • Study type descriptors: Randomised controlled trial, Single centre
  • Objective: To investigate the bioequivalence of two formulations of Aterixen 100 mg tablets, aiming to determine if they consistently deliver the same amount of drug into the body
  • Number of participants enrolled: Enrollment data not available
  • Study enrolling from to
  • Study includes follow-up for 14 days

Study Data

  • Adults (18-64 years)
  • General population
  • Outpatient clinic
  • SARS-CoV-2
  • Pharmacological intervention
  • Antivirals
  • Aterixen

Other information

If you would like to contact the Principal Investigator of the study please email: ccb@ateneo.univr.it

The data is updated up to