Translations:Insulin analog/20/en
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Timeline
- 1922 Banting and Best use bovine insulin extract on human
- 1923 Eli Lilly and Company (Lilly) produces commercial quantities of bovine insulin
- 1923 Hagedorn founds the Nordisk Insulinlaboratorium in Denmark forerunner of Novo Nordisk
- 1926 Nordisk receives Danish charter to produce insulin as a non-profit
- 1936 Canadians D.M. Scott and A.M. Fisher formulate zinc insulin mixture and license to Novo
- 1936 Hagedorn discovers that adding protamine to insulin prolongs the effect of insulin
- 1946 Nordisk formulates Isophane porcine insulin a.k.a. Neutral Protamine Hagedorn or NPH insulin
- 1946 Nordisk crystallizes a protamine and insulin mixture
- 1950 Nordisk markets NPH insulin
- 1953 Novo formulates Lente porcine and bovine insulins by adding zinc for longer-lasting insulin
- 1978 Genentech develop biosynthesis of recombinant human insulin in Escherichia coli bacteria using recombinant DNA technology
- 1981 Novo Nordisk chemically and enzymatically converts porcine insulin to 'human' insulin (Actrapid HM)
- 1982 Genentech synthetic 'human' insulin approved, in partnership with Eli Lilly and Company, who shepherded the product through the U.S. Food and Drug Administration (FDA) approval process
- 1983 Lilly produces biosynthetic recombinant "rDNA insulin human INN" (Humulin)
- 1985 Axel Ullrich sequences the human insulin receptor
- 1988 Novo Nordisk produces synthetic, recombinant insulin ("insulin human INN")
- 1996 Lilly Humalog "insulin lispro INN" approved by the U.S. Food and Drug Administration
- 2003 Aventis Lantus "glargine" insulin analogue approved in USA
- 2004 Sanofi Aventis Apidra insulin "glulisine" analogue approved in the USA.
- 2006 Novo Nordisk's Levemir "insulin detemir INN" analogue approved in the USA-
- 2013 Novo Nordisk's Tresiba "insulin degludec INN" analogue approved in Europe (EMA with additional monitoring]