To determine the efficacy of oral 882C87 compared with oral acyclovir in the treatment of localized herpes zoster in immunocompromised patients. To assess the safety and tolerance of oral 882C87 in immunocompromised patients.
Patients are randomized to receive either 882C87 or acyclovir with corresponding placebos for 14 days, with two hundred patients in each of the two groups. They are stratified by presence or absence of HIV infection. Patients undergo 6 months of follow-up.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
400
Simon - Williamson Clinic
Birmingham, Alabama, United States
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
SORRA / NC Research Ctr
Birmingham, Alabama, United States
Univ of Arizona / Univ Med Ctr
Tucson, Arizona, United States
Cedars Sinai Med Ctr
Los Angeles, California, United States
AIDS Community Research Consortium
Redwood City, California, United States
Saint Francis Mem Hosp
San Francisco, California, United States
Sunnyvale Med Clinic
Sunnyvale, California, United States
Clinical Research Consultants
Trumbull, Connecticut, United States
Med Associates Clinic
Dubuque, Iowa, United States
Oschner Clinic
New Orleans, Louisiana, United States
...and 15 more locations