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Revision as of 08:14, 7 December 2011 edit213.91.180.82 (talk) Cancer risk of DPP-4 inhibitors← Previous edit Latest revision as of 14:30, 7 January 2025 edit undo74.110.132.137 (talk) added "but not in the United States" to the end of the sentence about generic availability in order to match the drugs.com source which says it is NOT available as a generic in the US, as opposed to the Canadian and EU sources which say it is available there as a generic 
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{{Short description|Diabetes medication}}
{{Drugbox
{{Use mdy dates|date=September 2024}}
| Verifiedfields = changed
{{cs1 config |name-list-style=vanc |display-authors=6}}
| verifiedrevid = 418851502
{{Infobox drug
| IUPAC_name = (''R'')-4-oxo-4-triazolopyrazin-7(8''H'')-yl]-1-(2,4,5-trifluorophenyl)butan-2-amine
| Watchedfields = changed
| verifiedrevid = 464392221
| image = Sitagliptin.svg | image = Sitagliptin.svg
| width = 254 | width = 254
| alt =
| image2 = Sitagliptin 3D.png | image2 = Sitagliptin 3D.png
| alt2 =
| caption =


<!--Clinical data--> <!-- Clinical data -->
| pronounce = {{IPAc-en|audio=En-us-Sitagliptin.ogg|s|ɪ|t|ə|ˈ|g|l|ɪ|p|t|ɪ|n}}
| tradename =
| tradename = Januvia, Zituvio, others
| Drugs.com = {{drugs.com|monograph|januvia}}
| Drugs.com = {{drugs.com|monograph|sitagliptin}}
| MedlinePlus = a606023 | MedlinePlus = a606023
| DailyMedID = Sitagliptin
| licence_EU = Januvia
| pregnancy_AU = B3
| licence_US = Sitagliptin
| pregnancy_AU_comment =
| pregnancy_US = B
| pregnancy_category=
| routes_of_administration = ]
| class =
| ATC_prefix = A10
| ATC_suffix = BH01
| ATC_supplemental =

<!-- Legal status -->
| legal_AU = S4
| legal_AU_comment =
| legal_BR = <!-- OTC, A1, A2, A3, B1, B2, C1, C2, C3, C4, C5, D1, D2, E, F -->
| legal_BR_comment =
| legal_CA = Rx-only
| legal_CA_comment = <ref>{{cite web | title=Product monograph brand safety updates | website=Health Canada | date=February 2024 | url=https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/drug-product-database/label-safety-assessment-update/product-monograph-brand-safety-updates.html | access-date=March 24, 2024}}</ref>
| legal_DE = <!-- Anlage I, II, III or Unscheduled -->
| legal_DE_comment =
| legal_NZ = <!-- Class A, B, C -->
| legal_NZ_comment =
| legal_UK = POM | legal_UK = POM
| legal_UK_comment =
| legal_US = Rx-only | legal_US = Rx-only
| legal_US_comment = <ref name="Januvia FDA label">{{cite web | title=Januvia- sitagliptin tablet, film coated | website=DailyMed | url=https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f85a48d0-0407-4c50-b0fa-7673a160bf01 | access-date=October 15, 2021 | archive-date=October 27, 2021 | archive-url=https://web.archive.org/web/20211027142052/https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f85a48d0-0407-4c50-b0fa-7673a160bf01 | url-status=live }}</ref><ref>{{cite web | title=Zituvio- sitagliptin tablet | website=DailyMed | date=November 1, 2023 | url=https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b2da9d77-154b-48f7-8793-3f4a24dfafc6 | access-date=December 25, 2023}}</ref><ref>{{cite web | title=Zituvio- sitagliptin tablet | website=DailyMed | date=November 1, 2023 | url=https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=abfdea45-c0ca-41e3-a510-e89810bc9cfe | access-date=December 25, 2023}}</ref>
| routes_of_administration = Oral
| legal_EU = Rx-only
| legal_EU_comment = <ref name="Januvia EPAR">{{cite web | title=Januvia EPAR | website=European Medicines Agency | date=September 17, 2018 | url=https://www.ema.europa.eu/en/medicines/human/EPAR/januvia | access-date=October 15, 2021 | archive-date=October 23, 2021 | archive-url=https://web.archive.org/web/20211023091721/https://www.ema.europa.eu/en/medicines/human/EPAR/januvia | url-status=live }}</ref><ref>{{cite web | title=Xelevia EPAR | website=European Medicines Agency (EMA) | date=21 March 2007 | url=https://www.ema.europa.eu/en/medicines/human/EPAR/xelevia | access-date=19 October 2024}}</ref>
| legal_UN = <!-- N I, II, III, IV / P I, II, III, IV -->
| legal_UN_comment =
| legal_status = <!-- For countries not listed above -->


<!--Pharmacokinetic data--> <!-- Pharmacokinetic data -->
| bioavailability = 87% | bioavailability = 87%
| protein_bound = 38% | protein_bound = 38%
| metabolism = ] (]- and ]-mediated) | metabolism = ] (]- and ]-mediated)
| metabolites =
| elimination_half-life = 8 to 14 h<ref name=Herman>{{cite journal | author = Herman GA | coauthors = Stevens C, Van Dyck K, Bergman A, Yi B, De Smet M, Snyder K, Hilliard D, Tanen M, Tanaka W, Wang AQ, Zeng W, Musson D, Winchell G, Davies MJ, Ramael S, Gottesdiener KM, Wagner JA | title = Pharmacokinetics and pharmacodynamics of sitagliptin, an inhibitor of dipeptidyl peptidase IV, in healthy subjects: results from two randomized, double-blind, placebo-controlled studies with single oral doses | journal = Clin Pharmacol Ther | volume = 78 | issue = 6 | pages = 675–88 | year = 2005 | month = December | pmid = 16338283 | doi = 10.1016/j.clpt.2005.09.002}}</ref>
| onset =
| excretion = ] (80%)<ref name=Herman/>
| elimination_half-life = 8 to 14 h<ref name=Herman>{{cite journal | vauthors = Herman GA, Stevens C, van Dyck K, Bergman A, Yi B, De Smet M, Snyder K, Hilliard D, Tanen M, Tanaka W, Wang AQ, Zeng W, Musson D, Winchell G, Davies MJ, Ramael S, Gottesdiener KM, Wagner JA | display-authors = 6 | title = Pharmacokinetics and pharmacodynamics of sitagliptin, an inhibitor of dipeptidyl peptidase IV, in healthy subjects: results from two randomized, double-blind, placebo-controlled studies with single oral doses | journal = Clinical Pharmacology and Therapeutics | volume = 78 | issue = 6 | pages = 675–688 | date = December 2005 | pmid = 16338283 | doi = 10.1016/j.clpt.2005.09.002 | s2cid = 20935646 }}</ref>
| duration_of_action =
| excretion = ] (80%)<ref name=Herman/>


<!--Identifiers--> <!-- Identifiers -->
| index2_label = as salt
| CASNo_Ref = {{cascite|correct|CAS}}
| CAS_number_Ref = {{cascite|correct|??}} | CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 486460-32-6 | CAS_number = 486460-32-6
| ATC_prefix = A10 | CAS_supplemental =
| ATC_suffix = BH01
| PubChem = 4369359 | PubChem = 4369359
| IUPHAR_ligand = 6286
| DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank = DB01261 | DrugBank = DB01261
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| UNII_Ref = {{fdacite|correct|FDA}} | UNII_Ref = {{fdacite|correct|FDA}}
| UNII = QFP0P1DV7Z | UNII = QFP0P1DV7Z
| KEGG_Ref =
| ChEBI_Ref = {{ebicite|changed|EBI}}
| KEGG = D08516
| KEGG2_Ref =
| KEGG2 = D06645
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 40237 | ChEBI = 40237
| ChEMBL_Ref = {{ebicite|correct|EBI}} | ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 1422 | ChEMBL = 1422
| NIAID_ChemDB =
| PDB_ligand =
| synonyms =


<!--Chemical data--> <!-- Chemical and physical data -->
| IUPAC_name = (''R'')-4-oxo-4-triazolopyrazin-7(8''H'')-yl]-1-(2,4,5-trifluorophenyl)butan-2-amine
| C=16 | H=15 | F=6 | N=5 | O=1
| C=16 | H=15 | F=6 | N=5 | O=1
| molecular_weight = 407.314 ]/]
| smiles = Fc1cc(c(F)cc1F)C(N)CC(=O)N3Cc2nnc(n2CC3)C(F)(F)F | SMILES = Fc1cc(c(F)cc1F)C(N)CC(=O)N3Cc2nnc(n2CC3)C(F)(F)F
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C16H15F6N5O/c17-10-6-12(19)11(18)4-8(10)3-9(23)5-14(28)26-1-2-27-13(7-26)24-25-15(27)16(20,21)22/h4,6,9H,1-3,5,7,23H2/t9-/m1/s1 | StdInChI = 1S/C16H15F6N5O/c17-10-6-12(19)11(18)4-8(10)3-9(23)5-14(28)26-1-2-27-13(7-26)24-25-15(27)16(20,21)22/h4,6,9H,1-3,5,7,23H2/t9-/m1/s1
| StdInChI_comment =
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = MFFMDFFZMYYVKS-SECBINFHSA-N | StdInChIKey = MFFMDFFZMYYVKS-SECBINFHSA-N
| density =
| density_notes =
| melting_point =
| melting_high =
| melting_notes =
| boiling_point =
| boiling_notes =
| solubility =
| sol_units =
| specific_rotation =
}} }}
'''Sitagliptin''' (]; previously identified as '''MK-0431''' and marketed as sitagliptin phosphate under the trade name '''Januvia''') is an oral antihyperglycemic (]) of the ] class. It was developed, and is marketed, by ] This enzyme-inhibiting drug is used either alone or in combination with other oral antihyperglycemic agents (such as ] or a ]) for treatment of ].<ref name=medupdate01>{{cite web |title=Sitagliptin for Type 2 Diabetes |author=National Prescribing Service |date=August 2010 |accessdate=27 August, 2010 |url=http://www.nps.org.au/consumers/publications/medicine_update/issues/sitagliptin}}</ref> The benefit of this medicine is its fewer side effects (e.g., less hypoglycemia, less weight gain) in the control of blood glucose values. While safety is its advantage, efficacy is often challenged as it is often recommended to be combined with other agents like metformin. ] (Byetta) also works by its effect on the ] system.


<!-- Definition and medical uses -->
==Adverse effects==
'''Sitagliptin''', sold under the brand name '''Januvia''' among others, is an ] used to treat ].<ref name=AHFS2019/> In the United Kingdom it is listed as less preferred than ] or a ].<ref name=BNF76/> It is taken ].<ref name=AHFS2019/> It is also available in the ] medication ] (Janumet, Janumet XR).<ref name=AHFS2019/>
In ]s, ] were as common with sitagliptin (whether used alone or with ] or ]) as they were with ], except for extremely rare ] and ]-like symptoms.<ref name=RxList>{{cite web | url = http://www.rxlist.com/cgi/generic/januvia_ad.htm | title = Januvia Side Effects & Drug Interactions | year = 2007 | accessdate = 2007-11-28 | publisher = RxList.com}}</ref> There is no ] difference in the occurrence of ] between placebo and sitagliptin.<ref name=RxList/>


<!-- Side effects and mechanisms -->
There have been several ] of ] (some fatal) in people treated with sitagliptin,<ref>{{cite journal |author=Olansky L |title=Do incretin-based therapies cause acute pancreatitis? |journal=J Diabetes Sci Technol |volume=4 |issue=1 |pages=228–9 |year=2010 |pmid=20167189 |pmc=2825646}}</ref> and the U.S. package insert carries a warning to this effect,<ref>{{cite web |url=http://www.januvia.com/sitagliptin/januvia/consumer/type-2-diabetes-medicine/index.jsp?WT.svl=2?src=1&WT.srch=1&WT.mc_id=JA80G |title=Januvia for type 2 diabetes |publisher=Merck & Co. |accessdate=2010-07-31}}</ref> although the causal link between sitagliptin and pancreatitis has not yet been fully substantiated.<ref name=medupdate01 />
Common side effects include headaches, swelling of the legs, and ].<ref name=AHFS2019/> Serious side effects may include ], ], ], ], and ].<ref name=AHFS2019/> Whether use in ] or ] is safe is unclear.<ref name=Preg2019>{{cite web |title=Sitagliptin Pregnancy and Breastfeeding Warnings |url=https://www.drugs.com/pregnancy/sitagliptin.html |website=Drugs.com |access-date=March 3, 2019 |archive-date=March 6, 2019 |archive-url=https://web.archive.org/web/20190306044611/https://www.drugs.com/pregnancy/sitagliptin.html |url-status=live }}</ref> It is in the ] class and works by increasing the production of ] and decreasing the production of ] by the pancreas.<ref name=AHFS2019>{{cite web |title=Sitagliptin Monograph for Professionals |url=https://www.drugs.com/monograph/sitagliptin.html |website=Drugs.com |publisher=American Society of Health-System Pharmacists |access-date=March 3, 2019 |archive-date=March 4, 2016 |archive-url=https://web.archive.org/web/20160304075640/https://www.drugs.com/monograph/sitagliptin.html |url-status=live }}</ref>


<!-- Society and culture -->
==Cancer risk of DPP-4 inhibitors==
Sitagliptin was developed by ] and approved for medical use in the United States in 2006.<ref name=AHFS2019/> In 2022, it was the 86th most commonly prescribed medication in the United States, with more than 7{{nbsp}}million prescriptions.<ref>{{cite web | title=The Top 300 of 2022 | url=https://clincalc.com/DrugStats/Top300Drugs.aspx | website=ClinCalc | access-date=August 30, 2024 | archive-date=August 30, 2024 | archive-url=https://web.archive.org/web/20240830202410/https://clincalc.com/DrugStats/Top300Drugs.aspx | url-status=live }}</ref><ref>{{cite web | title = Sitagliptin Drug Usage Statistics, United States, 2013 - 2022 | website = ClinCalc | url = https://clincalc.com/DrugStats/Drugs/Sitagliptin | access-date = August 30, 2024 }}</ref> It is available as a ], but not in the United States.<ref>{{cite news |title=Generic Januvia Availability |url=https://www.drugs.com/availability/generic-januvia.html |access-date=December 1, 2023 |work=Drugs.com }}</ref><ref>{{cite press release | title=JAMP Pharma Group receives Health Canada approval for PrJAMP Sitagliptin, a new generic alternative for the treatment of type 2 diabetes | publisher=JAMP Pharma | via=Newswire | date=January 6, 2023 | url=https://www.newswire.ca/news-releases/jamp-pharma-group-receives-health-canada-approval-for-prjamp-sitagliptin-a-new-generic-alternative-for-the-treatment-of-type-2-diabetes-808743246.html | access-date=June 19, 2023}}</ref><ref>{{cite web | title=Sitagliptin SUN EPAR | website=European Medicines Agency (EMA) | date=December 9, 2021 | url=https://www.ema.europa.eu/en/medicines/human/EPAR/sitagliptin-sun | access-date=September 27, 2024}}</ref>
The DPP-4 enzyme is known to be involved in the suppression of certain malignancies, particularly in limiting the tissue invasion of these tumours. Inhibiting the DPP-4 enzymes may allow some cancers to progress.<ref name="pmid15375776">{{cite journal | author = Pro B, Dang NH | title = CD26/dipeptidyl peptidase IV and its role in cancer | journal = Histol. Histopathol. | volume = 19 | issue = 4 | pages = 1345–51 | year = 2004 | month = October | pmid = 15375776 | doi = | url = http://www.hh.um.es/Abstracts/Vol_19/19_4/19_4_1345.htm | issn = }}</ref><ref name="pmid15735018">{{cite journal | author = Wesley UV | coauthors = McGroarty M, Homoyouni A | title = Dipeptidyl peptidase inhibits malignant phenotype of prostate cancer cells by blocking basic fibroblast growth factor signaling pathway | journal = Cancer Res. | volume = 65 | issue = 4 | pages = 1325–34 | year = 2005 | month = February | pmid = 15735018 | doi = 10.1158/0008-5472.CAN-04-1852 }}</ref> A study of DPP-4 inhibition in human nonsmall cell lung cancer (NSCLC) concluded "DPPIV functions as a tumor suppressor, and its downregulation may contribute to the loss of growth control in NSCLC cells.<ref name="pmid15027119">{{cite journal | author = Wesley UV, Tiwari S, Houghton AN | title = Role for dipeptidyl peptidase IV in tumor suppression of human non small cell lung carcinoma cells | journal = ] | volume = 109 | issue = 6 | pages = 855–66 | year = 2004 | month = May | pmid = 15027119 | doi = 10.1002/ijc.20091 }}</ref>


==Medical uses==
The hypothetical risk of cancer activation with DPP-4 down-regulation applies to all the DPP-4 inhibitors on the market (] and ]) in addition to sitagliptin.
Sitagliptin is used to treat type 2 diabetes.<ref name=AHFS2019/> It is generally less preferred than ] or ].<ref name=BNF76>{{cite book|title=British national formulary : BNF 76|date=2018|publisher=Pharmaceutical Press|isbn=9780857113382|pages=681|edition=76}}</ref> It is taken by mouth.<ref name=AHFS2019/> It is also available as the ]s of ] (Janumet, Janumet XR)<ref name=AHFS2019/> and ] (Juvisync).<ref name=FDAJuvisyncApproval />


Sitagliptin should not be used to treat type 1 diabetes. In December 2020, the US ] (FDA) approved labeling changes stating that Januvia (sitagliptin), Janumet (sitagliptin and metformin hydrochloride), and Janumet XR (sitagliptin and metformin hydrochloride extended-release) are not proven to improve glycemic (blood sugar) control in children aged 10 to 17 with type 2 diabetes.<ref name="FDA sitagliptin 20201204" /> The drugs are approved to improve blood sugar control in adults aged 18 and older with type 2 diabetes.<ref name="FDA sitagliptin 20201204">{{cite web | title=Diabetes drug not proven to improve blood sugar in pediatric patients | website=U.S. ] (FDA) | date=December 4, 2020 | url=https://www.fda.gov/drugs/drug-safety-and-availability/new-studies-show-diabetes-drug-not-proven-improve-blood-sugar-control-pediatric-patients | access-date=December 5, 2020 | archive-date=December 4, 2020 | archive-url=https://web.archive.org/web/20201204222229/https://www.fda.gov/drugs/drug-safety-and-availability/new-studies-show-diabetes-drug-not-proven-improve-blood-sugar-control-pediatric-patients | url-status=live }} {{PD-notice}}</ref>
==History==

Sitagliptin was approved by the ] (FDA) on October 17, 2006,<ref name=FDAapproval>
==Adverse effects==
{{cite press release
Adverse effects from sitagliptin are similar to ], except for rare ], ]-like symptoms, and photosensitivity.<ref name=RxList>{{cite web | url = http://www.rxlist.com/cgi/generic/januvia_ad.htm | title = Januvia Side Effects & Drug Interactions | year = 2007 | access-date = November 28, 2007 | publisher = RxList.com | url-status = dead | archive-url = https://web.archive.org/web/20071120121831/http://www.rxlist.com/cgi/generic/januvia_ad.htm | archive-date = November 20, 2007 }}</ref> It does not increase the risk of diarrhea.<ref>{{cite journal | vauthors = Zhao Q, Hong D, Zheng D, Xiao Y, Wu B | title = Risk of diarrhea in patients with type 2 diabetes mellitus treated with sitagliptin: a meta-analysis of 30 randomized clinical trials | journal = Drug Design, Development and Therapy | volume = 8 | pages = 2283–2294 | date = 2014 | pmid = 25419118 | pmc = 4234286 | doi = 10.2147/DDDT.S70945 | doi-access = free }}</ref> No ] difference exists in the occurrence of ] between placebo and sitagliptin.<ref name=RxList/><ref>{{cite journal | vauthors = Stricklin SM, Stoecker WV, Rader RK, Hood AF, Litt JZ, Schuman TP | title = Persistent edematous-plaque photosensitivity observed with sitagliptin phosphate (Januvia®) | journal = Dermatology Online Journal | volume = 18 | issue = 2 | pages = 9 | date = February 2012 | doi = 10.5070/D30D70K7B2 | pmid = 22398230 | url = https://escholarship.org/uc/item/0d70k7b2 | access-date = June 6, 2019 | url-status = live | archive-url = https://web.archive.org/web/20190408084349/https://escholarship.org/uc/item/0d70k7b2 | archive-date = April 8, 2019 }}</ref><ref>{{cite web|url=https://www.ehealthme.com/ds/januvia/photosensitivity-reaction/|title=Januvia side effect: Photosensitivity reaction - eHealthMe|website=www.ehealthme.com|access-date=June 6, 2019|archive-date=June 7, 2019|archive-url=https://web.archive.org/web/20190607003203/https://www.ehealthme.com/ds/januvia/photosensitivity-reaction/|url-status=live}}</ref> In those taking ]s, the risk of ] is increased.<ref>{{cite journal | vauthors = Salvo F, Moore N, Arnaud M, Robinson P, Raschi E, De Ponti F, Bégaud B, Pariente A | display-authors = 6 | title = Addition of dipeptidyl peptidase-4 inhibitors to sulphonylureas and risk of hypoglycaemia: systematic review and meta-analysis | journal = BMJ | volume = 353 | pages = i2231 | date = May 2016 | pmid = 27142267 | pmc = 4854021 | doi = 10.1136/bmj.i2231 }}</ref>
| title = FDA Approves New Treatment for Diabetes

| publisher = ] (FDA)
The existence of rare case reports of ] and hypersensitivity reactions is noted in the United States prescribing information, but a causative role for sitagliptin has not been established.<ref name="Januvia FDA label" />
| date = October 17, 2006

| url = http://www.fda.gov/bbs/topics/NEWS/2006/NEW01492.html
Several ] of ] (some fatal) have been made in people treated with sitagliptin and other DPP-4 inhibitors,<ref>{{cite journal | vauthors = Olansky L | title = Do incretin-based therapies cause acute pancreatitis? | journal = Journal of Diabetes Science and Technology | volume = 4 | issue = 1 | pages = 228–229 | date = January 2010 | pmid = 20167189 | pmc = 2825646 | doi = 10.1177/193229681000400129 }}</ref><ref>{{cite web | title=FDA Drug Safety Communication: FDA investigating reports of possible increased risk of pancreatitis and pre-cancerous findings of the pancreas from incretin mimetic drugs for type 2 diabetes | website=U.S. ] (FDA) | date=June 21, 2019 | url=https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-fda-investigating-reports-possible-increased-risk-pancreatitis-and-pre | access-date=May 10, 2022 | archive-date=May 10, 2022 | archive-url=https://web.archive.org/web/20220510021433/https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-fda-investigating-reports-possible-increased-risk-pancreatitis-and-pre | url-status=live }}</ref> and the US FDA package insert carries a warning to this effect,<ref name="Januvia FDA label" /> although the causal link between sitagliptin and pancreatitis has not yet been fully substantiated.<ref name=medupdate01>{{cite web |title=Sitagliptin for Type 2 Diabetes |author=National Prescribing Service |date=August 2010 |access-date=August 27, 2010 |url=http://www.nps.org.au/consumers/publications/medicine_update/issues/sitagliptin |url-status=dead |archive-url=https://web.archive.org/web/20100718022620/http://www.nps.org.au/consumers/publications/medicine_update/issues/sitagliptin |archive-date=July 18, 2010 }}</ref> One study with lab rats published in 2009 concluded that some of the possible risks of pancreatitis or pancreatic cancer may be reduced when it is used with metformin. However, while DPP-4 inhibitors showed an increase in such risk factors, as of 2009, no increase in pancreatic cancer has been reported in individuals taking DPP-4 inhibitors.<ref>{{cite journal | vauthors = Matveyenko AV, Dry S, Cox HI, Moshtaghian A, Gurlo T, Galasso R, Butler AE, Butler PC | display-authors = 6 | title = Beneficial endocrine but adverse exocrine effects of sitagliptin in the human islet amyloid polypeptide transgenic rat model of type 2 diabetes: interactions with metformin | journal = Diabetes | volume = 58 | issue = 7 | pages = 1604–1615 | date = July 2009 | pmid = 19403868 | pmc = 2699878 | doi = 10.2337/db09-0058 }}</ref>
| accessdate = 2006-10-17 }}</ref>

and is marketed in the US as '''Januvia''' by ] On April 2, 2007, the FDA approved an oral combination of sitagliptin and ] marketed in the US as ].
In 2015, the US Food and Drug Administration (FDA) added a new warning and precaution about the risk of "severe and disabling" joint pain to the labels of all DPP-4 inhibitor medicines.<ref>{{cite web|title=DPP-4 Inhibitors for Type 2 Diabetes: Drug Safety Communication—May Cause Severe Joint Pain|url=https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-fda-warns-dpp-4-inhibitors-type-2-diabetes-may-cause-severe-joint-pain|website=U.S. ] (FDA)|access-date=September 1, 2015|date=August 28, 2015|archive-date=December 13, 2019|archive-url=https://web.archive.org/web/20191213203243/https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-fda-warns-dpp-4-inhibitors-type-2-diabetes-may-cause-severe-joint-pain|url-status=live}}</ref>


==Mechanism of action== ==Mechanism of action==
{{see also|Dipeptidyl peptidase-4 inhibitors}} {{see also|Dipeptidyl peptidase-4 inhibitors}}
Sitagliptin works to ] the ] dipeptidyl peptidase 4 (DPP-4). This enzyme breaks down the ]s ] and GIP, ]s released in response to a meal.<ref>{{cite journal | author = Herman G, Bergman A, Liu F, Stevens C, Wang A, Zeng W, Chen L, Snyder K, Hilliard D, Tanen M, Tanaka W, Meehan A, Lasseter K, Dilzer S, Blum R, Wagner J | title = Pharmacokinetics and pharmacodynamic effects of the oral DPP-4 inhibitor sitagliptin in middle-aged obese subjects. | journal = J Clin Pharmacol | volume = 46 | issue = 8 | pages = 876–86 | year = 2006 | pmid = 16855072 | doi = 10.1177/0091270006289850}}</ref> By preventing GLP-1 and GIP inactivation, they are able to increase the secretion of insulin and suppress the release of glucagon by the pancreas. This drives blood glucose levels towards normal. As the blood glucose level approaches normal, the amounts of insulin released and glucagon suppressed diminishes, thus tending to prevent an "overshoot" and subsequent low blood sugar (hypoglycemia) which is seen with some other oral hypoglycemic agents.


Sitagliptin works to ] the ] dipeptidyl peptidase 4 (DPP-4). This enzyme breaks down the ]s ] and GIP, ]s released in response to a meal.<ref>{{cite journal | vauthors = Herman GA, Bergman A, Liu F, Stevens C, Wang AQ, Zeng W, Chen L, Snyder K, Hilliard D, Tanen M, Tanaka W, Meehan AG, Lasseter K, Dilzer S, Blum R, Wagner JA | display-authors = 6 | title = Pharmacokinetics and pharmacodynamic effects of the oral DPP-4 inhibitor sitagliptin in middle-aged obese subjects | journal = Journal of Clinical Pharmacology | volume = 46 | issue = 8 | pages = 876–886 | date = August 2006 | pmid = 16855072 | doi = 10.1177/0091270006289850 | s2cid = 45849328 }}</ref> By preventing breakdown of GLP-1 and GIP, they are able to increase the secretion of insulin and suppress the release of glucagon by the alpha cells of the pancreas.{{medcn|date=May 2022}} This drives blood glucose levels towards normal.{{medcn|date=May 2022}} As the blood glucose level approaches normal, the amounts of insulin released and glucagon suppressed diminishes, thus tending to prevent an "overshoot" and subsequent low blood sugar (hypoglycemia), which is seen with some other oral hypoglycemic agents.{{medcn|date=May 2022}}
==See also==
*]
*]


Sitagliptin has been shown to lower ] level by about 0.7% points versus placebo. It is slightly less effective than metformin when used as a ]. It does not cause weight gain and has less hypoglycemia compared to sulfonylureas. Sitagliptin is recommended as a second-line drug (in combination with other drugs) after the combination of diet/exercise and metformin fails.<ref name=Gadsby2009>{{cite journal| vauthors = Gadsby R |title=Efficacy and Safety of Sitagliptin in the Treatment of Type 2 Diabetes|journal=Clinical Medicine: Therapeutics |year=2009 |volume=1 |issue=1 |pages=53–62 |doi=10.4137/CMT.S2313 | doi-access = free }}</ref>
==References==

{{reflist}}
==History==
{{see also|Development of dipeptidyl peptidase-4 inhibitors}}

Sitagliptin was approved by the US ] (FDA) in October 2006,<ref name=FDAapproval>{{cite press release | title = FDA Approves New Treatment for Diabetes | publisher = U.S. ] (FDA) | date = October 17, 2006 | url = https://www.fda.gov/bbs/topics/NEWS/2006/NEW01492.html | archive-url = https://web.archive.org/web/20090228075200/https://www.fda.gov/bbs/topics/NEWS/2006/NEW01492.html | archive-date = February 28, 2009 | url-status = dead | access-date = October 17, 2006 }}</ref> and is sold under the brand name Januvia.<ref>{{cite web | title=Drug Approval Package: Januvia (Sitagliptin Phosphate) NDA #021995 | website=U.S. ] (FDA) | url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2006/021995s000TOC.cfm | access-date=September 27, 2024}}</ref> In April 2007, the FDA approved an oral combination of ] sold under the brand name Janumet.<ref>{{cite web | title=Drug Approval Package: Janumet (Sitagliptin/Metformin Hydrochloride) NDA #022044 | website=U.S. ] (FDA) | date=July 8, 2008 | url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2007/022044TOC.cfm | access-date=September 27, 2024}}</ref> In October 2011, the FDA approved an oral combination of ] sold under the brand name Juvisync.<ref>{{cite web | title=Drug Approval Package: Juvisync (sitagliptin and simvastatin fixed-dose combination) Tablets NDA #202343 | website=U.S. ] (FDA) | date=July 13, 2012 | url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2011/202343Orig1s000TOC.cfm | access-date=September 27, 2024}}</ref><ref name=FDAJuvisyncApproval>{{cite press release | title = FDA Approves Combination Therapy Juvisync | publisher = U.S. ] (FDA) | date = October 7, 2011 | url = https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm274748.htm | archive-url = https://web.archive.org/web/20140824195440/https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm274748.htm | archive-date = August 24, 2014 | url-status = dead | access-date = November 17, 2013 }}</ref> The extended release version of sitagliptin/metformin was approved in February 2012.<ref>{{cite web | title=Drug Approval Package: Janumet XR (sitagliptin/metformin hydrochloride) NDA #202270 | website=U.S. ] (FDA) | date=September 3, 2013 | url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2012/202270_janumet_xr_toc.cfm | access-date=September 27, 2024}}</ref>


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==External links== ==External links==
* {{commonscat-inline}}
*

* Merck & Co.
== References ==
*&nbsp;– PubPK
{{reflist}}
* - Merck press release.
* - Forbes.com
* - Forbes.com
* {{UTGlucagon|sitagliptin}}&nbsp;– Sitagliptin
* {{UTGlucagon|dpp4}}&nbsp;– About DPP-4
*


{{Oral hypoglycemics}} {{Oral hypoglycemics}}
{{Merck&Co}} {{Merck&Co}}
{{Portal bar | Medicine}}
{{Authority control}}


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Latest revision as of 14:30, 7 January 2025

Diabetes medication

Pharmaceutical compound
Sitagliptin
Clinical data
Pronunciation/sɪtəˈɡlɪptɪn/
Trade namesJanuvia, Zituvio, others
AHFS/Drugs.comMonograph
MedlinePlusa606023
License data
Pregnancy
category
  • AU: B3
Routes of
administration
By mouth
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability87%
Protein binding38%
MetabolismLiver (CYP3A4- and CYP2C8-mediated)
Elimination half-life8 to 14 h
ExcretionKidney (80%)
Identifiers
IUPAC name
  • (R)-4-oxo-4-triazolopyrazin-7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-amine
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.217.948 Edit this at Wikidata
Chemical and physical data
FormulaC16H15F6N5O
Molar mass407.320 g·mol
3D model (JSmol)
SMILES
  • Fc1cc(c(F)cc1F)C(N)CC(=O)N3Cc2nnc(n2CC3)C(F)(F)F
InChI
  • InChI=1S/C16H15F6N5O/c17-10-6-12(19)11(18)4-8(10)3-9(23)5-14(28)26-1-2-27-13(7-26)24-25-15(27)16(20,21)22/h4,6,9H,1-3,5,7,23H2/t9-/m1/s1
  • Key:MFFMDFFZMYYVKS-SECBINFHSA-N
  (verify)

Sitagliptin, sold under the brand name Januvia among others, is an anti-diabetic medication used to treat type 2 diabetes. In the United Kingdom it is listed as less preferred than metformin or a sulfonylurea. It is taken by mouth. It is also available in the fixed-dose combination medication sitagliptin/metformin (Janumet, Janumet XR).

Common side effects include headaches, swelling of the legs, and upper respiratory tract infections. Serious side effects may include angioedema, low blood sugar, kidney problems, pancreatitis, and joint pain. Whether use in pregnancy or breastfeeding is safe is unclear. It is in the dipeptidyl peptidase-4 (DPP-4) inhibitor class and works by increasing the production of insulin and decreasing the production of glucagon by the pancreas.

Sitagliptin was developed by Merck & Co. and approved for medical use in the United States in 2006. In 2022, it was the 86th most commonly prescribed medication in the United States, with more than 7 million prescriptions. It is available as a generic medication, but not in the United States.

Medical uses

Sitagliptin is used to treat type 2 diabetes. It is generally less preferred than metformin or sulfonylureas. It is taken by mouth. It is also available as the fixed-dose combinations of sitagliptin/metformin (Janumet, Janumet XR) and sitagliptin/simvastatin (Juvisync).

Sitagliptin should not be used to treat type 1 diabetes. In December 2020, the US Food and Drug Administration (FDA) approved labeling changes stating that Januvia (sitagliptin), Janumet (sitagliptin and metformin hydrochloride), and Janumet XR (sitagliptin and metformin hydrochloride extended-release) are not proven to improve glycemic (blood sugar) control in children aged 10 to 17 with type 2 diabetes. The drugs are approved to improve blood sugar control in adults aged 18 and older with type 2 diabetes.

Adverse effects

Adverse effects from sitagliptin are similar to placebo, except for rare nausea, common cold-like symptoms, and photosensitivity. It does not increase the risk of diarrhea. No significant difference exists in the occurrence of hypoglycemia between placebo and sitagliptin. In those taking sulphonylureas, the risk of low blood sugar is increased.

The existence of rare case reports of kidney failure and hypersensitivity reactions is noted in the United States prescribing information, but a causative role for sitagliptin has not been established.

Several postmarketing reports of pancreatitis (some fatal) have been made in people treated with sitagliptin and other DPP-4 inhibitors, and the US FDA package insert carries a warning to this effect, although the causal link between sitagliptin and pancreatitis has not yet been fully substantiated. One study with lab rats published in 2009 concluded that some of the possible risks of pancreatitis or pancreatic cancer may be reduced when it is used with metformin. However, while DPP-4 inhibitors showed an increase in such risk factors, as of 2009, no increase in pancreatic cancer has been reported in individuals taking DPP-4 inhibitors.

In 2015, the US Food and Drug Administration (FDA) added a new warning and precaution about the risk of "severe and disabling" joint pain to the labels of all DPP-4 inhibitor medicines.

Mechanism of action

See also: Dipeptidyl peptidase-4 inhibitors

Sitagliptin works to competitively inhibit the enzyme dipeptidyl peptidase 4 (DPP-4). This enzyme breaks down the incretins GLP-1 and GIP, gastrointestinal hormones released in response to a meal. By preventing breakdown of GLP-1 and GIP, they are able to increase the secretion of insulin and suppress the release of glucagon by the alpha cells of the pancreas. This drives blood glucose levels towards normal. As the blood glucose level approaches normal, the amounts of insulin released and glucagon suppressed diminishes, thus tending to prevent an "overshoot" and subsequent low blood sugar (hypoglycemia), which is seen with some other oral hypoglycemic agents.

Sitagliptin has been shown to lower HbA1c level by about 0.7% points versus placebo. It is slightly less effective than metformin when used as a monotherapy. It does not cause weight gain and has less hypoglycemia compared to sulfonylureas. Sitagliptin is recommended as a second-line drug (in combination with other drugs) after the combination of diet/exercise and metformin fails.

History

See also: Development of dipeptidyl peptidase-4 inhibitors

Sitagliptin was approved by the US Food and Drug Administration (FDA) in October 2006, and is sold under the brand name Januvia. In April 2007, the FDA approved an oral combination of sitagliptin/metformin sold under the brand name Janumet. In October 2011, the FDA approved an oral combination of sitagliptin/simvastatin sold under the brand name Juvisync. The extended release version of sitagliptin/metformin was approved in February 2012.

External links

References

  1. "Product monograph brand safety updates". Health Canada. February 2024. Retrieved March 24, 2024.
  2. ^ "Januvia- sitagliptin tablet, film coated". DailyMed. Archived from the original on October 27, 2021. Retrieved October 15, 2021.
  3. "Zituvio- sitagliptin tablet". DailyMed. November 1, 2023. Retrieved December 25, 2023.
  4. "Zituvio- sitagliptin tablet". DailyMed. November 1, 2023. Retrieved December 25, 2023.
  5. "Januvia EPAR". European Medicines Agency. September 17, 2018. Archived from the original on October 23, 2021. Retrieved October 15, 2021.
  6. "Xelevia EPAR". European Medicines Agency (EMA). March 21, 2007. Retrieved October 19, 2024.
  7. ^ Herman GA, Stevens C, van Dyck K, Bergman A, Yi B, De Smet M, et al. (December 2005). "Pharmacokinetics and pharmacodynamics of sitagliptin, an inhibitor of dipeptidyl peptidase IV, in healthy subjects: results from two randomized, double-blind, placebo-controlled studies with single oral doses". Clinical Pharmacology and Therapeutics. 78 (6): 675–688. doi:10.1016/j.clpt.2005.09.002. PMID 16338283. S2CID 20935646.{{cite journal}}: CS1 maint: overridden setting (link)
  8. ^ "Sitagliptin Monograph for Professionals". Drugs.com. American Society of Health-System Pharmacists. Archived from the original on March 4, 2016. Retrieved March 3, 2019.
  9. ^ British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 681. ISBN 9780857113382.
  10. "Sitagliptin Pregnancy and Breastfeeding Warnings". Drugs.com. Archived from the original on March 6, 2019. Retrieved March 3, 2019.
  11. "The Top 300 of 2022". ClinCalc. Archived from the original on August 30, 2024. Retrieved August 30, 2024.
  12. "Sitagliptin Drug Usage Statistics, United States, 2013 - 2022". ClinCalc. Retrieved August 30, 2024.
  13. "Generic Januvia Availability". Drugs.com. Retrieved December 1, 2023.
  14. "JAMP Pharma Group receives Health Canada approval for PrJAMP Sitagliptin, a new generic alternative for the treatment of type 2 diabetes" (Press release). JAMP Pharma. January 6, 2023. Retrieved June 19, 2023 – via Newswire.
  15. "Sitagliptin SUN EPAR". European Medicines Agency (EMA). December 9, 2021. Retrieved September 27, 2024.
  16. ^ "FDA Approves Combination Therapy Juvisync" (Press release). U.S. Food and Drug Administration (FDA). October 7, 2011. Archived from the original on August 24, 2014. Retrieved November 17, 2013.
  17. ^ "Diabetes drug not proven to improve blood sugar in pediatric patients". U.S. Food and Drug Administration (FDA). December 4, 2020. Archived from the original on December 4, 2020. Retrieved December 5, 2020. Public Domain This article incorporates text from this source, which is in the public domain.
  18. ^ "Januvia Side Effects & Drug Interactions". RxList.com. 2007. Archived from the original on November 20, 2007. Retrieved November 28, 2007.
  19. Zhao Q, Hong D, Zheng D, Xiao Y, Wu B (2014). "Risk of diarrhea in patients with type 2 diabetes mellitus treated with sitagliptin: a meta-analysis of 30 randomized clinical trials". Drug Design, Development and Therapy. 8: 2283–2294. doi:10.2147/DDDT.S70945. PMC 4234286. PMID 25419118.
  20. Stricklin SM, Stoecker WV, Rader RK, Hood AF, Litt JZ, Schuman TP (February 2012). "Persistent edematous-plaque photosensitivity observed with sitagliptin phosphate (Januvia®)". Dermatology Online Journal. 18 (2): 9. doi:10.5070/D30D70K7B2. PMID 22398230. Archived from the original on April 8, 2019. Retrieved June 6, 2019.
  21. "Januvia side effect: Photosensitivity reaction - eHealthMe". www.ehealthme.com. Archived from the original on June 7, 2019. Retrieved June 6, 2019.
  22. Salvo F, Moore N, Arnaud M, Robinson P, Raschi E, De Ponti F, et al. (May 2016). "Addition of dipeptidyl peptidase-4 inhibitors to sulphonylureas and risk of hypoglycaemia: systematic review and meta-analysis". BMJ. 353: i2231. doi:10.1136/bmj.i2231. PMC 4854021. PMID 27142267.{{cite journal}}: CS1 maint: overridden setting (link)
  23. Olansky L (January 2010). "Do incretin-based therapies cause acute pancreatitis?". Journal of Diabetes Science and Technology. 4 (1): 228–229. doi:10.1177/193229681000400129. PMC 2825646. PMID 20167189.
  24. "FDA Drug Safety Communication: FDA investigating reports of possible increased risk of pancreatitis and pre-cancerous findings of the pancreas from incretin mimetic drugs for type 2 diabetes". U.S. Food and Drug Administration (FDA). June 21, 2019. Archived from the original on May 10, 2022. Retrieved May 10, 2022.
  25. National Prescribing Service (August 2010). "Sitagliptin for Type 2 Diabetes". Archived from the original on July 18, 2010. Retrieved August 27, 2010.
  26. Matveyenko AV, Dry S, Cox HI, Moshtaghian A, Gurlo T, Galasso R, et al. (July 2009). "Beneficial endocrine but adverse exocrine effects of sitagliptin in the human islet amyloid polypeptide transgenic rat model of type 2 diabetes: interactions with metformin". Diabetes. 58 (7): 1604–1615. doi:10.2337/db09-0058. PMC 2699878. PMID 19403868.{{cite journal}}: CS1 maint: overridden setting (link)
  27. "DPP-4 Inhibitors for Type 2 Diabetes: Drug Safety Communication—May Cause Severe Joint Pain". U.S. Food and Drug Administration (FDA). August 28, 2015. Archived from the original on December 13, 2019. Retrieved September 1, 2015.
  28. Herman GA, Bergman A, Liu F, Stevens C, Wang AQ, Zeng W, et al. (August 2006). "Pharmacokinetics and pharmacodynamic effects of the oral DPP-4 inhibitor sitagliptin in middle-aged obese subjects". Journal of Clinical Pharmacology. 46 (8): 876–886. doi:10.1177/0091270006289850. PMID 16855072. S2CID 45849328.{{cite journal}}: CS1 maint: overridden setting (link)
  29. Gadsby R (2009). "Efficacy and Safety of Sitagliptin in the Treatment of Type 2 Diabetes". Clinical Medicine: Therapeutics. 1 (1): 53–62. doi:10.4137/CMT.S2313.
  30. "FDA Approves New Treatment for Diabetes" (Press release). U.S. Food and Drug Administration (FDA). October 17, 2006. Archived from the original on February 28, 2009. Retrieved October 17, 2006.
  31. "Drug Approval Package: Januvia (Sitagliptin Phosphate) NDA #021995". U.S. Food and Drug Administration (FDA). Retrieved September 27, 2024.
  32. "Drug Approval Package: Janumet (Sitagliptin/Metformin Hydrochloride) NDA #022044". U.S. Food and Drug Administration (FDA). July 8, 2008. Retrieved September 27, 2024.
  33. "Drug Approval Package: Juvisync (sitagliptin and simvastatin fixed-dose combination) Tablets NDA #202343". U.S. Food and Drug Administration (FDA). July 13, 2012. Retrieved September 27, 2024.
  34. "Drug Approval Package: Janumet XR (sitagliptin/metformin hydrochloride) NDA #202270". U.S. Food and Drug Administration (FDA). September 3, 2013. Retrieved September 27, 2024.
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