Generic Cobenfy Availability
Last updated on Jul 9, 2025.
Cobenfy is a brand name of trospium/xanomeline, approved by the FDA in the following formulation(s):
COBENFY (trospium chloride; xanomeline tartrate - capsule;oral)
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Manufacturer: BRISTOL-MYERS
Approval date: September 26, 2024
Strength(s): 20MG;EQ 50MG BASE [RLD], 20MG;EQ 100MG BASE [RLD], 30MG;EQ 125MG BASE [RLD]
Is there a generic version of Cobenfy available?
No. There is currently no therapeutically equivalent version of Cobenfy available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Cobenfy. 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: Generic Drug FAQ.
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.
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Methods and compositions for treatment of disorders ameliorated by muscarinic receptor activation
Patent 10,238,643
Issued: March 26, 2019
Inventor(s): Elenko; Eric et al.
Assignee(s): PureTech Health LLC (Boston, MA)Methods for the treatment of CNS disorders using combinations of muscarinic activators and inhibitors, and medicaments comprising muscarinic activators and inhibitors.
Patent expiration dates:
- July 21, 2030✓
- July 21, 2030
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Methods and compositions for treatment of disorders ameliorated by muscarinic receptor activation
Patent 10,265,311
Issued: April 23, 2019
Inventor(s): Elenko; Eric et al.
Assignee(s): PureTech Health LLC (Boston, MA)Methods for the treatment of CNS disorders using combinations of muscarinic activators and inhibitors, and medicaments comprising muscarinic activators and inhibitors.
Patent expiration dates:
- July 21, 2030✓
- July 21, 2030
-
Methods and compositions for treatment of disorders ameliorated by muscarinic receptor activation
Patent 10,369,143
Issued: August 6, 2019
Inventor(s): Elenko; Eric et al.
Assignee(s): PureTech Health LLC (Boston, MA)Provided herein is a method of treating a central nervous system disorder in a patient in need thereof, wherein the central nervous system disorder is selected from schizophrenia, Alzheimer's disease, Huntington's disease, Parkinson's disease, and Lewy Body dementia. The method comprises orally administering an initial dose of between 75 mg and 300 mg xanomeline and an initial dose of between 20 mg and 200 mg trospium chloride to the patient during a 24-hour period. Provided that the patient tolerates said administration, an increased dose of trospium chloride and an increased dose of xanomeline are orally administering to the patient, wherein the increased dose of trospium chloride is greater than the initial dose of the trospium chloride, and wherein the increased dose of xanomeline is greater than the initial dose of the xanomeline.
Patent expiration dates:
- July 21, 2030✓
- July 21, 2030
-
Methods and compositions for treatment of disorders ameliorated by muscarinic receptor activation
Patent 10,369,144
Issued: August 6, 2019
Inventor(s): Elenko; Eric et al.
Assignee(s): PureTech Health LLC (Boston, MA)The present disclosure provides a method of treating a central nervous system disorder in a patient in need thereof. The method comprises orally administering between 75 mg and 300 mg xanomeline and between 20 mg and 200 mg trospium chloride to the patient during a 24-hour period. The central nervous system disorder is selected from schizophrenia, Alzheimer's disease, Huntington's disease, Parkinson's disease, and Lewy Body dementia, wherein use of the trospium chloride alleviates a side effect associated with use of the xanomeline.
Patent expiration dates:
- July 21, 2030✓✓
- July 21, 2030
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Methods and compositions for treatment of disorders ameliorated by muscarinic receptor activation
Patent 10,695,339
Issued: June 30, 2020
Inventor(s): Elenko; Eric et al.
Assignee(s): PureTech Health LLC (Boston, MA)The present disclosure provides a method of treating a central nervous system disorder in a patient in need thereof. The method comprises orally administering between 75 mg and 300 mg xanomeline salt and between 20 mg and 200 mg trospium chloride to the patient during a 24-hour period, the central nervous system disorder being selected from schizophrenia, Alzheimer's disease, Huntington's disease, Parkinson's disease, and Lewy Body dementia, wherein use of the trospium chloride alleviates a side effect associated with use of the xanomeline salt.
Patent expiration dates:
- July 21, 2030✓
- July 21, 2030
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Compositions and methods for treatment of disorders ameliorated by muscarinic receptor activation
Patent 10,925,832
Issued: February 23, 2021
Inventor(s): Betancourt; Aimesther et al.
Assignee(s): Karuna Therapeutics, Inc. (Boston, MA)Provided herein is an oral pharmaceutical composition, comprising a plurality of xanomeline beads having a core comprising xanomeline or a salt thereof; and a plurality of trospium beads having a core comprising a salt of trospium.
Patent expiration dates:
- September 27, 2039✓
- September 27, 2039
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Compositions and methods for treating disorders ameliorated by muscarinic receptor activation
Patent 10,933,020
Issued: March 2, 2021
Inventor(s): Betancourt; Aimesther et al.
Assignee(s): Karuna Therapeutics, Inc. (Boston, MA)Provided herein is an oral pharmaceutical composition, comprising a plurality of xanomeline beads having a core comprising xanomeline or a salt thereof, and a plurality of trospium beads having a core comprising a salt of trospium.
Patent expiration dates:
- September 27, 2039✓✓
- September 27, 2039
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Compositions and methods for treating disorders ameliorated by muscarinic receptor activation
Patent 11,452,692
Issued: September 27, 2022
Inventor(s): Betancourt; Aimesther et al.
Assignee(s): Karuna Therapeutics, Inc. (Boston, MA)Provided herein is an oral pharmaceutical composition, comprising a plurality of xanomeline beads having a core comprising xanomeline or a salt thereof; and a plurality of trospium beads having a core comprising a salt of trospium.
Patent expiration dates:
- September 27, 2039✓
- September 27, 2039
-
Compositions and methods for treating disorders ameliorated by muscarinic receptor activation
Patent 11,471,413
Issued: October 18, 2022
Inventor(s): Betancourt; Aimesther et al.
Assignee(s): Karuna Therapeutics, Inc. (Boston, MA)Provided herein is an oral pharmaceutical composition, comprising a plurality of xanomeline beads having a core comprising xanomeline or a salt thereof; and a plurality of trospium beads having a core comprising a salt of trospium.
Patent expiration dates:
- September 27, 2039✓
- September 27, 2039
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Compositions and methods for treating disorders ameliorated by muscarinic receptor activation
Patent 11,890,378
Issued: February 6, 2024
Inventor(s): Betancourt; Aimesther et al.
Assignee(s): Karuna Therapeutics, Inc. (Boston, MA)Provided herein is an oral pharmaceutical composition, comprising a plurality of xanomeline beads having a core comprising xanomeline or a salt thereof; and a plurality of trospium beads having a core comprising a salt of trospium.
Patent expiration dates:
- September 27, 2039✓✓
- September 27, 2039
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:
- September 26, 2029 - NEW CHEMICAL ENTITY
More about Cobenfy (trospium / xanomeline)
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- Reviews (7)
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- Side effects
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- During pregnancy
- FDA approval history
- Drug class: psychotherapeutic combinations
- En español
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Glossary
Term | Definition |
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Drug Patent | A 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 Exclusivity | Exclusivity 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. |
RLD | A 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. |
Further information
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