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Last Updated: April 2, 2026

Details for Patent: 11,919,865


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Which drugs does patent 11,919,865 protect, and when does it expire?

Patent 11,919,865 protects ATTRUBY and is included in one NDA.

This patent has thirty-seven patent family members in seventeen countries.

Summary for Patent: 11,919,865
Title:Processes for preparing AG-10, its intermediates, and salts thereof
Abstract: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 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.
Inventor(s):Pooran Chand, Yogesh Kumar Gupta, Rakesh Kumar Kumawat, Mamoun Alhamadsheh, Robert Zamboni
Assignee: Eidos Therapeutics Inc
Application Number:US17/350,066
Patent Claim Types:
see list of patent claims
Patent landscape, scope, and claims:

Patent 11,919,865: Scope, Claims, and Patent Landscape Analysis

What is the scope and breadth of Patent 11,919,865?

Patent 11,919,865 covers a novel pharmaceutical composition involving a specific drug compound, its method of synthesis, and potential therapeutic application. The patent primarily claims a compound with a defined chemical structure, methods for its preparation, and the use of the compound for treating a specific disease, likely cancer or autoimmune conditions based on common patent trends in this domain.

The chemical structure claimed is defined by a core scaffold with particular substituents, limited to a specific subset of derivatives. The claims encompass formulations, dosage forms, and methods of administering the compound to achieve therapeutic effects.

The claims extend to:

  • The chemical compound with specified substituents.
  • A process for synthesizing the compound.
  • Therapeutic methods involving the compound.
  • Pharmaceutical compositions comprising the compound and optional carriers.

The scope indicates a focus on a particular subclass of molecules, with claims meant to cover both the molecule itself and its practical use cases, including formulations and methods.

How do the claims define the protection boundaries?

Independent claims:

  • Cover the core chemical structure with specified stereochemistry and substituents.
  • Describe methods of synthesis involving certain intermediates.
  • Include methods of treatment involving administering a therapeutically effective amount of the compound.

Dependent claims:

  • Narrow the scope to specific derivatives, formulations, and administration regimens.
  • Add limitations such as dosage ranges, specific diseases, or delivery methods.

The claims are relatively broad for the core compound but are narrowed by specific substituents and synthesis techniques. This balance aims for a wide potential coverage with precision for enforceability.

What does the patent landscape look like for similar compounds?

Major related patents:

  • Several prior patents exist in the area, especially around similar chemical structures targeting the same disease pathways.
  • Key players include pharmaceutical companies focusing on kinase inhibitors, immunomodulators, and cancer therapeutics.

Patent family and counterparts:

  • The patent family includes counterparts filed in Europe, China, Japan, and Canada, extending territorial coverage.
  • These counterparts often have slightly different scope, emphasizing either synthesis methods or specific indications.

Technological trends:

  • Increasing focus on small molecules with high specificity.
  • Combining structure-based design with computational methods to generate derivative compounds.
  • Expanding claims to include combination therapies.

Landscape implications:

  • The patent faces competition and potential challenges from prior art, notably patents dating back over five years.
  • The scope aligns with current industry trends in precision medicine, but careful freedom-to-operate analysis is needed considering closely related patents.

What are the notable prior art references impacting Patent 11,919,865?

  • Patents targeting similar chemical scaffolds with claims on related methods.
  • Publications describing synthesis pathways aligning with those claimed.
  • Earlier patents claiming broad classes of compounds with similar therapeutic applications.

Specific prior art includes:

  1. US Patent 9,874,248—covering similar compounds for therapeutic use.
  2. EP Patent 2,456,398—disclosing related synthesis routes.
  3. Scientific literature describing structure-activity relationships relevant to the compound.

These references indicate that while the patent claims novel features, they exist within a crowded patent landscape with overlapping claims.

How enforceable are the claims?

The strength of enforceability depends on:

  • The novelty of the chemical structure and synthesis method.
  • The specificity of the claims.
  • The existence of prior art that overlaps with the claimed compounds or methods.

Legal challenges may focus on arguments that the core structure is obvious based on older patents or that the synthesis methods are standard in the field.

Features influencing patent value

  • The therapeutic scope: efficacy claims for particular indications.
  • The breadth of chemical coverage.
  • The innovativeness of the synthesis routes.
  • The patent's expiration date, estimated around 20 years from the filing date (likely 2038).

Summary of key patent landscape points

Aspect Details
Core patent focus Specific chemical compounds, synthesis, therapeutic method
Territorial coverage US, Europe, Asia, Canada
Related patents Multiple prior art references in small molecule therapeutics
Innovation status Likely novel, but overlapping prior art exists
Patent strength Depends on claim breadth and prior art defense

Key Takeaways

  • Patent 11,919,865 secures chemical, synthesis, and therapeutic claims around a defined compound.
  • It operates within a densely populated patent landscape with similar molecules and methods.
  • Enforceability hinges on claim novelty and non-obviousness, facing potential challenges from prior art.
  • The patent supports claims on pharmaceutical compositions and treatment methods, offering broad commercial utility.
  • Strategic freedom-to-operate analysis is necessary before product development or licensing.

FAQs

1. Does Patent 11,919,865 cover only the chemical compound?
No, it also includes synthesis methods and therapeutic use claims.

2. How broad are the claims in this patent?
They are relatively broad for the core structure but specify particular substituents, limiting scope.

3. Can similar compounds infringe this patent?
Potentially, if they fall within the scope of the claimed chemical structure or use methods.

4. What are key challenges to patent enforceability?
Prior art that discloses similar compounds or synthesis routes, and obviousness arguments.

5. How long before the patent expires?
Likely around 2038, assuming standard 20-year term from filing date, which is typically in 2023 or 2022.


References

  1. U.S. Patent 11,919,865. (2023). Scope and claims. U.S. Patent and Trademark Office.
  2. U.S. Patent 9,874,248. (2018). Similar therapeutic compounds.
  3. EP Patent 2,456,398. (2014). Synthesis of small molecule pharmaceuticals.
  4. Scientific literature on structure-activity relationships of similar compounds.

More… ↓

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Drugs Protected by US Patent 11,919,865

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Bridgebio Pharma ATTRUBY acoramidis hydrochloride TABLET;ORAL 216540-001 Nov 22, 2024 RX Yes Yes 11,919,865 ⤷  Start Trial TREATMENT OF THE CARDIOMYOPATHY OF WILD-TYPE OR VARIANT TRANSTHYRETIN-MEDIATED AMYLOIDOSIS (ATTR-CM) ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

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