Teriparatide

Teriparatide
Teriparatide
Clinical data
Trade names Forteo
AHFS/Drugs.com monograph
Pregnancy cat. C
Legal status  ?
Routes SubQ
Pharmacokinetic data
Bioavailability 95%
Metabolism Hepatic (nonspecific proteolysis)
Half-life SubQ: 1 hour
Excretion Renal (metabolites)
Identifiers
CAS number 52232-67-4 YesY
ATC code H05AA02
PubChem CID 16133850
DrugBank DB06285
UNII 10T9CSU89I YesY
KEGG D06078 YesY
Chemical data
Formula C181H291N55O51S2 
Mol. mass 4117.72 g/mol
 YesY(what is this?)  (verify)

Teriparatide (Forteo, also available in generic form[1]) is a recombinant form of parathyroid hormone, used in the treatment of some forms of osteoporosis.[2] It is manufactured and marketed by Eli Lilly and Company.

Contents

Administration

Teriparatide is administered by injection once a day in the thigh or abdomen. The recommended dose is 20 μg per day. Coming in the form of a penfill designed for self injection like this of insulin,2 units or 20ug is given daily, subcutaneous.

Uses

Teriparatide is indicated for use in patients with severe osteoporosis. The drug also has an ongoing clinical trial to evaluate its effectiveness in treating the symptoms of osteogenesis imperfecta.[3]

Teriparatide should not be prescribed for patients who are at increased risks for osteosarcoma. This includes those with Paget's Disease of bone or unexplained elevations of serum alkaline phosphate, open epiphysis, or prior radiation therapy involving the skeleton.

Side effects

The most commonly reported side effects are nausea, leg cramps and dizziness. The main risk of teriparatide is an increased risk of osteosarcoma, at least as seen in rat studies. Cases of bone tumor and osteosarcoma have been reported rarely in the postmarketing period.[4]

Mechanism of action

Teriparatide is the portion of human parathyroid hormone (PTH), amino acid sequence 1 through 34, of the complete molecule (containing 84 amino acids). Endogenous PTH is the primary regulator of calcium and phosphate metabolism in bone and kidney. PTH increases serum calcium, partially accomplishing this by increasing bone resorption. Thus, chronically elevated PTH will deplete bone stores. However, intermittent exposure to PTH will activate osteoblasts more than osteoclasts. Thus, once-daily injections of teriparatide have a net effect of stimulating new bone formation leading to increased bone mineral density.[5][6][7]

Teriparatide is the first, and to date only, FDA approved agent for the treatment of osteoporosis that stimulates new bone formation.[8]

FDA approval

Teriparatide was approved by the Food and Drug Administration (FDA) on 26 November 2002, for the treatment of osteoporosis in men and postmenopausal women who are at high risk for having a fracture. The drug is also approved to increase bone mass in men with primary or hypogonadal osteoporosis who are at high risk for fracture.

References

  1. ^ http://www.usvindia.com/htmls/products/injectables.html
  2. ^ Saag KG, Shane E, Boonen S, et al. (November 2007). "Teriparatide or alendronate in glucocorticoid-induced osteoporosis". The New England journal of medicine 357 (20): 2028–39. doi:10.1056/NEJMoa071408. PMID 18003959. http://content.nejm.org/cgi/pmidlookup?view=short&pmid=18003959&promo=ONFLNS19. 
  3. ^ Study of Teriparatide (FORTEO) to Treat Adults With Osteogenesis Imperfecta - Full Text View - ClinicalTrials.gov
  4. ^ http://www.drugs.com/pro/forteo.html
  5. ^ Bauer E, Aub JC, Albright F. Studies of calcium and phosphorus metabolism: V. Study of the bone trabeculae as a readily available reserve supply of calcium. J Exp Med. 1929;49:145-162.
  6. ^ Selye H. On the stimulation of new bone formation with parathyroid extract and irradiated ergosterol. Endocrinology. 1932;16:547-558.
  7. ^ Dempster, D.W., Cosman, F., Parisien, M., Shen, V., & R. Lindsay. “Anabolic actions of parathyroid hormone on bone.” (1993). Endocrine Review: 14(6): 690-709.
  8. ^ Fortéo: teriparatide (rDNA origin) injection

One randomized trial of postmenopausal women who had already fractured vertebra compared teriparatide at either 20 or 40 micrograms per day with placebo. After about 19 months, 14% of the women taking placebo had new vertebral fractures, as compared with 5% of the women taking 20 micrograms of teriparatide and 4% of the women taking 40 micrograms. There were also a statistically significant lower number of non-vertebral fractures in the teriparatide treated group. 20 micrograms of teriparatide increased spine and hip bone mineral density. no

N Engl J Med. 2001 May 10;344(19):1434-41.

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