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Gilead Sciences

Gilead initiates Phase 3 clinical program for tenofovir alafenamide

24 January 2013 | By Gilead Sciences

“We are pleased to move TAF into Phase 3 clinical research...”

Gilead provides update on Hepatitis C development programs

7 January 2013 | By Gilead Sciences

Gilead Sciences announced several updates regarding its late-stage pipeline candidates for the treatment of chronic HCV infection...

Gilead Sciences to acquire YM BioSciences

12 December 2012 | By Gilead Sciences

Gilead Sciences and YM BioSciences announced that the companies have signed a definitive agreement...

Gilead Board approves two-for-one stock split

10 December 2012 | By Gilead Sciences

Gilead Sciences, Inc. announced that its Board of Directors has approved a two-for-one stock split...

European Commission approves Viread®

27 November 2012 | By Gilead Sciences, Inc.

Gilead Sciences announced that the European Commission has granted marketing authorization for two new indications for once-daily Viread®...

Gilead announces sustained virologic response rate of 78% from Phase 3 study of sofosbuvir for genotype 2/3 hepatitis C infected patients

27 November 2012 | By Gilead Sciences

Gilead Sciences announced topline results from the Phase 3 POSITRON study...

Gilead ’s Complera® non-inferior to Atripla® among treatment-naïve HIV patients

15 November 2012 | By Gilead Sciences

STaR study findings support Complera as an important single tablet regimen option...

Stribild™ maintains high viral suppression through two years of therapy among treatment-naïve HIV patients

15 November 2012 | By Gilead Sciences

Two-year results announced ...

Gilead’s once-daily novel prodrug for the treatment of HIV meets 24-week primary objective in Phase 2 study

31 October 2012 | By Gilead Sciences

Data support tenofovir alafenamide fumarate as component of future single tablet HIV regimens...

U.S. FDA approves Gilead’s Stribild™

27 August 2012 | By Gilead Sciences

Gilead Sciences, Inc. announced that the U.S. Food and Drug Administration (FDA) has approved StribildTM...

Gilead Sciences announces new collaboration with Indian partners

2 August 2012 | By Gilead Sciences, Inc.

Gilead Sciences, Inc., together with Mylan Laboratories, Ranbaxy Laboratories Limited and Strides Arcolab, have entered into agreements...

Gilead ’s Boosting Agent Cobicistat for HIV Therapy as Effective as Ritonavir in Pivotal Phase 3 Study

24 July 2012 | By Gilead Sciences, Inc.

Full clinical trial results from a pivotal Phase 3 study...

U.S. FDA approves Gilead ’s Truvada® for reducing the risk of acquiring HIV

16 July 2012 | By Gilead Sciences

The U.S. FDA has approved once-daily oral Truvada®...

Gilead submits New Drug Application to U.S. FDA for boosting agent cobicistat

28 June 2012 | By Gilead Sciences

Gilead Sciences has submitted a New Drug Application to the U.S. FDA for marketing approval of cobicistat...

Gilead submits NDA to U.S. FDA for HIV integrase inhibitor elvitegravir for treatment-experienced patients

27 June 2012 | By Gilead Sciences Inc

Elvitegravir is also a component of Quad single tablet regimen...

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