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Study 1825: Virologically-Suppressed Adults With End Stage Renal Disease (ESRD) Receiving Chronic Hemodialysis In Study 1825, the efficacy and safety of GENVOYA once daily were evaluated in an open-label clinical trial of 55 virologically-suppressed (HIV-1 RNA less than 50 copies per mL for at least 6 months before switching to GENVOYA) HIV-1 infected subjects with ESRD (estimated creatinine clearance of less than 15 mL per minute by Cockcroft-Gault method) receiving chronic hemodialysis for at least 6 months [see Use In Specific Populations and CLINICAL PHARMACOLOGY ]
BSSCBT
Quantity:30ml | 1-month supply
C5a, complement component 5a
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US$40
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