Nepafenac

Nepafenac
Names
Trade namesNevanac, Ilevro, Amnac, others
IUPAC name
  • 2-amino-3-benzoylbenzeneacetamide
Clinical data
Drug classNSAID
Main usesPain and inflammation from cataract surgery[1]
Side effectsIrritation of the eye[1]
Pregnancy
category
  • AU: C[2]
  • US: C (Risk not ruled out)[2]
    Routes of
    use
    Eye drops
    External links
    AHFS/Drugs.comMonograph
    US NLMNepafenac
    MedlinePlusa606007
    Legal
    License data
    Legal status
    • US: ℞-only
    • In general: ℞ (Prescription only)
    Chemical and physical data
    FormulaC15H14N2O2
    Molar mass254.289 g·mol−1
    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) checkY
    • Key:QEFAQIPZVLVERP-UHFFFAOYSA-N checkY

    Nepafenac, sold under the brand name Nevanac among others, is a nonsteroidal anti-inflammatory drug (NSAID) used to treat pain and inflammation associated with cataract surgery.[1] It is used as an eye drop.[1]

    Common side effects include irritation of the eye.[1] Other side effects may include keratitis and hyphema.[3] It works by inhibiting COX-1 and COX-2 and therefore decreasing prostaglandins.[3][1]

    Nepafenac was approved for medical use in the United States in 2005 and Europe in 2007.[3][1] In the United Kingdom a bottle costs the NHS about £15 as of 2021.[4] In the United States this amount costs about 290 USD.[5]

    Medical uses

    Nepafenac is indicated for use in the treatment of pain and inflammation following cataract surgery.[6][7][8][9]

    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.[9]

    Dosage

    It is used once to three times per day depending on the strength of the formulation.[1] It is started once day before the surgery and continued for 2 to 9 weeks.[1]

    Side events

    Side effects include headache; runny nose; pain or pressure in the face; nausea; vomiting; and dry, itchy, sticky eyes.[10] 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.[10]

    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.[7][8] Amfenac, like other NSAIDs, is thought to inhibit cyclooxygenase action.[7][8]

    History

    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%.[11] 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.[12] Study C-02-53 consisted of 228 patients across 10 centers in the United States.[13] Study C-03-32 consisted of 522 patients across 22 centers in the United States.[13] The efficacy results presented were confirmed in a study published in 2007.[14]

    Nevanac was approved by the FDA on August 19, 2005, with application number 021–862.[15]

    Ilevro

    An NDA for Ilevro was filed on December 15, 2011.[16] In a one-month study, no new toxicities arose in the new formulation of nepafenac.[17] Safety and efficacy information was derived from the previous Nevanac application.[17] In June 2010, a confirmatory study began (Study C09055) consisting of over 2000 patients from 49 US sites and 37 European sites.[18][19] 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.[18]

    Ilevro was approved by the FDA on October 16, 2012, with application number 203–491.[20]

    Society and culture

    Cost

    This medication has a cost in Canada of $4.40 (per ml) for 10 ml ilevro oph 0.1 % [21]

    Commercialization

    Both Nevanac and Ilevro are manufactured and sold by Alcon, Inc.[7][8] Alcon is currently a division of Novartis International AG, which is primarily based out of Switzerland.[22] Alcon, Inc. also holds locations in both Switzerland and the United States.[23] The company has gone through several name changes, from Alcon Laboratories, Inc. to Alcon Universal, Ltd., to Alcon, Inc.[23]

    Nevanac entered the market in 2005 as a product of Alcon, at the time a subsidiary of Nestlé.[24] On April 6, 2008, Novartis agreed to purchase approximately 74 million shares of Alcon from Nestlé at $143.18 per share.[24] 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.[24] At the time of the purchase, a proposal for a merger under Swiss merger law was given to the Alcon board of directors.[24] The merger was agreed upon on December 15, 2010, making Alcon "the second largest division within Novartis."[24] The merger was completed on April 8, 2011.[25]

    Ilevro was launched by Alcon on January 21, 2013.[26] In 2014 and 2015, net sales by Alcon grew, contributed to in part by the increased volume in sales of Ilevro.[27][28][29] That financial year, Novartis reported $18 billion in total financial debt.[27] That figure has grown steadily since. In 2016, Novartis reported a total debt of $23.8 billion,[30] up from the $21.9 billion reported in 2015 [29] and the $20.4 billion reported in 2014.[28] As of May 2017, Novartis is estimated to be worth $193.2 billion.[31]

    On January 27, 2016, Alcon was moved to become a branch of the Innovative Medicines Division at Novartis.[30] Early in 2016, Alcon formed agreements with both TrueVision and PowerVision, and acquired Transcend Medical.[30] As of January 2017, Novartis is weighing options for Alcon in the business structure.[30]

    Alcon faced declining growth in 2016, having faced challenges in development and marketing of new products.[30]

    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.[30] Novartis is also seeking to expand direct-to-consumer advertising and entrance into specialty product markets.[30] Novartis also notes the influence of position and preference on US Centers for Medicare & Medicaid formularies in expanding their market value.[30]

    Nepafenac, Nevanac, and Ilevro are all absent from the 2016 Annual Report issued from Novartis.[30]

    Intellectual property

    There are currently seven U.S. patents filed that are directly associated with the modernized formulations of nepafenac, all stemming from Novartis.[32] There are three patents associated with Nevanac that are still active[33] and four associated with Ilevro.[34] The earliest patent related to the modern formulations of nepafenac was approved on June 11, 2002, after being filed in 1999, by Bahram Asgharian.[35] 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.[36] Another patent for a nepafenac-based drug was filed on May 8, 2006, by Geoffrey Owen, Amy Brooks, and Gustav Graff.[37] A patent was filed by Masood A. Chowhan and Huagang Chen on February 9, 2007, and approved on May 24, 2011,[38] followed closely by a patent filed by Warren Wong on September 23, 2010, and approved on December 6, 2011.[39] Masood A. Chowhan, Malay Ghosh, Bahram Asgharian, and Wesley Wehsin Han filed another patent on December 1, 2010, and approved on December 30, 2014.[40] 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.[41] These patents are in effect until dates ranging between July 17, 2018, and March 31, 2032.[34]

    Novartis also maintains patents on nepafenac in 26 countries outside the United States.[42]

    A lawsuit was filed by Alcon on March 4, 2016, against Watson Laboratories in Delaware for the manufacture of a generic version of the 0.3% nepafenac formulation, Ilevro.[43] The complaint was amended on June 14, 2017.[44]

    References

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