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Generic Genvoya Availability

Genvoya is a brand name of cobicistat/elvitegravir/emtricitabine/tenofovir alafenamide, approved by the FDA in the following formulation(s):

GENVOYA (cobicistat; elvitegravir; emtricitabine; tenofovir alafenamide fumarate - tablet;oral)

  • Manufacturer: GILEAD SCIENCES INC
    Approval date: November 5, 2015
    Strength(s): 150MG;150MG;200MG;EQ 10MG BASE [RLD]

Has a generic version of Genvoya been approved?

No. There is currently no therapeutically equivalent version of Genvoya available in the United States.

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Genvoya. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.

Related Patents

Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.

  • Method for the synthesis, compositions and use of 2'-deoxy-5-fluoro-3'-thiacytidine and related compounds
    Patent 5,814,639
    Issued: September 29, 1998
    Inventor(s): Liotta; Dennis C. & Schinazi; Raymond F. & Choi; Woo-Baeg
    Assignee(s): Emory University
    The present invention relates to a method of preparing the antiviral compounds 2'-deoxy-5-fluoro-3'thiacytidine (FTC) and various prodrug analogues of FTC from inexpensive precursors with the option of introducing functionality as needed; methods of using these compounds, particularly in the prevention and treatment of AIDS; and the compounds themselves. This synthetic route allows the stereoselective preparation of the biologically active isomer of these compounds and related compounds.
    Patent expiration dates:
    • September 29, 2015
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      Drug product
    • March 29, 2016
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      Pediatric exclusivity
  • Antiviral activity and resolution of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane
    Patent 5,914,331
    Issued: June 22, 1999
    Inventor(s): Liotta; Dennis C. & Schinazi; Raymond F. & Choi; Woo-Baeg
    Assignee(s): Emory University
    A method and composition for the treatment of HIV and HBV infections in humans is disclosed that includes administering an effective amount of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane, a pharmaceutically acceptable derivative thereof, including a 5' or N.sup.4 alkylated or acylated derivative, or a pharmaceutically acceptable salt thereof, in a pharmaceutically acceptable carrier. A process for the resolution of a racemic mixture of nucleoside enantiomers is also disclosed that includes the step of exposing the racemic mixture to an enzyme that preferentially catalyzes a reaction in one of the enantiomers.
    Patent expiration dates:
    • July 2, 2017
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      Drug substance
    • January 2, 2018
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      Pediatric exclusivity
  • Antiviral activity and resolution of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane
    Patent 6,642,245
    Issued: November 4, 2003
    Inventor(s): Dennis C.; Liotta & Raymond F.; Schinazi & Woo-Baeg; Choi
    Assignee(s): Emory University
    A method and composition for the treatment of HIV and HBV infections in humans is disclosed that includes administering an effective amount of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane, a pharmaceutically acceptable derivative thereof, including a 5′ or N4 alkylated or acylated derivative, or a pharmaceutically acceptable salt thereof, in a pharmaceutically acceptable carrier. A process for the resolution of a racemic mixture of nucleoside enantiomers is also disclosed that includes the step of exposing the racemic mixture to an enzyme that preferentially catalyzes a reaction in one of the enantiomers.
    Patent expiration dates:
    • November 4, 2020
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      Patent use: TREATMENT OF HIV INFECTION
    • May 4, 2021
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      Pediatric exclusivity
  • Method of resolution and antiviral activity of 1,3-oxathiolane nuclesoside enantiomers
    Patent 6,703,396
    Issued: March 9, 2004
    Inventor(s): Dennis C.; Liotta & Raymond F.; Schinazi & Woo-Baeg; Choi
    Assignee(s): Emory University
    A process for the resolution of a racemic mixture of nucleoside enantiomers that includes the step of exposing the racemic mixture to an enzyme that preferentially catalyzes a reaction in one of the enantiomers. The nucleoside enantiomer (−)-2-hydroxymethyl-5-(5-flurocytosin-1-yl)-1,3-oxathiolane is an effective antiviral agent against HIV, HBV, and other viruses replicating in a similar manner.
    Patent expiration dates:
    • March 9, 2021
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      Drug substance
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      Drug product
    • September 9, 2021
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      Pediatric exclusivity
  • 4-oxoquinoline compound and use thereof as pharmaceutical agent
    Patent 7,176,220
    Issued: February 13, 2007
    Inventor(s): Satoh; Motohide & Kawakami; Hiroshi & Itoh; Yoshiharu & Shinkai; Hisashi & Motomura; Takahisa & Aramaki; Hisateru & Matsuzaki; Yuji & Watanabe; Wataru & Wamaki; Shuichi
    Assignee(s): Japan Tobacco Inc.
    An anti-HIV agent containing, as an active ingredient, a 4-oxoquinoline compound represented by the following formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable salt thereof. The compound of the present invention has HIV integrase inhibitory action and is useful as an anti-HIV agent for the prophylaxis or therapy of AIDS. Moreover, by a combined use with other anti-HIV agents such as protease inhibitors, reverse transcriptase inhibitors and the like, the compound can become a more effective anti-HIV agent. Since the compound has high inhibitory activity specific for integrases, it can provide a safe pharmaceutical agent with a fewer side effects for human.
    Patent expiration dates:
    • November 20, 2023
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      Patent use: TREATMENT OF HIV INFECTION
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  • Prodrugs of phosphonate nucleotide analogues
    Patent 7,390,791
    Issued: June 24, 2008
    Inventor(s): Becker; Mark W. & Chapman; Harlan H. & Cihlar; Tomas & Eisenberg; Eugene J. & He; Gong-Xin & Kernan; Michael R. & Lee; William A. & Prisbe; Ernest J. & Rohloff; John C. & Sparacino; Mark L.
    Assignee(s): Gilead Sciences, Inc.
    A novel method has led to the identification of novel mixed ester-amidates of PMPA for retroviral or hepadnaviral therapy, including compounds of structure (5a) having substituent groups as defined herein. Compositions of these novel compounds in pharmaceutically acceptable excipients and their use in therapy and prophylaxis are provided.
    Patent expiration dates:
    • May 7, 2022
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  • Stable crystal of 4-oxoquinoline compound
    Patent 7,635,704
    Issued: December 22, 2009
    Inventor(s): Satoh; Motohide & Motomura; Takahisa & Matsuda; Takashi & Kondo; Kentaro & Ando; Koji & Matsuda; Koji & Miyake; Shuji & Uehara; Hideto
    Assignee(s): Japan Tobacco Inc.
    Provision of a stabilized crystal of 6-(3-chloro-2-fluorobenzyl)-1-[(S)-1-hydroxymethyl-2-methylpropyl]-7-methoxy-4-oxo-1, 4-dihydroquinoline-3-carboxylic acid (compound A). A crystal of compound A, which shows a particular X-ray powder diffraction pattern of a characteristic diffraction peaks at diffraction angles 2θ(°) as measured by X-ray powder diffractmetry.
    Patent expiration dates:
    • October 26, 2026
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      Patent use: TREATMENT OF HIV INFECTION
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      Drug product
  • Prodrugs of phosphonate nucoleotide analogues
    Patent 7,803,788
    Issued: September 28, 2010
    Inventor(s): Becker; Mark W. & Chapman; Harlan H. & Cihlar; Tomas & Eisenberg; Eugene J. & He; Gong-Xin & Kernan; Michael R. & Lee; William A. & Prisbe; Ernest J. & Rohloff; John C. & Sparacino; Mark L.
    Assignee(s): Gilead Sciences, Inc.
    A novel method has led to the identification of novel mixed ester-amidates of PMPA for retroviral or hepadnaviral therapy, including compounds of structure (5a) having substituent groups as defined herein. Compositions of these novel compounds in pharmaceutically acceptable excipients and their use in therapy and prophylaxis are provided.
    Patent expiration dates:
    • February 2, 2022
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      Patent use: TREATMENT OF HIV INFECTION
  • Modulators of pharmacokinetic properties of therapeutics
    Patent 8,148,374
    Issued: April 3, 2012
    Inventor(s): Desai; Manoj C. & Liu; Hongtao & Xu; Lianhong
    Assignee(s): Gilead Sciences, Inc.
    The present application provides for a compound of Formula IV, or a pharmaceutically acceptable salt, solvate, and/or ester thereof, compositions containing such compounds, therapeutic methods that include the administration of such compounds, and therapeutic methods and include the administration of such compounds with at least one additional therapeutic agent.
    Patent expiration dates:
    • September 3, 2029
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      Patent use: TREATMENT OF HIV INFECTION USING A COMPOSITION CONTAINING A PHARMACOKNIETIC ENHANCER THAT INHIBITS CYTOCHROME P450 MONOOXYGENASE
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  • Combination therapy
    Patent 8,633,219
    Issued: January 21, 2014
    Assignee(s): Japan Tobacco Inc.
    The present invention relates to a combination therapy for treating an HIV infection or inhibiting integrase comprising (S)-6-(3-Chloro-2-fluorobenzyl)-1-(1-hydroxymethyl-2-methylpropyl)-7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (“Compound A”) or a pharmaceutically acceptable solvate or salt thereof in combination with at least one other anti-HIV agent. In some embodiments of the present invention, the other anti-HIV agents are chosen from reverse transcriptase inhibitors and protease inhibitors. In certain embodiments of the present invention, the other anti-HIV agents are chosen from AZT, 3TC, PMPA, efavirenz, indinavir, nelfinavir, a combination of AZT/3TC, and a combination of PMPA/3TC. Since Compound A has a high inhibitory activity specific for integrases, when used in combinations with other anti-HIV agents it can provide a combination therapy with fewer side effects for humans.
    Patent expiration dates:
    • April 24, 2030
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      Patent use: TREATMENT OF HIV INFECTION
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      Drug product
  • Tenofovir alafenamide hemifumarate
    Patent 8,754,065
    Issued: June 17, 2014
    Assignee(s): Gilead Sciences, Inc.
    A hemifumarate form of 9-[(R)-2-[[(S)-[[(S)-1-(isopropoxycarbonyl)ethyl]amino]phenoxyphosphinyl]methoxy]propyl]adenine (tenofovir alafenamide), and antiviral therapy using tenofovir alafenamide hemifumarate (e.g., anti-HIV and anti-HBV therapies).
    Patent expiration dates:
    • August 15, 2032
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      Patent use: TREATMENT OF HIV INFECTION
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      Drug substance
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      Drug product
  • Stable crystal of 4-oxoquinoline compound
    Patent 8,981,103
    Issued: March 17, 2015
    Assignee(s): Japan Tobacco Inc.
    Provision of a stabilized crystal of 6-(3-chloro-2-fluorobenzyl)-1-[(S)-1-hydroxymethyl-2-methylpropyl]-7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (compound A). A crystal of compound A, which shows a particular X-ray powder diffraction pattern of a characteristic diffraction peaks at diffraction angles 2θ(°) as measured by X-ray powder diffractometry.
    Patent expiration dates:
    • October 26, 2026
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      Drug substance
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      Drug product
  • Tenofovir alafenamide hemifumarate
    Patent 9,296,769
    Issued: March 29, 2016
    Assignee(s): Gilead Sciences, Inc.
    A hemifumarate form of 9-[(R)-2-[[(S)-[[(S)-1-(isopropoxycarbonyl)ethyl]amino]phenoxyphosphinyl]methoxy]propyl]adenine (tenofovir alafenamide), and antiviral therapy using tenofovir alafenamide hemifumarate (e.g., anti-HIV and anti-HBV therapies).
    Patent expiration dates:
    • August 15, 2032
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      Patent use: TREATMENT OF HIV INFECTION
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      Drug substance
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      Drug product

Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • November 5, 2020 - NEW CHEMICAL ENTITY

Glossary

TermDefinition
Drug PatentA drug patent is assigned by the U.S. Patent and Trademark Office and assigns exclusive legal right to the patent holder to protect the proprietary chemical formulation. The patent assigns exclusive legal right to the inventor or patent holder, and may include entities such as the drug brand name, trademark, product dosage form, ingredient formulation, or manufacturing process A patent usually expires 20 years from the date of filing, but can be variable based on many factors, including development of new formulations of the original chemical, and patent infringement litigation.
Drug ExclusivityExclusivity is the sole marketing rights granted by the FDA to a manufacturer upon the approval of a drug and may run simultaneously with a patent. Exclusivity periods can run from 180 days to seven years depending upon the circumstance of the exclusivity grant.
RLDA Reference Listed Drug (RLD) is an approved drug product to which new generic versions are compared to show that they are bioequivalent. A drug company seeking approval to market a generic equivalent must refer to the Reference Listed Drug in its Abbreviated New Drug Application (ANDA). By designating a single reference listed drug as the standard to which all generic versions must be shown to be bioequivalent, FDA hopes to avoid possible significant variations among generic drugs and their brand name counterpart.
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