Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of California, San Francisco
The study involves 5 non-consecutive overnight stays and 14 additional outpatient visits at the San Francisco General Hospital Research Center.
Age
21–60
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Absence of HIV infection prior to study entry
Within 20% (+/-) of ideal body weight and must weigh at least 50kg
Healthy subjects without evidence of acute or chronic illnesses, including diabetes, high blood pressure, coronary artery disease, psychiatric illnesses, liver or kidney impairment
You may not be if
Use of illicit drugs or alcohol that could interfere with the completion of the study.
Use of any over- the- counter or prescribed drugs unless approved by the principal investigator or study physician.
Pregnant or breast- feeding.
History of acute or chronic illnesses, such as diabetes, high blood pressure, coronary artery disease, psychiatric illnesses, liver or kidney impairment.
Evidence of acute illness.
Family history of congenital prolongation of QTc interval or with any conditions known to prolong QTc interval, such as cardiac arrhythmias, bradycardia or severe heart disease
History of electrolyte abnormalities.
Clareo Health | Drug Interaction Study Between Antimalarial and Anti-HIV Medications
