Generic Attruby Availability
Last updated on Apr 10, 2025.
Attruby is a brand name of acoramidis, approved by the FDA in the following formulation(s):
ATTRUBY (acoramidis hydrochloride - tablet;oral)
-
Manufacturer: BRIDGEBIO PHARMA
Approval date: November 22, 2024
Strength(s): EQ 356MG BASE [RLD]
Is there a generic version of Attruby available?
No. There is currently no therapeutically equivalent version of Attruby available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Attruby. 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.
-
Compounds and compositions that bind and stabilize transthyretin and their use for inhibiting transthyretin amyloidosis and protein-protein interactions
Patent 10,398,681
Issued: September 3, 2019
Inventor(s): Graef; Isabella A. et al.
Assignee(s): The Board of Trustees of the Leland Stanford Junior University (Stanford, CA)Disclosed herein are compounds and compositions thereof which find use in increasing stability of proteins particularly proteins that tend to misfold and form aggregates. Also provided herein are methods for using these compounds and compositions for increasing stability of proteins and thereby decreasing aggregate formation by these proteins. Also disclosed herein are heterobifunctional compounds that include a TTR binding compound connected to a targeting moiety via a linker, for use in disrupting PPIs of a target protein.
Patent expiration dates:
- May 5, 2031✓
- May 5, 2031
-
Process for preparing AG-10, its intermediates, and salts thereof
Patent 10,513,497
Issued: December 24, 2019
Inventor(s): Chand; Pooran et al.
Assignee(s): EIDOS THERAPEUTICS, INC. (San Francisco, CA)Provided herein are improved processes for the preparation of a compound of Formula IX (AG-10). Also provided herein are pharmaceutically acceptable salts of Formula I and Formula Ib ##STR00001##
as well as crystalline types of Formula IX (AG-10). The processes described herein provide improved yields and efficiency, while the pharmaceutically acceptable salts and crystalline forms provide unexpected pharmacokinetic properties. Other features and aspects of the present disclosure will be apparent to a person of skill in the art upon reading the remainder of the specification.Patent expiration dates:
- February 16, 2038✓
- February 16, 2038
-
Compounds and compositions that bind and stabilize transthyretin and their use for inhibiting transthyretin amyloidosis and protein-protein interactions
Patent 10,842,777
Issued: November 24, 2020
Inventor(s): Graef; Isabella A. et al.
Assignee(s): The Board of Trustees of the Leland Stanford Junior University (Stanford, CA)Disclosed herein are compounds and compositions thereof which find use in increasing stability of proteins particularly proteins that tend to misfold and form aggregates. Also provided herein are methods for using these compounds and compositions for increasing stability of proteins and thereby decreasing aggregate formation by these proteins. Also disclosed herein are heterobifunctional compounds that include a TTR binding compound connected to a targeting moiety via a linker, for use in disrupting PPIs of a target protein.
Patent expiration dates:
- May 5, 2031✓
- May 5, 2031
-
Methods of treating TTR amyloidosis using AG10
Patent 11,058,668
Issued: July 13, 2021
Inventor(s): Sinha; Uma et al.
Assignee(s): EIDOS THERAPEUTICS, INC. (San Francisco, CA)Described herein are methods for treating transthyretin (TTR) amyloidosis in a subject. The methods include specific dosing regimens that have great efficacy in treating the subjects and that are well tolerated in subjects.
Patent expiration dates:
- March 22, 2039✓
- March 22, 2039
-
Formulations of AG10
Patent 11,260,047
Issued: March 1, 2022
Inventor(s): Jernelius; Jesper et al.
Assignee(s): EIDOS THERAPEUTICS, INC. (San Francisco, CA)The present disclosure provides high-load tablet formulations of AG10 or a pharmaceutically acceptable salt thereof. In some aspects, provided herein are table formulations of AG10 or a pharmaceutically acceptable salt thereof that include at least 40% or more AG10 by weight and at least one pharmaceutical excipient selected from one or more fillers, one or more binders, one or more disintegrants, and one or more lubricants.
Patent expiration dates:
- August 16, 2039✓
- August 16, 2039
-
Processes for preparing AG-10, its intermediates, and salts thereof
Patent 11,919,865
Issued: March 5, 2024
Inventor(s): Chand; Pooran et al.
Assignee(s): EIDOS THERAPEUTICS, INC. (San Francisco, CA)Provided herein are improved processes for the preparation of a compound of Formula IX (AG-10). Also provided herein are pharmaceutically acceptable salts of Formula I and Formula Ib ##STR00001##
as well as crystalline types of Formula IX (AG-10). The processes described herein provide improved yields and efficiency, while the pharmaceutically acceptable salts and crystalline forms provide unexpected pharmacokinetic properties. Other features and aspects of the present disclosure will be apparent to a person of skill in the art upon reading the remainder of the specification.Patent expiration dates:
- February 16, 2038✓
- February 16, 2038
-
Formulations of AG10
Patent 12,005,043
Issued: June 11, 2024
Inventor(s): Jernelius; Jesper et al.
Assignee(s): EIDOS THERAPEUTICS, INC. (Palo Alto, CA)The present disclosure provides high-load tablet formulations of AG10 or a pharmaceutically acceptable salt thereof. In some aspects, provided herein are table formulations of AG10 or a pharmaceutically acceptable salt thereof that include at least 40% or more AG10 by weight and at least one pharmaceutical excipient selected from one or more fillers, one or more binders, one or more disintegrants, and one or more lubricants.
Patent expiration dates:
- August 16, 2039✓✓
- August 16, 2039
-
Methods of treating TTR amyloidosis using AG10
Patent 12,070,449
Issued: August 27, 2024
Inventor(s): Sinha; Uma et al.
Assignee(s): EIDOS THERAPEUTICS, INC. (Palo Alto, CA)Described herein are methods for treating transthyretin (TTR) amyloidosis in a subject. The methods include specific dosing regimens that have great efficacy in treating the subjects and that are well tolerated in subjects
Patent expiration dates:
- March 22, 2039✓
- March 22, 2039
-
Identification of stabilizers of multimeric proteins
Patent 8,877,795
Issued: November 4, 2014
Inventor(s): Graef; Isabella A. et al.
Assignee(s): The Board of Trustees of the Leland Stanford Junior University (Palo Alto, CA)Disclosed herein are compounds and compositions thereof which find use in increasing stability of TTR tetramers reducing its tendency to misfold and form aggregates. Also provided herein are methods for using these compounds and compositions for increasing stability of TTR and thereby decreasing aggregate formation by TTR. Also disclosed herein are methods to screen for candidate compounds that increase stability of TTR. Also disclosed herein are heterobifunctional compounds that include a TTR binding compound connected to a targeting moiety via a linker, for use in disrupting PPIs of a target protein.
Patent expiration dates:
- May 5, 2031✓
- May 5, 2031
-
Compounds and compositions that bind and stabilize transthyretin and their use for inhibiting transthyretin amyloidosis and protein-protein interactions
Patent 9,169,214
Issued: October 27, 2015
Inventor(s): Graef; Isabella A. et al.
Assignee(s): The Board of Trustees of the Leland Stanford Junior University (Palo Alto, CA)Disclosed herein are compounds and compositions thereof which find use in increasing stability of proteins particularly proteins that tend to misfold and form aggregates. Also provided herein are methods for using these compounds and compositions for increasing stability of proteins and thereby decreasing aggregate formation by these proteins. Also disclosed herein are heterobifunctional compounds that include a TTR binding compound connected to a targeting moiety via a linker, for use in disrupting PPIs of a target protein.
Patent expiration dates:
- May 5, 2031✓✓
- May 5, 2031
-
Compounds and compositions that bind and stabilize transthyretin and their use for inhibiting transthyretin amyloidosis and protein-protein interactions
Patent 9,642,838
Issued: May 9, 2017
Inventor(s): Graef; Isabella A. et al.
Assignee(s): The Board of Trustees of the Leland Standford Junior University (Palo Alto, CA)Disclosed herein are compounds and compositions thereof which find use in increasing stability of proteins particularly proteins that tend to misfold and form aggregates. Also provided herein are methods for using these compounds and compositions for increasing stability of proteins and thereby decreasing aggregate formation by these proteins. Also disclosed herein are heterobifunctional compounds that include a TTR binding compound connected to a targeting moiety via a linker, for use in disrupting PPIs of a target protein.
Patent expiration dates:
- May 5, 2031✓✓
- May 5, 2031
-
Compounds and compositions that bind and stabilize transthyretin and their use for inhibiting transthyretin amyloidosis and protein-protein interactions
Patent 9,913,826
Issued: March 13, 2018
Inventor(s): Graef; Isabella A. et al.
Assignee(s): The Board of Trustees of the Leland Stanford Junior University (Stanford, CA)Disclosed herein are compounds and compositions thereof which find use in increasing stability of proteins particularly proteins that tend to misfold and form aggregates. Also provided herein are methods for using these compounds and compositions for increasing stability of proteins and thereby decreasing aggregate formation by these proteins. Also disclosed herein are heterobifunctional compounds that include a TTR binding compound connected to a targeting moiety via a linker, for use in disrupting PPIs of a target protein.
Patent expiration dates:
- May 5, 2031✓
- May 5, 2031
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 22, 2029 - NEW CHEMICAL ENTITY
- November 22, 2031 - TREATMENT OF THE CARDIOMYOPATHY OF WILD-TYPE OR VARIANT TRANSTHYRETIN-MEDIATED AMYLOIDOSIS(ATTR-CM) IN ADULTS TO REDUCE CARDIOVASCULAR DEATH AND CARDIOVASCULAR-RELATED HOSPITALIZATION
More about Attruby (acoramidis)
- Check interactions
- Compare alternatives
- Pricing & coupons
- Drug images
- Side effects
- Dosage information
- During pregnancy
- FDA approval history
- Drug class: transthyretin stabilizers
- Breastfeeding
- En español
Patient resources
Professional resources
Related treatment guides
Glossary
Term | Definition |
---|---|
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
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.