The form that is made synthetically istetracosactide, also known assynacthen,[4]tetracosactrin andcosyntropin.[2]: 1165 [3]: 271 [5] It consists of the first 24 (of a total of 39)amino acids of ACTH and retains full function of the parent peptide.[2]: 1165 Tetracosactide stimulates the release ofcorticosteroids such ascortisol from theadrenal glands, and is used for theACTH stimulation test to assessadrenal gland function.[3]: 271
Both corticotropin and tetracosactide have been used for therapeutic purposes.[9][10] In the US the tetracosactide label is limited to diagnosis[6][7] but the UK label provides for therapeutic uses.[10]
In the US the only contraindication for tetracosactide for diagnostic use is hypersensitivity to ACTH[7] but in the UK, regulators placed contraindications for hypersensitivity to ACTH and additionally, for people with allergic disorders including asthma, acute psychosis, infectious diseases, peptic ulcer, refractory heart failure,Cushing's syndrome, treatment of primary adrenocortical insufficiency and adrenocongenital syndrome.[8]
The same contraindications that were applied in the UK for diagnostic use of tetracosactide, apply for therapeutic use of both tetracosactide and corticotropin in the US and UK.[9][10]
In addition, the US label for corticotropin for therapeutic uses includes contraindications for people who have recently had surgery, and people with scleroderma, osteoporosis, uncontrolled hypertension, or sensitivity to proteins of porcine origin; in addition the infection diseases systemic fungal infection, ocular herpes simplex, and infants who have congenital infections are specified. The label also notes that people taking corticotropin for immunosuppression should not be given live vaccines.[9]
People taking corticotropin or tetracosactide are more likely to get infections, and are at risk of hypothalamic-pituitary-axis (HPA) suppression andCushing's syndrome.[9][10]
In the normal situation, ACTH is released from thepituitary gland at the base of the brain. It acts on the adrenal glands to stimulate the production of steroid hormones (glucocorticoids). If the adrenal glands are healthy, a single injection of tetracosactide results in a rise in bloodcortisol concentrations in 30 minutes. If the adrenal glands appear not to be working then tetracosactide injection can be given to check whether the problem is due to diseased or damaged adrenals or due to lack of pituitary ACTH.
In the US, available forms of animal-derived corticotrophin have included:
Corticotrophin derived frompituitary glands from pigs, in agel formulation as well as in a zinc hydrochloride formulation, each first approved in the US in 1955 and subsequently discontinued.[11][12] In September 2015 ANI Pharmaceuticals andMerck & Co. agreed that ANI would purchase NDA 009854 and NDA 008975 and related trademarks and other assets related to these two versions of corticotrophin from Merck for $75M and ongoing royalties; the transaction closed in January 2016.[13] As of November 2016 ANI was preparing its supplemental NDA to get approval to re-introduce this formulation;[14] in 2015 ANI estimated that the US market for these products was about $1 billion per year, based on sales of Acthar gel.[13]
Corticotrophin, first approved in 1952 and subsequently discontinued; as of January 2017 this NDA was under control of Parkedale, a subsidiary ofKing Pharmaceuticals which is in turn a subsidiary ofPfizer.[15][16]
Corticotrophin branded as "Acthar", was first approved in 1950 and was subsequently discontinued; as of January 2017 this NDA was under control ofSanofi.[17]
A corticotrophin was approved in 1957 under NDA 010831, was subsequently discontinued, and as of January 2017 was under control of Organics/Lagrange, a subsidiary ofAbbvie via Abbott's acquisition ofSolvay's drug business.[18][19][20] Ageneric version under this NDA was approved under ANDA 088772 and was subsequently discontinued, and as of January 2017 was under the control ofActavis.[21]
A corticotrophin called H.P. Acthar Gel was approved in 1952 and as of January 2017 was under the control ofMallinckrodt.[22] A repository version of H.P. Acthar gel was approved in 2010 and as of January 2017 was also under the control of Mallinkrodt.[23][9]
Synthetic forms were created as a replacement for the animal-derived products.[6]
In the US, available forms of tetracosactide/cosyntropin, the synthetic form of corticotrophin, have been approved only for diagnostic uses,[6] and have included:
A branded version called Cortrosyn, which was created and developed byOrganon and was approved by the FDA in 1970, and as of January 2017 was under the control ofAmphastar Pharmaceuticals,[24][25] and there were three generic versions under ANDAs, one forMylan approved in 2009,[26] one for Sandoz/Novartis, approved in 2012,[27] and another for Amphastar under ANDA 016750.[24] This version is a powder that is reconstituted before use.[28][7]
A version of cosyntropin in solution (as opposed to powder) was developed by Sandoz/Novartis and was approved under the 505b(2) pathway in 2008; as of January 2017 it had been discontinued.[28][29][30]
In the UK, available forms of tetracosactide/cosyntropin, the synthetic form of corticotrophin, have been approved for both therapeutic and diagnostic uses, and have included:
A version branded Synacthen and provided in solution 250 mcg ampoules, for diagnostic uses, approved in 2008 and as of January 2017 controlled by Mallinckrodt.[8]
A version branded Synacthen, absorbed on to zinc phosphate, provided in milky white suspension, approved in 2008 and as of January 2017 controlled by Mallinckrodt.[10]
As of 2007, it was widely reported that tetracosactide had been used as an illegal performance-enhancing drug by professional cyclists.[31] It is known to be used as a doping agent to increase the secretion of glucocorticoids by adrenal glands.[32]
Mallinckrodt acquired the US rights to the animal-derived form via its acquisition of Questcor Pharmaceuticals in 2014.[33] When Questcor acquired the drug in 2001 it sold for $40 a vial; within a year of the acquisition Questcor raised the price of the drug to $1,500 per vial and to $28,000 by 2013.[34][35] In 2013, Questcor acquired the US rights to a competing product, Synacthen Depot, from Novartis.[35] In 2014 Mallinckrodt raised the price of Acthar further to $34,000.[36][37] TheFederal Trade Commission and attorneys general from five states sued Mallinckrodt for anti-competitive behavior with regard to the acquisition of Synacthen Depot and the monopolistic pricing of Acthar, and in January 2017 the company settled, agreeing to pay $100 million and to license Synacthen Depot to a competitor.[33] According to Kaiser Health News, Mallinckrodt responded by increasing its Congressional lobbying to $610,000, and its contributions to Congress members to $44,000, in the first quarter of 2017.[38]
In Canada, Synacthen Depot's pricing increased by 2000% in 2015, causing some provincial single payer authorities to delist the drug from funded medications. The increase in the drug's price came afterMallinckrodt acquired Questcor and its drug portfolio, which included the worldwide rights to Synacthen Depot. Prior to the price increase, Mallinckrodt claims that the drug was manufactured at a loss. Some have claimed that the price increase is abusive.[39] The drug had been priced at $33 but rose to $680 per vial. As an off-patent pharmaceutical, a similar drug, differing in formulation, available in Europe, made by a different manufacturer, sells for $8 per vial.[40]
^Kimmage P (2007). "tour 87 stage 14".Rough Ride. Yellow Jersey Press. p. 125.ISBN978-0-224-08017-0.
^Chaabo A, de Ceaurriz J, Buisson C, Tabet JC, Lasne F (February 2011). "Simultaneous quantification and qualification of synacthen in plasma".Analytical and Bioanalytical Chemistry.399 (5):1835–1843.doi:10.1007/s00216-010-4565-z.PMID21170520.S2CID28664950.
^Lathan P, Moore GE, Zambon S, Scott-Moncrieff JC (2008). "Use of a low-dose ACTH stimulation test for diagnosis of hypoadrenocorticism in dogs".Journal of Veterinary Internal Medicine.22 (4):1070–1073.doi:10.1111/j.1939-1676.2008.0118.x.PMID18537878.
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