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The U.S. Food and Drug Administration approves Yescarta™, a CD19-directed genetically modified autologous T cell immunotherapy indicated for the treatment of adult patients with relapsed or refractory large B-cell lymphoma after two or more lines of systemic therapy.
Gilead acquires Santa Monica, California-based Kite Pharma.
The U.S. Food and Drug Administration approves Vosevi™, the first pan-genotypic single tablet regimen for adults with chronic hepatitis C infection who failed certain direct-acting antiviral regimens.
The U.S. Food and Drug Administration approves Vemlidy®, a once-daily treatment for adults with chronic hepatitis B virus (HBV) infection with compensated liver disease.
The U.S. Food and Drug Administration approves Epclusa®, the first all-oral, pan-genotypic, single tablet regimen for the treatment of adults with genotype 1-6 chronic hepatitis C virus (HCV) infection.
The U.S. Food and Drug Administration approves Descovy®, a fixed-dose combination for HIV-1 infection.
The U.S. Food and Drug Administration approves Odefsey®, a complete once-daily, single tablet regimen for HIV-1 infection.
The U.S. Food and Drug Administration approves Genvoya®, a complete once-daily, single tablet regimen for HIV-1 infection.
The U.S. Food and Drug Administration approves Harvoni® for the treatment of chronic hepatitis C (CHC) genotype 1 infection in adults.
The U.S. Food and Drug Administration approves Tybost® for use in combination with other antiretroviral agents for the treatment of HIV-1 infection.
The U.S. Food and Drug Administration approves Vitekta® as part of combination antiretroviral therapy in adults with HIV-1 infection.
The U.S. Food and Drug Administration approves Zydelig® (idelalisib) for the treatment of certain patients with relapsed chronic lymphocytic leukemia (CLL) in combination with rituximab and as monotherapy for patients with relapsed follicular B-cell non-Hodgkin lymphoma (FL) and small lymphocytic lymphoma (SLL) who have received at least two prior systemic therapies.
The U.S. Food and Drug Administration approves Sovaldi® for the treatment of chronic hepatitis C (CHC) as a component of a combination antiviral treatment regimen.
Gilead acquires Mississauga, Ontario-based YM BioSciences.
The U.S. Food and Drug Administration approves Stribild®, a complete once-daily, single tablet regimen for HIV-1 infection in treatment-naïve adults.
The U.S. Food and Drug Administration approves Truvada®, in combination with safer sex practices, to reduce the risk of sexually acquired HIV-1 infection in adults at high risk.
Gilead acquires Princeton, New Jersey-based Pharmasset.
The U.S. Food and Drug Administration approves Complera®, a complete once-daily, single-tablet regimen for HIV-1 infection in treatment-naïve adults.
The U.S. Food and Drug Administration approves Cayston® for the improvement of respiratory symptoms in cystic fibrosis patients with Pseudomonas aeruginosa.
The U.S. Food and Drug Administration approves Viread® for chronic hepatitis B in adults.
Atripla® approved by Health Canada.
Gilead acquires Cork, Ireland manufacturing facility from Nycomed.
The U.S. Food and Drug Administration approves Letairis® for the treatment of pulmonary arterial hypertension.
Gilead’s Board of Directors approves a two-for-one stock split.
Gilead acquires Edmonton, Alberta-based Raylo Chemicals.
European Medicines Agency approves Truvada® for the treatment of HIV.
The U.S. Food and Drug Administration approves Macugen® for age-related macular degeneration.
The U.S. Food and Drug Administration approves Truvada®, a one-tablet, once-a-day fixed-dose co-formulation of Emtriva and Viread for HIV combination therapy.
European Medicines Agency approves Emtriva® for the treatment of HIV
The U.S. Food and Drug Administration approves Emtriva® for the treatment of HIV.
Gilead acquires Durham, North Carolina-based Triangle Pharmaceuticals.
The U.S. Food and Drug Administration approves Hepsera® for the treatment of chronic hepatitis B.
Gilead's Board of Directors approves a two-for-one stock split.
European Medicines Agency approves Viread for the treatment of HIV infection.
Gilead reports first year of positive cash flow from operations.
The U.S. Food and Drug Administration approves Viread® for the treatment of HIV infection.
The U.S. Food and Drug Administration approves AmBisome® for the treatment of cryptococcal meningitis in HIV-infected patients.
The U.S. Food and Drug Administration approves Tamiflu® for the treatment of influenza A and B in adults.
Gilead acquires Boulder, Colorado-based NeXstar Pharmaceuticals and establishes international operations.
Gilead completes its initial public offering of 5.75 million shares of Common Stock, for total proceeds of $86.25 million.
Gilead in-licenses nucleotides from The Institute of Organic Chemistry and Biochemistry at the Academy of Sciences of the Czech Republic and Rega Stichting.
AmBisome® liposome for injection receives first approval in Europe for the treatment of severe fungal infections.
Gilead Sciences is founded.