Translations:Insulin analog/20/en: Difference between revisions

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Message definition (Insulin analog)
==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 [[Novo Nordisk|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]

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]