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{{Short description|NSAID analgesic and anti-inflammatory drug}}
{{Drugbox {{Drugbox
| Verifiedfields = changed
| verifiedrevid = 444024277
| Watchedfields = changed
| IUPAC_name = 2-amino-3-benzoylbenzeneacetamide
| verifiedrevid = 447808600
| image = Nepafenac-2D-skeletal.png
| image = Nepafenac-2D-skeletal.svg
| alt =


<!--Clinical data--> <!--Clinical data-->
| tradename = | tradename = Nevanac, Ilevro, Amnac, others
| Drugs.com = {{drugs.com|monograph|nepafenac}} | Drugs.com = {{drugs.com|monograph|nepafenac}}
| MedlinePlus = a606007 | MedlinePlus = a606007
| DailyMedID = Nepafenac
| pregnancy_category = C
| pregnancy_AU = C
| pregnancy_AU_comment = <ref name="Drugs.com pregnancy">{{cite web | title=Nepafenac ophthalmic Use During Pregnancy | website=Drugs.com | date=6 June 2019 | url=https://www.drugs.com/pregnancy/nepafenac-ophthalmic.html | access-date=13 September 2020}}</ref>
| licence_EU = yes
| legal_AU = S4
| legal_AU_comment = <ref>{{cite web | title=Prescription medicines: registration of new chemical entities in Australia, 2015 | website=Therapeutic Goods Administration (TGA) | date=21 June 2022 | url=https://www.tga.gov.au/prescription-medicines-registration-new-chemical-entities-australia-2015 | access-date=10 April 2023}}</ref>
| legal_US = Rx-only | legal_US = Rx-only
| legal_status = | legal_status = Rx-only
| routes_of_administration = ] | routes_of_administration = ]
| ATC_prefix = S01
| ATC_suffix = BC10
| ATC_supplemental =


<!--Pharmacokinetic data--> <!--Pharmacokinetic data-->
| bioavailability = | bioavailability =
| protein_bound = | protein_bound =
| metabolism = | metabolism =
| elimination_half-life = | elimination_half-life =


<!--Identifiers--> <!--Identifiers-->
| CAS_number_Ref = {{cascite|correct|CAS}}
| CAS_number =
| CAS_number = 78281-72-8
| ATC_prefix = S01
| ATC_suffix = BC10
| ATC_supplemental =
| PubChem = 151075 | PubChem = 151075
| IUPHAR_ligand = 7564
| DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank = DB06802 | DrugBank = DB06802
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| KEGG_Ref = {{keggcite|correct|kegg}} | KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = D05143 | KEGG = D05143
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 75922
| ChEMBL_Ref = {{ebicite|correct|EBI}} | ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 1021 | ChEMBL = 1021


<!--Chemical data--> <!--Chemical data-->
| IUPAC_name = 2-amino-3-benzoylbenzeneacetamide
| C=15 | H=14 | N=2 | O=2
| C=15 | H=14 | N=2 | O=2
| molecular_weight = 254.28 ]/]
| smiles = O=C(c1cccc(c1N)CC(=O)N)c2ccccc2 | SMILES = O=C(c1cccc(c1N)CC(=O)N)c2ccccc2
| InChI = 1/C15H14N2O2/c16-13(18)9-11-7-4-8-12(14(11)17)15(19)10-5-2-1-3-6-10/h1-8H,9,17H2,(H2,16,18)
| InChIKey = QEFAQIPZVLVERP-UHFFFAOYAP
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C15H14N2O2/c16-13(18)9-11-7-4-8-12(14(11)17)15(19)10-5-2-1-3-6-10/h1-8H,9,17H2,(H2,16,18) | StdInChI = 1S/C15H14N2O2/c16-13(18)9-11-7-4-8-12(14(11)17)15(19)10-5-2-1-3-6-10/h1-8H,9,17H2,(H2,16,18)
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}} }}


'''Nepafenac''' is a ] (NSAID), usually sold as a ] ] (0.1% solution. Nepafenac is manufactured by ] as '''Nevanac'''. It is used to treat pain and inflammation associated with cataract surgery. '''Nepafenac''', sold under the brand name '''Nevanac''' among others, is a ] (NSAID), usually sold as a ] ] 0.1% solution (Nevanac) or 0.3% solution (Ilevro). It is used to treat pain and inflammation associated with ] surgery.<ref name="Drugs.com">Nepafenac {{drugs.com|monograph|nepafenac}}</ref> Nepafenac is a ] of ], an inhibitor of ] and ] activity.<ref>Drugbank: </ref><ref>{{cite journal | vauthors = Zanetti FR, Fulco EA, Chaves FR, da Costa Pinto AP, Arieta CE, Lira RP | title = Effect of preoperative use of topical prednisolone acetate, ketorolac tromethamine, nepafenac and placebo, on the maintenance of intraoperative mydriasis during cataract surgery: a randomized trial | journal = Indian Journal of Ophthalmology | volume = 60 | issue = 4 | pages = 277–81 | date = July 2012 | pmid = 22824596 | pmc = 3442462 | doi = 10.4103/0301-4738.98705 | doi-access = free }}</ref>

==Medical uses==

Nepafenac is indicated for use in the treatment of pain and inflammation following cataract surgery.<ref name = "Drugs.com" /><ref name="Nevanac Package Insert">{{cite web | title=Nevanac- nepafenac suspension/ drops | website=DailyMed | date=9 September 2019 | url=https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3ad48650-75e3-4c74-9302-01b0088f164e | access-date=6 July 2020}}</ref><ref name="Ilevro Package Insert">{{cite web | title=Ilevro- nepafenac suspension | website=DailyMed | date=9 September 2019 | url=https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6c212466-ff8d-ecfc-ede2-ef8bdcaaf114 | access-date=6 July 2020}}</ref><ref name="Nevanac EPAR" />

In the European Union nepafenac is also indicated for the reduction in the risk of postoperative ] associated with cataract surgery in people with diabetes.<ref name="Nevanac EPAR">{{cite web | title=Nevanac EPAR | website=] (EMA) | date=17 September 2018 | url=https://www.ema.europa.eu/en/medicines/human/EPAR/nevanac | access-date=6 July 2020}}</ref>

==Pharmacology==

===Mechanism of action===

Nepafenac is an NSAID, thought to be a prodrug of amfenac after conversion by ocular tissue hydrolases after penetration via the ].<ref name ="Nevanac Package Insert" /><ref name = "Ilevro Package Insert" /> Amfenac, like other NSAIDs, is thought to inhibit ] action.<ref name ="Nevanac Package Insert" /><ref name = "Ilevro Package Insert" />

==Adverse events==

] include headache; runny nose; pain or pressure in the face; nausea; vomiting; and dry, itchy, sticky eyes.<ref name="Medline Nepafenac">{{cite web|title=Nepafenac Ophthalmic|url=https://medlineplus.gov/druginfo/meds/a606007.html|website=MedlinePlus|publisher=U.S. National Library of Medicine|access-date=October 31, 2017}}</ref> Serious side effects include red or bloody eyes; foreign body sensation in the eye; sensitivity to light; decreased ]; seeing specks or spots; teary eyes; or eye discharge or crusting.<ref name = "Medline Nepafenac" />

==Regulatory==

===Nevanac===

On February 25, 2005, Alcon filed a ] (NDA) with the U.S. ] (FDA) for Nevanac 0.1%.<ref name="Nevanac Approval">{{cite web|title=Nevanac Approval Package|url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2005/021862s000_Nevanac_approv.pdf|website=U.S. ] (FDA)|access-date=October 31, 2017}}</ref> Results from the two trials referenced in the NDA (Phase 2/3 study C-02-53; Phase 3 study C-03-32) have not been published.<ref name="Topical Opthalmic NSAIDS">{{cite journal | vauthors = Gaynes BI, Onyekwuluje A | title = Topical ophthalmic NSAIDs: a discussion with focus on nepafenac ophthalmic suspension | journal = Clinical Ophthalmology | volume = 2 | issue = 2 | pages = 355–68 | date = June 2008 | pmid = 19668727 | pmc = 2693998 | doi = 10.2147/opth.s1067 | doi-access = free }}</ref> Study C-02-53 consisted of 228 patients across 10 centers in the United States.<ref name="Nevanac Stat Review">{{cite web|title=Nevanac Statistical Review|url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2005/021862s000_Nevanac_statr.pdf|website=U.S. ] (FDA)|access-date=October 31, 2017}}</ref> Study C-03-32 consisted of 522 patients across 22 centers in the United States.<ref name = "Nevanac Stat Review" /> The efficacy results presented were confirmed in a study published in 2007.<ref>{{cite journal | vauthors = Lane SS, Modi SS, Lehmann RP, Holland EJ | title = Nepafenac ophthalmic suspension 0.1% for the prevention and treatment of ocular inflammation associated with cataract surgery | journal = Journal of Cataract and Refractive Surgery | volume = 33 | issue = 1 | pages = 53–8 | date = January 2007 | pmid = 17189793 | doi = 10.1016/j.jcrs.2006.08.043 | s2cid = 38881826 }}</ref>

Nevanac was approved by the FDA on August 19, 2005, with application number 021–862.<ref name="Nevanac DAP">{{cite web|title=Drug Approval Package: Nevanac (Nepafenac) Ophthalmic Suspension NDA #021862|url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2005/021862s000_NevanacTOC.cfm|website=U.S. ] (FDA)|access-date=October 27, 2017|date=January 6, 2005 }}</ref>

===Ilevro===

An NDA for Ilevro was filed on December 15, 2011.<ref name="Ilevro Approval">{{cite web|title=Ilevro Approval Package|url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2012/203491Orig1s000Approv.pdf|website=U.S. ] (FDA)|access-date=October 31, 2017}}</ref> In a one-month study, no new toxicities arose in the new formulation of nepafenac.<ref name="Ilevro PC Review">{{cite web|title=203491 Pharmacology Review|url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2012/203491Orig1s000PharmR.pdf|website=U.S. ] (FDA)|access-date=October 31, 2017}}</ref> Safety and efficacy information was derived from the previous Nevanac application.<ref name = "Ilevro PC Review" /> In June 2010, a confirmatory study began (Study C09055) consisting of over 2000 patients from 49 US sites and 37 European sites.<ref name="Ilevro Stat Review">{{cite web|title=Ilevro Statistical Review|url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2012/203491Orig1s000StatR.pdf|website=U.S. ] (FDA)|access-date=October 31, 2017}}</ref><ref name="Ilevro CT 1">{{cite journal|title=Confirmatory Study Nepafenac 0.3%|url=https://clinicaltrials.gov/ct2/show/NCT01109173|website=ClinicalTrials.gov|date=29 November 2012 |publisher=U.S. National Library of Medicine|access-date=October 31, 2017}}</ref> A second phase 3 trial (Study C11003) was conducted in a population of 1,342 patients at 37 sites across the United States which failed to demonstrate superiority over Nevanac in an altered dosing regimen.<ref name = "Ilevro Stat Review" />

Ilevro was approved by the FDA on October 16, 2012, with application number 203–491.<ref name="Ilevro DAP">{{cite web|title=Drug Approval Package: Nepafenac Ophthalmic Suspension, 0.3% NDA #203491|url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2012/203491_nepafenac_toc.cfm|website=U.S. ] (FDA)|access-date=October 27, 2017|date=April 8, 2013}}</ref>

==Commercialization==

Both Nevanac and Ilevro are manufactured and sold by ], Inc.<ref name = "Nevanac Package Insert" /><ref name = "Ilevro Package Insert" /> Alcon is currently a division of ] International AG, which is primarily based out of Switzerland.<ref name="Novartis About Us">{{cite web|title=About Us|url=https://www.novartis.com/about-us|website=Novartis|access-date=October 27, 2017}}</ref> Alcon, Inc. also holds locations in both Switzerland and the United States.<ref name="Nevanac Correspondence">{{cite web|title=Nevanac Administrative Documents and Correspondence|url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2005/021862s000_Nevanac_admincorres.pdf|website=U.S. ] (FDA)|access-date=October 27, 2017}}</ref> The company has gone through several name changes, from Alcon Laboratories, Inc. to Alcon Universal, Ltd., to Alcon, Inc.<ref name = "Nevanac Correspondence" />

Nevanac entered the market in 2005 as a product of Alcon, at the time a subsidiary of Nestlé.<ref name="Alcon 2010 20F">{{cite web|title=Alcon Annual Report 2010|url=https://www.sec.gov/Archives/edgar/data/1167379/000116737911000037/acl20f2010.pdf|website=SEC EDGAR|publisher=United States Securities and Exchange Commission|access-date=October 30, 2017}}</ref> On April 6, 2008, Novartis agreed to purchase approximately 74 million shares of Alcon from Nestlé at $143.18 per share.<ref name = "Alcon 2010 20F" /> On January 4, 2010, Novartis agreed to purchase all remaining shares of Alcon from Nestlé, totalling 156 million shares or 77% of the shares in the company.<ref name = "Alcon 2010 20F" /> At the time of the purchase, a proposal for a merger under Swiss merger law was given to the Alcon board of directors.<ref name = "Alcon 2010 20F" /> The merger was agreed upon on December 15, 2010, making Alcon "the second largest division within Novartis."<ref name = "Alcon 2010 20F" /> The merger was completed on April 8, 2011.<ref name="Alcon Form 15">{{cite web|title=Alcon Form 15|url=https://www.sec.gov/Archives/edgar/data/1167379/000110465911021611/a11-7954_41512b.htm|website=SEC EDGAR|publisher=United States Securities and Exchange Commission|access-date=October 30, 2017}}</ref>

Ilevro was launched by Alcon on January 21, 2013.<ref name="Ilevro Launch">{{cite web|title=Alcon Launches ILEVRO™ (nepafenac ophthalmic suspension) 0.3%, a New Non-Steroidal Anti-Inflammatory Drug, for the Treatment of Pain and Inflammation Associated with Cataract Surgery|url=https://www.alcon.com/news/media-releases/alcon-launches-ilevro-nepafenac-ophthalmic-suspension-03-new-non-steroidal-anti|website=Alcon|access-date=October 30, 2017|archive-date=December 15, 2018|archive-url=https://web.archive.org/web/20181215122150/https://www.alcon.com/news/media-releases/alcon-launches-ilevro-nepafenac-ophthalmic-suspension-03-new-non-steroidal-anti|url-status=dead}}</ref> In 2014 and 2015, net sales by Alcon grew, contributed to in part by the increased volume in sales of Ilevro.<ref name="2013 20F">{{cite web|title=Form 20-F|url=https://www.sec.gov/Archives/edgar/data/1114448/000104746914000415/a2217883z20-f.htm|website=SEC EDGAR|publisher=United States Securities and Exchange Commission|access-date=October 30, 2017}}</ref><ref name="2014 20F">{{cite web|title=Form 20-F|url=https://www.sec.gov/Archives/edgar/data/1114448/000104746915000433/a2222787z20-f.htm|website=SEC EDGAR|publisher=United States Securities and Exchange Commission|access-date=October 30, 2017}}</ref><ref name="2015 20F">{{cite web|title=Form 20F|url=https://www.sec.gov/Archives/edgar/data/1114448/000104746916009872/a2227040z20-f.htm|website=SEC EDGAR|publisher=United States Securities and Exchange Commission|access-date=October 30, 2017}}</ref> That financial year, Novartis reported $18 billion in total financial debt.<ref name = "2013 20F" /> That figure has grown steadily since. In 2016, Novartis reported a total debt of $23.8 billion,<ref name="2016 20F">{{cite web|title=Form 20-F|url=https://www.sec.gov/Archives/edgar/data/1114448/000104746917000338/a2230622z20-f.htm|website=SEC EDGAR|publisher=United States Securities and Exchange Commission|access-date=October 31, 2017}}</ref> up from the $21.9 billion reported in 2015 <ref name = "2015 20F" /> and the $20.4 billion reported in 2014.<ref name = "2014 20F" /> As of May 2017, Novartis is estimated to be worth $193.2 billion.<ref name="Novartis Forbes">{{cite web|title=Novartis on the Forbes Top Multinational Performers List|url=https://www.forbes.com/companies/novartis/|website=Forbes|access-date=October 31, 2017}}</ref>

On January 27, 2016, Alcon was moved to become a branch of the Innovative Medicines Division at Novartis.<ref name = "2016 20F" /> Early in 2016, Alcon formed agreements with both TrueVision and PowerVision, and acquired Transcend Medical.<ref name = "2016 20F" /> As of January 2017, Novartis is weighing options for Alcon in the business structure.<ref name = "2016 20F" />

===Commercial risks===

Alcon faced declining growth in 2016, having faced challenges in development and marketing of new products.<ref name = "2016 20F" />

===Marketing===

Novartis maintains a detailing unit geared toward health professionals consisting of over 3,000 employees within the United States and an additional 21,000 worldwide.<ref name = "2016 20F" /> Novartis is also seeking to expand direct-to-consumer advertising and entrance into specialty product markets.<ref name = "2016 20F" /> Novartis also notes the influence of position and preference on US Centers for Medicare & Medicaid formularies in expanding their market value.<ref name = "2016 20F" />

Nepafenac, Nevanac, and Ilevro are all absent from the 2016 Annual Report issued from Novartis.<ref name = "2016 20F" />

===Intellectual property===

There are currently{{when|date=July 2020}} seven U.S. patents filed that are directly associated with the modernized formulations of nepafenac, all stemming from Novartis.<ref name="PharmaCompass">{{cite web|title=Nepafenac|url=https://www.pharmacompass.com/patent-expiry-expiration/nepafenac|website=U.S. Patents|publisher=PharmaCompass|access-date=October 30, 2017}}</ref> There are three patents associated with Nevanac that are still{{when|date=July 2020}} active<ref name="Nevanac Patent Count">{{cite web|title=Generic Nevanac Availability|url=https://www.drugs.com/availability/generic-nevanac.html|website=Drugs.com|access-date=October 31, 2017}}</ref> and four associated with Ilevro.<ref name="Ilevro Patent Count">{{cite web|title=Generic Ilevro Availability|url=https://www.drugs.com/availability/generic-ilevro.html|website=Drugs.com|access-date=October 31, 2017}}</ref> The earliest patent related to the modern formulations of nepafenac was approved on June 11, 2002, after being filed in 1999, by Bahram Asgharian.<ref name="Asgharian Patent">{{cite web|title=United States Patent Application: 6403609|url=http://patft.uspto.gov/netacgi/nph-Parser?Sect2=PTO1&Sect2=HITOFF&p=1&u=/netahtml/PTO/search-bool.html&r=1&f=G&l=50&d=PALL&RefSrch=yes&Query=PN/6403609|website=United States Patent and Trademark Office|access-date=October 31, 2017}}</ref> A patent was filed by Warren Wong, associated with Alcon, Inc. based out of ], on December 2, 2005, for aqueous suspensions of nepafenac.<ref name="Wong Nepafenac PTO">{{cite web|title=United States Patent Application: 0060122277|url=http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=/netahtml/PTO/srchnum.html&r=1&f=G&l=50&s1=20060122277.PGNR.|website=United States Patent and Trademark Office|access-date=October 30, 2017}}</ref> Another patent for a nepafenac-based drug was filed on May 8, 2006, by Geoffrey Owen, Amy Brooks, and Gustav Graff.<ref name="Nepafenac PTO">{{cite web|title=United States Patent Application: 0060257487|url=http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=/netahtml/PTO/srchnum.html&r=1&f=G&l=50&s1=20060257487.PGNR.|website=United States Patent and Trademark Office|access-date=October 27, 2017}}</ref> A patent was filed by Masood A. Chowhan and Huagang Chen on February 9, 2007, and approved on May 24, 2011,<ref name="Chowhan Chen Patent">{{cite web|title=United States Patent: 7947295|url=http://patft.uspto.gov/netacgi/nph-Parser?Sect2=PTO1&Sect2=HITOFF&p=1&u=/netahtml/PTO/search-bool.html&r=1&f=G&l=50&d=PALL&RefSrch=yes&Query=PN/7947295|website=United States Patent and Trademark Office|access-date=October 31, 2017}}</ref> followed closely by a patent filed by Warren Wong on September 23, 2010, and approved on December 6, 2011.<ref name="Wong Patent 2">{{cite web|title=United States Patent: 8071648|url=http://patft.uspto.gov/netacgi/nph-Parser?Sect2=PTO1&Sect2=HITOFF&p=1&u=/netahtml/PTO/search-bool.html&r=1&f=G&l=50&d=PALL&RefSrch=yes&Query=PN/8071648|website=United States Patent and Trademark Office|access-date=October 31, 2017}}</ref> Masood A. Chowhan, Malay Ghosh, Bahram Asgharian, and Wesley Wehsin Han filed another patent on December 1, 2010, and approved on December 30, 2014.<ref name="Chowhan et al Patent">{{cite web|title=United States Patent: 8921337|url=http://patft.uspto.gov/netacgi/nph-Parser?Sect2=PTO1&Sect2=HITOFF&p=1&u=/netahtml/PTO/search-bool.html&r=1&f=G&l=50&d=PALL&RefSrch=yes&Query=PN/8921337|website=United States Patent and Trademark Office|access-date=October 31, 2017}}</ref> The most recent{{when|date=July 2020}} patent was filed by Masood A. Chowhan, Malay Ghosh, Bahram Asgharian, and Wesley Weshin Han on November 12, 2014, and approved on May 30, 2017.<ref name="Chowhan et. al. 2">{{cite web|title=United States Patent: 9662398|url=http://patft.uspto.gov/netacgi/nph-Parser?Sect2=PTO1&Sect2=HITOFF&p=1&u=/netahtml/PTO/search-bool.html&r=1&f=G&l=50&d=PALL&RefSrch=yes&Query=PN/9662398|website=United States Patent and Trademark Office|access-date=October 31, 2017}}</ref> These patents are in effect until dates ranging between July 17, 2018, and March 31, 2032.<ref name = "Ilevro Patent Count" />


Novartis also maintains patents on nepafenac in 26 countries outside the United States.<ref name="Worldwide Patent Count">{{cite web|title=Nepafenac - Generic Drug Details|url=https://www.drugpatentwatch.com/p/generic-api/nepafenac|website=DrugPatentWatch|publisher=thinkBiotech LLC|access-date=October 31, 2017}}</ref>
The usual dose is 1 drop in each affected eye beginning 1 day prior to cataract surgery, continued on the day of surgery and through the first 2 weeks of the postoperative period.


== References ==
Its ] may include decreased visual acuity, a feeling that something is in the eye, increased eye pressure or a sticky sensation, as well as other effects.
{{reflist}}


== External links == == External links ==
* {{cite web | url = https://druginfo.nlm.nih.gov/drugportal/name/nepafenac | publisher = U.S. National Library of Medicine | work = Drug Information Portal | title = Nepafenac }}
*


{{NSAIDs}} {{NSAIDs}}
{{Portal bar | Medicine}}


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Latest revision as of 08:12, 1 November 2024

NSAID analgesic and anti-inflammatory drug Pharmaceutical compound
Nepafenac
Clinical data
Trade namesNevanac, Ilevro, Amnac, others
AHFS/Drugs.comMonograph
MedlinePlusa606007
License data
Pregnancy
category
  • AU: C
Routes of
administration
Topical eye drops
ATC code
Legal status
Legal status
  • AU: S4 (Prescription only)
  • US: ℞-only
  • In general: ℞ (Prescription only)
Identifiers
IUPAC name
  • 2-amino-3-benzoylbenzeneacetamide
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.207.414 Edit this at Wikidata
Chemical and physical data
FormulaC15H14N2O2
Molar mass254.289 g·mol
3D model (JSmol)
SMILES
  • O=C(c1cccc(c1N)CC(=O)N)c2ccccc2
InChI
  • InChI=1S/C15H14N2O2/c16-13(18)9-11-7-4-8-12(14(11)17)15(19)10-5-2-1-3-6-10/h1-8H,9,17H2,(H2,16,18)
  • Key:QEFAQIPZVLVERP-UHFFFAOYSA-N
  (what is this?)  (verify)

Nepafenac, sold under the brand name Nevanac among others, is a nonsteroidal anti-inflammatory drug (NSAID), usually sold as a prescription eye drop 0.1% solution (Nevanac) or 0.3% solution (Ilevro). It is used to treat pain and inflammation associated with cataract surgery. Nepafenac is a prodrug of amfenac, an inhibitor of COX-1 and COX-2 activity.

Medical uses

Nepafenac is indicated for use in the treatment of pain and inflammation following cataract surgery.

In the European Union nepafenac is also indicated for the reduction in the risk of postoperative macular edema associated with cataract surgery in people with diabetes.

Pharmacology

Mechanism of action

Nepafenac is an NSAID, thought to be a prodrug of amfenac after conversion by ocular tissue hydrolases after penetration via the cornea. Amfenac, like other NSAIDs, is thought to inhibit cyclooxygenase action.

Adverse events

Side effects include headache; runny nose; pain or pressure in the face; nausea; vomiting; and dry, itchy, sticky eyes. Serious side effects include red or bloody eyes; foreign body sensation in the eye; sensitivity to light; decreased visual acuity; seeing specks or spots; teary eyes; or eye discharge or crusting.

Regulatory

Nevanac

On February 25, 2005, Alcon filed a New Drug Application (NDA) with the U.S. Food and Drug Administration (FDA) for Nevanac 0.1%. Results from the two trials referenced in the NDA (Phase 2/3 study C-02-53; Phase 3 study C-03-32) have not been published. Study C-02-53 consisted of 228 patients across 10 centers in the United States. Study C-03-32 consisted of 522 patients across 22 centers in the United States. The efficacy results presented were confirmed in a study published in 2007.

Nevanac was approved by the FDA on August 19, 2005, with application number 021–862.

Ilevro

An NDA for Ilevro was filed on December 15, 2011. In a one-month study, no new toxicities arose in the new formulation of nepafenac. Safety and efficacy information was derived from the previous Nevanac application. In June 2010, a confirmatory study began (Study C09055) consisting of over 2000 patients from 49 US sites and 37 European sites. A second phase 3 trial (Study C11003) was conducted in a population of 1,342 patients at 37 sites across the United States which failed to demonstrate superiority over Nevanac in an altered dosing regimen.

Ilevro was approved by the FDA on October 16, 2012, with application number 203–491.

Commercialization

Both Nevanac and Ilevro are manufactured and sold by Alcon, Inc. Alcon is currently a division of Novartis International AG, which is primarily based out of Switzerland. Alcon, Inc. also holds locations in both Switzerland and the United States. The company has gone through several name changes, from Alcon Laboratories, Inc. to Alcon Universal, Ltd., to Alcon, Inc.

Nevanac entered the market in 2005 as a product of Alcon, at the time a subsidiary of Nestlé. On April 6, 2008, Novartis agreed to purchase approximately 74 million shares of Alcon from Nestlé at $143.18 per share. On January 4, 2010, Novartis agreed to purchase all remaining shares of Alcon from Nestlé, totalling 156 million shares or 77% of the shares in the company. At the time of the purchase, a proposal for a merger under Swiss merger law was given to the Alcon board of directors. The merger was agreed upon on December 15, 2010, making Alcon "the second largest division within Novartis." The merger was completed on April 8, 2011.

Ilevro was launched by Alcon on January 21, 2013. In 2014 and 2015, net sales by Alcon grew, contributed to in part by the increased volume in sales of Ilevro. That financial year, Novartis reported $18 billion in total financial debt. That figure has grown steadily since. In 2016, Novartis reported a total debt of $23.8 billion, up from the $21.9 billion reported in 2015 and the $20.4 billion reported in 2014. As of May 2017, Novartis is estimated to be worth $193.2 billion.

On January 27, 2016, Alcon was moved to become a branch of the Innovative Medicines Division at Novartis. Early in 2016, Alcon formed agreements with both TrueVision and PowerVision, and acquired Transcend Medical. As of January 2017, Novartis is weighing options for Alcon in the business structure.

Commercial risks

Alcon faced declining growth in 2016, having faced challenges in development and marketing of new products.

Marketing

Novartis maintains a detailing unit geared toward health professionals consisting of over 3,000 employees within the United States and an additional 21,000 worldwide. Novartis is also seeking to expand direct-to-consumer advertising and entrance into specialty product markets. Novartis also notes the influence of position and preference on US Centers for Medicare & Medicaid formularies in expanding their market value.

Nepafenac, Nevanac, and Ilevro are all absent from the 2016 Annual Report issued from Novartis.

Intellectual property

There are currently seven U.S. patents filed that are directly associated with the modernized formulations of nepafenac, all stemming from Novartis. There are three patents associated with Nevanac that are still active and four associated with Ilevro. The earliest patent related to the modern formulations of nepafenac was approved on June 11, 2002, after being filed in 1999, by Bahram Asgharian. A patent was filed by Warren Wong, associated with Alcon, Inc. based out of Fort Worth, Texas, on December 2, 2005, for aqueous suspensions of nepafenac. Another patent for a nepafenac-based drug was filed on May 8, 2006, by Geoffrey Owen, Amy Brooks, and Gustav Graff. A patent was filed by Masood A. Chowhan and Huagang Chen on February 9, 2007, and approved on May 24, 2011, followed closely by a patent filed by Warren Wong on September 23, 2010, and approved on December 6, 2011. Masood A. Chowhan, Malay Ghosh, Bahram Asgharian, and Wesley Wehsin Han filed another patent on December 1, 2010, and approved on December 30, 2014. The most recent patent was filed by Masood A. Chowhan, Malay Ghosh, Bahram Asgharian, and Wesley Weshin Han on November 12, 2014, and approved on May 30, 2017. These patents are in effect until dates ranging between July 17, 2018, and March 31, 2032.

Novartis also maintains patents on nepafenac in 26 countries outside the United States.

References

  1. "Nepafenac ophthalmic Use During Pregnancy". Drugs.com. 6 June 2019. Retrieved 13 September 2020.
  2. "Prescription medicines: registration of new chemical entities in Australia, 2015". Therapeutic Goods Administration (TGA). 21 June 2022. Retrieved 10 April 2023.
  3. ^ Nepafenac Monograph
  4. Drugbank: Nepafenac
  5. Zanetti FR, Fulco EA, Chaves FR, da Costa Pinto AP, Arieta CE, Lira RP (July 2012). "Effect of preoperative use of topical prednisolone acetate, ketorolac tromethamine, nepafenac and placebo, on the maintenance of intraoperative mydriasis during cataract surgery: a randomized trial". Indian Journal of Ophthalmology. 60 (4): 277–81. doi:10.4103/0301-4738.98705. PMC 3442462. PMID 22824596.
  6. ^ "Nevanac- nepafenac suspension/ drops". DailyMed. 9 September 2019. Retrieved 6 July 2020.
  7. ^ "Ilevro- nepafenac suspension". DailyMed. 9 September 2019. Retrieved 6 July 2020.
  8. ^ "Nevanac EPAR". European Medicines Agency (EMA). 17 September 2018. Retrieved 6 July 2020.
  9. ^ "Nepafenac Ophthalmic". MedlinePlus. U.S. National Library of Medicine. Retrieved October 31, 2017.
  10. "Nevanac Approval Package" (PDF). U.S. Food and Drug Administration (FDA). Retrieved October 31, 2017.
  11. Gaynes BI, Onyekwuluje A (June 2008). "Topical ophthalmic NSAIDs: a discussion with focus on nepafenac ophthalmic suspension". Clinical Ophthalmology. 2 (2): 355–68. doi:10.2147/opth.s1067. PMC 2693998. PMID 19668727.
  12. ^ "Nevanac Statistical Review" (PDF). U.S. Food and Drug Administration (FDA). Retrieved October 31, 2017.
  13. Lane SS, Modi SS, Lehmann RP, Holland EJ (January 2007). "Nepafenac ophthalmic suspension 0.1% for the prevention and treatment of ocular inflammation associated with cataract surgery". Journal of Cataract and Refractive Surgery. 33 (1): 53–8. doi:10.1016/j.jcrs.2006.08.043. PMID 17189793. S2CID 38881826.
  14. "Drug Approval Package: Nevanac (Nepafenac) Ophthalmic Suspension NDA #021862". U.S. Food and Drug Administration (FDA). January 6, 2005. Retrieved October 27, 2017.
  15. "Ilevro Approval Package" (PDF). U.S. Food and Drug Administration (FDA). Retrieved October 31, 2017.
  16. ^ "203491 Pharmacology Review" (PDF). U.S. Food and Drug Administration (FDA). Retrieved October 31, 2017.
  17. ^ "Ilevro Statistical Review" (PDF). U.S. Food and Drug Administration (FDA). Retrieved October 31, 2017.
  18. "Confirmatory Study Nepafenac 0.3%". ClinicalTrials.gov. U.S. National Library of Medicine. 29 November 2012. Retrieved October 31, 2017.
  19. "Drug Approval Package: Nepafenac Ophthalmic Suspension, 0.3% NDA #203491". U.S. Food and Drug Administration (FDA). April 8, 2013. Retrieved October 27, 2017.
  20. "About Us". Novartis. Retrieved October 27, 2017.
  21. ^ "Nevanac Administrative Documents and Correspondence" (PDF). U.S. Food and Drug Administration (FDA). Retrieved October 27, 2017.
  22. ^ "Alcon Annual Report 2010" (PDF). SEC EDGAR. United States Securities and Exchange Commission. Retrieved October 30, 2017.
  23. "Alcon Form 15". SEC EDGAR. United States Securities and Exchange Commission. Retrieved October 30, 2017.
  24. "Alcon Launches ILEVRO™ (nepafenac ophthalmic suspension) 0.3%, a New Non-Steroidal Anti-Inflammatory Drug, for the Treatment of Pain and Inflammation Associated with Cataract Surgery". Alcon. Archived from the original on December 15, 2018. Retrieved October 30, 2017.
  25. ^ "Form 20-F". SEC EDGAR. United States Securities and Exchange Commission. Retrieved October 30, 2017.
  26. ^ "Form 20-F". SEC EDGAR. United States Securities and Exchange Commission. Retrieved October 30, 2017.
  27. ^ "Form 20F". SEC EDGAR. United States Securities and Exchange Commission. Retrieved October 30, 2017.
  28. ^ "Form 20-F". SEC EDGAR. United States Securities and Exchange Commission. Retrieved October 31, 2017.
  29. "Novartis on the Forbes Top Multinational Performers List". Forbes. Retrieved October 31, 2017.
  30. "Nepafenac". U.S. Patents. PharmaCompass. Retrieved October 30, 2017.
  31. "Generic Nevanac Availability". Drugs.com. Retrieved October 31, 2017.
  32. ^ "Generic Ilevro Availability". Drugs.com. Retrieved October 31, 2017.
  33. "United States Patent Application: 6403609". United States Patent and Trademark Office. Retrieved October 31, 2017.
  34. "United States Patent Application: 0060122277". United States Patent and Trademark Office. Retrieved October 30, 2017.
  35. "United States Patent Application: 0060257487". United States Patent and Trademark Office. Retrieved October 27, 2017.
  36. "United States Patent: 7947295". United States Patent and Trademark Office. Retrieved October 31, 2017.
  37. "United States Patent: 8071648". United States Patent and Trademark Office. Retrieved October 31, 2017.
  38. "United States Patent: 8921337". United States Patent and Trademark Office. Retrieved October 31, 2017.
  39. "United States Patent: 9662398". United States Patent and Trademark Office. Retrieved October 31, 2017.
  40. "Nepafenac - Generic Drug Details". DrugPatentWatch. thinkBiotech LLC. Retrieved October 31, 2017.

External links

  • "Nepafenac". Drug Information Portal. U.S. National Library of Medicine.
Non-steroidal anti-inflammatory drugs (NSAIDs) (primarily M01A and M02A, also N02BA)
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