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Milestones
1980

AMGen (Applied Molecular Genetics Inc.) established as a California corporation on April 8

George B. Rathmann named CEO

1983

Company changes name to Amgen

A research team led by Fu-Kuen Lin clones the gene for human erythropoietin (EPO) and produces recombinant EPO, later patented and named EPOGEN® (Epoetin alfa)

Initial Public Offering of 2,350,000 shares at $18 per share raises $40 million

1985

A research team led by Larry M. Souza clones the gene for human granulocyte colony-stimulating factor (G-CSF) and produces recombinant G-CSF, later patented and named NEUPOGEN®

1987

Amgen receives first patent on DNA used in producing Epoetin alfa

1988

Gordon M. Binder named CEO

1989

Immunex clones the gene for a soluble TNF receptor and later develops and patents a fusion product, Enbrel® (etanercept)

Amgen receives first U.S. patent for recombinant G-CSF (NEUPOGEN®)

FDA approves EPOGEN® for the treatment of anemia in patients with end-stage renal disease

EPOGEN® named "Product of the Year" by Fortune magazine

1991

FDA approves NEUPOGEN® to decrease the incidence of infection associated with chemotherapy-induced neutropenia in patients with non-myeloid cancers

Amgen establishes the Amgen Foundation for charitable giving

NEUPOGEN® named "Product of the Year" by Fortune magazine

Federal Appeals Court rules in Amgen’s favor in EPO patent dispute with Genetic Institute

1992

Amgen sales surpass $1 billion

1994

Amgen receives U.S. Department of Commerce National Medal of Technology

1996

Amgen sales surpass $2 billion

1998

FDA approves Enbrel® (etanercept) to treat patients with rheumatoid arthritis

1999

Amgen sales surpass $3 billion

FDA approves Enbrel® to treat moderately to severely active polyarticular-course juvenile rheumatoid arthritis

2000

Kevin W. Sharer named CEO

2001

FDA approves Aranesp® (darbepoetin alfa) to treat anemia associated with chronic renal failure

2002

FDA and EMEA approve Neulasta® (pegfilgrastim) to decrease the incidence of infection in patients with non-myeloid cancers receiving chemotherapy

FDA approves Aranesp® for the treatment of chemotherapy-induced anemia in patients with nonmyeloid malignancies
Amgen completes Immunex acquisition

FDA approves Amgen’s Rhode Island manufacturing facility for ENBREL

FDA approves Enbrel® to treat the signs and symptoms of active arthritis in patients with psoriatic arthritis

2003

FDA approves Enbrel® for the treatment of ankylosing spondylitis and other expanded indications

2004

The FDA and EMEA approve respectively Sensipar® and Mimpara® (cinacalcet HCl) for the treatment of secondary hyperparathyroidism in chronic kidney disease patients on dialysis

FDA approves Enbrel® for the treatment of chronic moderate to severe plaque psoriasis in adults
Amgen completes Tularik acquisition

FDA approves Kepivance™ (palifermin) to decrease the incidence and duration of severe oral mucositis in patients with hematologic cancers undergoing high-dose chemotherapy and bone marrow transplant.

2005

EMEA approves Kepivance® ,  Aranesp®  Sureclick™ and Neulasta®Sureclick™
Amgen Europe BV (Breda) receives Gazellen award for fastest growing company in the
province Brabant.



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