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A Multicenter, Randomized, Double-blind, Placebo-сontrolled Comparative Study to Evaluate the Safety, Tolerability and Efficacy of XC221 Used at 100 mg Daily and at 200 mg Daily in Patients With Uncomplicated Influenza or Other Acute Viral Upper Respiratory Infections

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Trial Profile

A Multicenter, Randomized, Double-blind, Placebo-сontrolled Comparative Study to Evaluate the Safety, Tolerability and Efficacy of XC221 Used at 100 mg Daily and at 200 mg Daily in Patients With Uncomplicated Influenza or Other Acute Viral Upper Respiratory Infections

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 31 Jul 2023

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At a glance

  • Drugs XC-221 (Primary)
  • Indications Influenza virus infections; Respiratory tract infections
  • Focus Adverse reactions
  • Sponsors Valenta Pharmaceuticals
  • Most Recent Events

    • 27 May 2022 Status changed from recruiting to completed.
    • 03 Mar 2022 Planned End Date changed from 1 Feb 2022 to 1 Apr 2022.
    • 03 Mar 2022 Planned primary completion date changed from 1 Feb 2022 to 1 Apr 2022.
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