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Gilead Sciences

EMA validates Gilead’s marketing application for Elvitegravir for treatment of HIV infection

18 June 2012 | By Gilead Sciences

Gilead Sciences announced that its MAA for elvitegravir has been validated by the EMA...

FDA Advisory Committee supports approval of Gilead’s once-daily Quad single tablet regimen for HIV

11 May 2012 | By Gilead Sciences

Final FDA decision on the Quad anticipated late summer...

FDA Advisory Committee supports approval of Gilead’s Truvada® for reducing the risk of acquiring HIV

10 May 2012 | By Gilead Sciences

Vote to support approval of once-daily oral Truvada®...

Gilead Sciences to present at the Bank of America Merrill Lynch 2012 Health Care Conference on Wednesday, May 16

8 May 2012 | By Gilead Sciences

Webcast available through Gilead Corporate website...

Gilead initiates Phase 3 clinical trial evaluating GS-1101 for the treatment of chronic lymphocytic leukemia

1 May 2012 | By Gilead Sciences

Gilead Sciences announced that the first patient has been dosed in a Phase 3 clinical trial...

Gilead Sciences to present new hepatitis B and C data at European Conference on liver disease this week

18 April 2012 | By Gilead Sciences

Presentations include first results for lead hepatitis C candidate GS-7977 in treatment-naïve genotype 1 patients...

Gilead ’s Quad single tablet regimen for HIV non-inferior to Atripla® in pivotal Phase 3 study

7 March 2012 | By Gilead Sciences Inc

Quad currently under review for marketing approval...

Gilead announces data for genotype 1 null responder hepatitis C patients enrolled in ELECTRON study

17 February 2012 | By Gilead Sciences

Viral relapse seen post treatment with GS-7977 plus ribavirin...

U.S. FDA grants Priority Review for Truvada® for reducing the risk of acquiring HIV infection

13 February 2012 | By Gilead Sciences Inc

The U.S. FDA has granted a six-month Priority Review for once-daily Truvada®...

U.S. Food and Drug Administration approves new formulations of Viread® for use by children living with HIV

18 January 2012 | By Gilead Sciences Inc

Gilead Sciences, Inc. announced that the U.S. FDA has approved Viread®...

Roy D. Baynes, MD, PhD, to join Gilead Sciences as Senior Vice President, Oncology Therapeutics

18 January 2012 | By Gilead Sciences

Gilead Sciences, Inc. announced that Roy D. Baynes, MD, PhD, will join the company...

Gilead Sciences completes acquisition of Pharmasset, Inc.

17 January 2012 | By Gilead Sciences Inc

Gilead Sciences, Inc. announced the completion to acquire Pharmasset, Inc...

Gilead Sciences completes tender offer for all outstanding shares of Pharmasset, Inc.

12 January 2012 | By Gilead Sciences

Following the merger, Pharmasset will become a wholly-owned subsidiary of Gilead...

Gilead Sciences announces early termination of Hart-Scott-Rodino waiting period

6 January 2012 | By Gilead Sciences

Gilead Sciences, Inc. has received early termination of the required waiting period...

Gilead receives European marketing authorization for Eviplera®

28 November 2011 | By Gilead Sciences Inc

Gilead Sciences, Inc. announced that the European Commission has granted marketing authorization for Eviplera®...

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