Troglitazone

Last updated
Troglitazone
Troglitazone.svg
Clinical data
Trade names Rezulin, Resulin, Romozin, Noscal
Routes of
administration 		By mouth (tablets)
ATC code
Legal status
Legal status
  • Production and promotion ceased
Pharmacokinetic data
Elimination half-life 16–34 hours
Identifiers
  • (RS)-5-(4-[(6-hydroxy-2,5,7,8-tetramethylchroman-2-yl)methoxy]benzyl)thiazolidine-2,4-dione
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
Formula C24H27NO5S
Molar mass 441.54 g·mol−1
3D model (JSmol)
Melting point 184 to 186 °C (363 to 367 °F)
  • O=C1NC(=O)SC1Cc4ccc(OCC3(Oc2c(c(c(O)c(c2CC3)C)C)C)C)cc4
  • InChI=1S/C24H27NO5S/c1-13-14(2)21-18(15(3)20(13)26)9-10-24(4,30-21)12-29-17-7-5-16(6-8-17)11-19-22(27)25-23(28)31-19/h5-8,19,26H,9-12H2,1-4H3,(H,25,27,28) Yes check.svgY
  • Key:GXPHKUHSUJUWKP-UHFFFAOYSA-N Yes check.svgY
 X mark.svgNYes check.svgY  (what is this?)    (verify)

Troglitazone is an antidiabetic and anti-inflammatory drug, and a member of the drug class of the thiazolidinediones. It was prescribed for people with diabetes mellitus type 2. [1]

Contents

It was patented in 1983 and approved for medical use in 1997. [2] It was subsequently withdrawn.

Mechanism of action

Troglitazone, like the other thiazolidinediones (pioglitazone and rosiglitazone), works by activating peroxisome proliferator-activated receptors (PPARs).

Troglitazone is a ligand to both PPARα and – more strongly – PPARγ. Troglitazone also contains an α-Tocopherol moiety, potentially giving it vitamin E-like activity in addition to its PPAR activation. It has been shown to reduce inflammation. [3] Troglitazone use was associated with a decrease of nuclear factor kappa-B (NF-κB) and a concomitant increase in its inhibitor (IκB). NFκB is an important cellular transcription regulator for the immune response.

History

A 30-tablet pharmacy stock bottle of Rezulin (troglitazone) (400 mg) from Parke-Davis. Manufactured 1997. Shown also is one broken tablet. Tablet branding is PD353. Rezulin.JPG
A 30-tablet pharmacy stock bottle of Rezulin (troglitazone) (400 mg) from Parke-Davis. Manufactured 1997. Shown also is one broken tablet. Tablet branding is PD353.

Troglitazone was developed by Daiichi Sankyo (Japan). In the United States, it was introduced and manufactured by Parke-Davis in the late 1990s but turned out to be associated with an idiosyncratic reaction leading to drug-induced hepatitis. The Food and Drug Administration (FDA) medical officer assigned to evaluate troglitazone, John Gueriguian, did not recommend its approval due to potentially high liver toxicity; Parke-Davis complained to the FDA, and Gueriguian was subsequently removed from his post. [4] A panel of experts approved it in January 1997. [5] Once the prevalence of adverse liver effects became known, troglitazone was withdrawn from the British market in December 1997, from the United States market in 2000, and from the Japanese market soon afterwards. It did not get approval in the rest of Europe.

Troglitazone was developed as the first anti-diabetic drug having a mechanism of action involving the enhancement of insulin resistance. At the time, it was widely believed that such drugs, by addressing the primary metabolic defect associated with Type 2 diabetes, would have numerous benefits including avoiding the risk of hypoglycemia associated with insulin and earlier oral antidiabetic drugs. It was further believed that reducing insulin resistance would potentially reduce the very high rate of cardiovascular disease that is associated with diabetes. [6] [7]

Parke-Davis/Warner Lambert submitted the diabetes drug Rezulin for FDA review on July 31, 1996. The medical officer assigned to the review, Dr. John L. Gueriguian, cited Rezulin's potential to harm the liver and the heart, and he questioned its viability in lowering blood sugar for patients with adult-onset diabetes, recommending against the drug's approval. After complaints from the drugmaker, Gueriguian was removed on November 4, 1996, and his review was purged by the FDA. [8] [9] Gueriguian and the company had a single meeting at which Gueriguian used "intemperate" language; the company said its objections were based on inappropriate remarks made by Gueriguian. [10] Parke-Davis said at the advisory committee that the risk of liver toxicity was comparable to placebo and that additional data of other studies confirmed this. [11] According to Peter Gøtzsche, when the company provided these additional data one week after approval, they showed a substantially greater risk for liver toxicity. [12]

The FDA approved the drug on January 29, 1997, and it appeared in pharmacies in late March. At the time, Dr. Solomon Sobel, a director at the FDA overseeing diabetes drugs, said in a New York Times interview that adverse effects of troglitazone appeared to be rare and relatively mild. [13]

Glaxo Wellcome received approval from the British Medicines Control Agency (MCA) to market troglitazone, as Romozin, in July 1997. [14] After reports of sudden liver failure in patients receiving the drug, Parke-Davis and the FDA added warnings to the drug label requiring monthly monitoring of liver enzyme levels. [15] Glaxo Wellcome removed troglitazone from the market in Britain on December 1, 1997. [8] Glaxo Wellcome had licensed the drug from Sankyo Company of Japan and had sold it in Britain from October 1, 1997. [16] [17]

On May 17, 1998, a 55-year-old patient named Audrey LaRue Jones died of acute liver failure after taking troglitazone. Importantly, she had been monitored closely by physicians at the National Institutes of Health (NIH) as a participant in the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) diabetes prevention study. [18] [19] This called into question the efficacy of the monitoring strategy. The NIH responded on June 4 by dropping troglitazone from the study. [9] [20] Dr. David J. Graham, an FDA epidemiologist charged with evaluating the drug, warned on March 26, 1999 of the dangers of using it and concluded that patient monitoring was not effective in protecting against liver failure. He estimated that the drug could be linked to over 430 liver failures and that patients incurred 1,200 times greater risk of liver failure when taking Rezulin. [9] [21] Dr. Janet B. McGill, an endocrinologist who had assisted in the Warner–Lambert's early clinical testing of Rezulin, wrote in a March 1, 2000 letter to Sen. Edward M. Kennedy (D-Mass.): "I believe that the company... deliberately omitted reports of liver toxicity and misrepresented serious adverse events experienced by patients in their clinical studies." [22]

On March 21, 2000, the FDA withdrew the drug from the market. [23] Dr. Robert I. Misbin, an FDA medical officer, wrote in a March 3, 2000 letter to Senator John Ashcroft of strong evidence that Rezulin could not be used safely. He was later threatened by the FDA with dismissal. [8] [24] By that time, the drug had been linked to 63 liver-failure deaths and had generated sales of more than $2.1 billion for Warner-Lambert. [21] The drug cost $1,400 a year per patient in 1998. [17] Pfizer, which had acquired Warner-Lambert in February 2000, reported the withdrawal of Rezulin cost $136 million. [25]

Mechanisms of hepatotoxicity

Since the withdrawal in 2000, mechanisms of troglitazone hepatotoxicity have been extensively studied using a variety of in vivo , [26] in vitro , [27] and computational methods. [28] These studies have suggested that hepatotoxicity of troglitazone results from a combination of metabolic and nonmetabolic factors. [29] The nonmetabolic toxicity is a complex function of drug-protein interactions in the liver and biliary system. Initially, the metabolic toxicity was largely associated with reactive metabolite formation from the thiazolidinedione and chromane rings of troglitazone. Moreover, the formation of quinone and o-quinone methide reactive metabolites were proposed to be formed by metabolic oxidation of the hydroxy group (OH group) of the chromane ring. [26] Detailed quantum chemical analysis of the metabolic pathways for troglitazone has shown that quinone reactive metabolite is generated by oxidation of the OH group, but o-quinone methide reactive metabolite is formed by the oxidation of the methyl groups (CH3 groups) ortho to the OH group of the chromane ring. [28] This understanding has been recently used in the design of novel troglitazone derivatives with antiproliferative activity in breast cancer cell lines. [30]

Lawsuits

In 2009, Pfizer resolved all but three of 35,000 claims over its withdrawn diabetes drug Rezulin for a total of about $750 million. Pfizer, which acquired rival Wyeth for almost $64 billion, paid about $500 million to settle Rezulin cases consolidated in federal court in New York, according to court filings. The company also paid as much as $250 million to resolve state-court suits. In 2004, it set aside $955 million to end Rezulin cases. [31]

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References

  1. ↑ Fisher L (4 November 1997). "Adverse Diabetes Drug News Sends Warner-Lambert Down". The New York Times. Retrieved 12 December 2012.
  2. ↑ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 450. ISBN   9783527607495.
  3. ↑ Aljada A, Garg R, Ghanim H, Mohanty P, Hamouda W, Assian E, Dandona P (July 2001). "Nuclear factor-kappaB suppressive and inhibitor-kappaB stimulatory effects of troglitazone in obese patients with type 2 diabetes: evidence of an antiinflammatory action?". The Journal of Clinical Endocrinology and Metabolism. 86 (7): 3250–3256. doi: 10.1210/jcem.86.7.7564 . PMID   11443197.
  4. ↑ Hintertheur A (November 2008). "Retired Drugs: Failed Blockbusters, Homicidal Tampering, Fatal Oversights". wired.com.
  5. ↑ Cohen JS (June 2006). "Risks of troglitazone apparent before approval in USA". Diabetologia. 49 (6): 1454–1455. doi: 10.1007/s00125-006-0245-0 . PMID   16601971.
  6. ↑ Henry RR (September 1996). "Effects of troglitazone on insulin sensitivity". Diabetic Medicine. 13 (9 Suppl 6): S148–S150. doi:10.1002/dme.1996.13.s6.148. PMID   8894499. S2CID   34080394.
  7. ↑ Keen H (November 1994). "Insulin resistance and the prevention of diabetes mellitus". The New England Journal of Medicine. 331 (18): 1226–1227. doi:10.1056/NEJM199411033311812. PMID   7935664.
  8. 1 2 3 Willman D (20 December 2000). "NEW FDA: Rezulin Fast-Track Approval and a Slow Withdrawal". The Los Angeles Times. Retrieved 12 December 2012.
  9. 1 2 3 Willman D (4 June 2000). "The Rise and Fall of the Killer Drug Rezulin". The Los Angeles Times. Retrieved 12 December 2012.
  10. ↑ "Report: FDA Removes Medical Officer". Associated Press .
  11. ↑ Avorn J (2005). Powerful medicines. New York: Vintage books.
  12. ↑ Gøtzsche P (2013). Deadly medicines and organised crime : how big pharma has corrupted healthcare. London [u.a.]: Radcliffe Publ. p. 185. ISBN   9781846198847.
  13. ↑ Leary W (31 January 1997). "New Class of Diabetes Drug Is Approved". The New York Times. Retrieved 12 December 2012.
  14. ↑ Sinclair N (31 July 1997). "Glaxo Wellcome gets approval for Romozin". ICIS News. Retrieved 12 December 2012.
  15. ↑ "Approval package for Rezulin (troglitazone)" (PDF). Center for Drug Evaluation and Research. U.S. Food and Drug Administration. 4 April 1997. Archived from the original (PDF) on 5 November 2014.
  16. ↑ "Diabetes drug withdrawn from sale". BBC. British Broadcasting Corporation. 1 December 1997. Retrieved 12 December 2012.
  17. 1 2 Fisher L (17 January 1998). "Drug Makers at Threshold of a New Therapy; With a Dose of Biotechnology, Big Change Is Ahead in the Treatment of Diabetes". The New York Times. Retrieved 12 December 2012.
  18. ↑ The Diabetes Prevention Program Research Group (April 1999). "The Diabetes Prevention Program. Design and methods for a clinical trial in the prevention of type 2 diabetes". Diabetes Care. 22 (4): 623–634. doi:10.2337/diacare.22.4.623. PMC   1351026 . PMID   10189543.
  19. ↑ Knowler WC, Barrett-Connor E, Fowler SE, Hamman RF, Lachin JM, Walker EA, Nathan DM (February 2002). "Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin". The New England Journal of Medicine. 346 (6): 393–403. doi:10.1056/NEJMoa012512. PMC   1370926 . PMID   11832527.
  20. ↑ Gale EA (January 2006). "Troglitazone: the lesson that nobody learned?". Diabetologia. 49 (1): 1–6. doi: 10.1007/s00125-005-0074-6 . PMID   16362281.
  21. 1 2 Willman D (16 August 2000). "FDA's Approval and Delay in Withdrawing Rezulin Probed". The Los Angeles Times. Retrieved 12 December 2012.
  22. ↑ Willman D (10 March 2000). "Fears Grow Over Delay in Removing Rezulin". The Los Angeles Times. Retrieved 12 December 2012.
  23. ↑ "2000 Safety Alerts for Human Medical Products". U.S. Food and Drug Administration. Retrieved 12 December 2012.
  24. ↑ Willman D (March 17, 2000). "Physician Who Opposes Rezulin Is Threatened by FDA With Dismissal". Los Angeles Times.
  25. ↑ "Pfizer Annual Report 2001" (PDF). Pfizer. Retrieved 12 December 2012.
  26. 1 2 Kassahun K, Pearson PG, Tang W, McIntosh I, Leung K, Elmore C, et al. (January 2001). "Studies on the metabolism of troglitazone to reactive intermediates in vitro and in vivo. Evidence for novel biotransformation pathways involving quinone methide formation and thiazolidinedione ring scission". Chemical Research in Toxicology. 14 (1): 62–70. doi:10.1021/tx000180q. PMID   11170509.
  27. ↑ Funk C, Ponelle C, Scheuermann G, Pantze M (March 2001). "Cholestatic potential of troglitazone as a possible factor contributing to troglitazone-induced hepatotoxicity: in vivo and in vitro interaction at the canalicular bile salt export pump (Bsep) in the rat". Molecular Pharmacology. 59 (3): 627–635. doi:10.1124/mol.59.3.627. PMID   11179459.
  28. 1 2 Dixit VA, Bharatam PV (July 2011). "Toxic metabolite formation from Troglitazone (TGZ): new insights from a DFT study". Chemical Research in Toxicology. 24 (7): 1113–1122. doi:10.1021/tx200110h. PMID   21657230.
  29. ↑ Masubuchi Y (October 2006). "Metabolic and non-metabolic factors determining troglitazone hepatotoxicity: a review". Drug Metabolism and Pharmacokinetics. 21 (5): 347–356. doi:10.2133/dmpk.21.347. PMID   17072088.
  30. ↑ Salamone S, Colin C, Grillier-Vuissoz I, Kuntz S, Mazerbourg S, Flament S, et al. (May 2012). "Synthesis of new troglitazone derivatives: anti-proliferative activity in breast cancer cell lines and preliminary toxicological study". European Journal of Medicinal Chemistry. 51: 206–215. doi:10.1016/j.ejmech.2012.02.044. PMID   22409968.
  31. ↑ Feeley J (March 31, 2009). "Pfizer Ends Rezulin Cases With $205 Million to Spare". Bloomberg. Retrieved 6 April 2014.
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