Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Schering-Plough
Patients receive SCH 56592 oral suspension or fluconazole suspension for 14 days. Patients remain on study for 44 days total and are monitored for safety and efficacy of study treatment.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
You may be eligible for this study if you:
Are at least 18 years old.
Are HIV-positive.
Have thrush (oropharyngeal candidiasis).
Agree to practice sexual abstinence or use effective barrier methods of birth control (e.g., condoms).
Are able to take study medication and return for clinic visits during the study.
Are expected to live for at least 2 months.
You may not be if
You will not be eligible for this study if you:
Have received protease inhibitors for the first time within 30 days prior to study entry.
Have received certain medications.
Have certain other types of fungal infections.
Have certain types of cancer.
Have received SCH 56592 within 3 months prior to study entry.
Are pregnant or breast-feeding.
Cannot take medications by mouth.
Are allergic to azole drugs.
Have certain medical conditions.
Have been in this study before.
Clareo Health | Safety and Effectiveness of Fluconazole Versus SCH 56592 to Treat Thrush in HIV-Positive Patients
