a multicentre phase IV study to collect evidence that a doravirine-based regimen can be safely and effectively administered to virologically suppressed HIV-infected patients undergoing bariatric suregery.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
8
bariatric surgery
AUC of doravirine
area under the curve, doravirine
Time frame: 24 hours
adverse events
adverse events
Time frame: 24 weeks
HIV viral load
HIV viral load
Time frame: 24 weeks
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