RTF Letter a 'Hiccup'
Gilead 4Q Results, HIV Drug Outlook Encourage Analysts
By Tom Wall
Thursday, January 27, 2011
Calling it a "temporary setback," "easily remedied" and "relatively immaterial," analysts played down the negative impact of the FDA's refuse-to-file (RTF) letter to Gilead Sciences Inc. for its new drug application (NDA) seeking approval of HIV single-tablet regimen Truvada (emtricitabine/tenofovir disoproxil fumarate) plus Tibotec Pharmaceuticals Ltd.'s TMC278 (rilpivirine).
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