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A randomized, open label, multi-center, comparative trial, to assess the efficacy and safety of Pritelivir versus Foscarnet for the treatment of Acyclovir-resistant mucocutaneous HSV infections in immunocompromised adults

Home/A randomized, open label, multi-center, comparative trial, to assess the efficacy and safety of Pritelivir versus Foscarnet for the treatment of Acyclovir-resistant mucocutaneous HSV infections in immunocompromised adults
A randomized, open label, multi-center, comparative trial, to assess the efficacy and safety of Pritelivir versus Foscarnet for the treatment of Acyclovir-resistant mucocutaneous HSV infections in immunocompromised adultsmidwayadmin2019-04-24T18:00:35+00:00

A randomized, open label, multi-center, comparative trial, to assess the efficacy and safety of Pritelivir versus Foscarnet for the treatment of Acyclovir-resistant mucocutaneous HSV infections in immunocompromised adults

AIC316-03-II-01 · Trial ·

Major Inclusion/Exclusion Criteria

  1. Must be immunocompromised
  2. HSV lesion with clinical failure 5 days after using acyclovir, valacyclovir, or famciclovir 
  3. HSV lesion accessible for size measurement and photography 

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