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COMPARISON OF SAFETY &EFFICACY OF RS 79070 &ORAL PRODRUG VS IV GANCICLOVIR

$0M01FY2000RRNIH

Weill Medical College Of Cornell Univ, New York NY

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Abstract

The primary purpose of this study is to investigate the efficacy of RS-79070, a ganciclovir prodrug, as induction therapy in subjects with newly diagnosed peripheral cytomegalovirus retinitis. It will assess the safety profile of RS-79070 and the pharmacokinetics of ganciclovir following administration of RS-79070 in the target population.

View original record on NIH RePORTER →