Condition: HSV Infection · Sponsor: AiCuris Anti-infective Cures AG
Randomized, open-label, multi-center, comparative trial to assess the efficacy and safety in immunocompromised subjects with acyclovir resistant or acyclovir susceptible mucocutaneous HSV infection, treated with pritelivir 100 mg once daily (following a loading dose of 400 mg as first dose to rapidly reach steady-state plasma concentration) or investigators choice, which can be either foscarnet 40 mg/kg every 8 hours or 60 mg/kg every 12 hours, or Cidofovir iv 5 mg/kg body weight given once weekly, or Cidofovir 1% or 3% topical applied 2 to 4 times daily, or Imiquimod 5% topical 3 times per week) (provided the drug is nationally approved).
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| University of Alabama at Birmingham | Birmingham, Alabama, United States | — |
| Metro Infectious Disease Consultants, LLC - Huntsville | Huntsville, Alabama, United States | — |
| University of South Alabama | Mobile, Alabama, United States | — |
| University Arizona - Department of Medicine Arizona Health Sciences Center | Tucson, Arizona, United States | — |
| City of Hope | Duarte, California, United States | — |
| Cedars-Sinai Medical Center | Los Angeles, California, United States | — |
| University of California, Division of Infectious Diseases | Sacramento, California, United States | — |
| Midland Florida Clinical Research Center, LLC | DeLand, Florida, United States | — |
| Midway Immunology and Research Center (MIRC) | Ft. Pierce, Florida, United States | — |
| University of Florida (UF) - Division of Infectious Disease | Gainesville, Florida, United States | — |
| Links Clinical Trials | Miami, Florida, United States | — |
| University of South Florida | Tampa, Florida, United States | — |
+ 58 more locations — full list on the registry record.
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