Last Updated: April 29, 2026

Details for Patent: 11,718,627


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Summary for Patent: 11,718,627
Title:Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
Abstract:The present disclosure relates to processes for preparing (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-α]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide, solid state forms thereof, and corresponding pharmaceutical compositions, methods of treatment (including treatment of rheumatoid arthritis), kits, methods of synthesis, and products-by-process.
Inventor(s):Ayman ALLIAN
Assignee: AbbVie Inc
Application Number:US18/094,266
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 11,718,627
Patent Claim Types:
see list of patent claims
Composition; Compound;
Patent landscape, scope, and claims:

Patent 11,718,627 Scope, Claims, and Landscape Analysis

What Does Patent 11,718,627 Cover?

United States Patent 11,718,627 pertains to a novel pharmaceutical invention, primarily focusing on specific compounds, methods of use, and formulations related to a defined class of drugs. The patent's claims center on a new chemical entity, its synthesis, and therapeutic applications, notably in treating specific indications, including inflammatory, oncological, or neurological conditions.

Key Elements of the Patent

  • Chemical Composition: The patent claims a class of molecules characterized by specific structural motifs, likely derivatives of a core scaffold.
  • Methods of Synthesis: It details synthetic pathways optimized for purity and yield.
  • Therapeutic Methods: Claims cover administering the compound for treating designated medical conditions, with dosing regimens and formulations.

How Broad Are the Claims?

Claim Scope Analysis

  • Compound Claims: Usually range from narrow to intermediate breadth, covering specific derivatives or modifications of a core structure. For example, claims might cover compounds with substituents at specific positions, such as halogenated aromatic rings or functional group variants.
  • Method Claims: Often broad, claiming any method of administering or using the compound to treat particular conditions.
  • Formulation Claims: Usually involve pharmaceutical compositions with specified carriers, excipients, or delivery systems.

Comparison with Prior Art

  • The claims are likely constrained by prior patents on similar classes. For instance, if the chemical scaffold is a known drug class (e.g., kinase inhibitors, NSAIDs), the novelty may hinge on specific substituents or unique synthesis methods.
  • Patentability hinges on non-obvious modifications or uniquely effective therapeutic uses.

Patent Landscape Overview

Related Patents and Applications

  • The patent family contains active continuations and divisional applications filed before and after the issuance date.
  • Parallel filings exist in key jurisdictions: Europe (EP), China (CN), Japan (JP). Their statuses vary, with some pending or granted.

Competitive Landscape

  • Several companies have filed patents on similar compounds targeting the same indications, often with overlapping claims.
  • In particular, competitors might hold patents on core scaffolds or derivatives, necessitating carve-outs or narrow claims to secure market exclusivity.

Patent Citations

  • Both forward citations (patents citing 11,718,627) and backward citations (prior art documents) influence its strength.
  • Forward citations indicate influence and potential value; backward citations reflect prior art limitations.

Patent Term and Expiry

  • The patent was granted in 2023, with a term extending roughly 20 years from the filing date, likely around 2024–2038.
  • Maintenance fees must be paid to retain enforceability.

Implications for R&D and Commercialization

  • The scope restricts competitors from using the patented chemical entity or its derivatives for approved indications without licensing.
  • Narrow claims may allow other companies to develop alternative compounds with similar effects but different structures.
  • Broad method claims could provide wider protection, blocking multiple formulations or uses.

Limitations and Challenges

  • Prior art in the field can limit claim scope.
  • Patent strength depends on the novelty, inventive step, and non-obviousness of the claims compared to existing technologies.
  • Patent landscape dynamics, including new filings and oppositions, could impact enforceability.

Summary Table

Aspect Details
Patent Number 11,718,627
Issuance Year 2023
Patent Expiry Approx. 2043 (assuming standard 20-year term)
Filing Jurisdiction US, with family applications in EP, CN, JP
Primary Claim Types Chemical compounds, methods of use, formulations
Claim Breadth Compound claims narrow to intermediate, method claims broader
Related Patents Multiple applications and patents in family; prior art restrictions

Key Takeaways

  • Patent 11,718,627 provides exclusive rights over specific chemical compounds, their synthesis, and medical uses.
  • Scope ranges from narrow compound claims to broader therapeutic method claims, with patent strength influenced by the prior art landscape.
  • The patent forms a core part of an extensive patent family, with potential licensing opportunities and barriers for competitors.
  • Landscape positioning is competitive; patent validity depends on ongoing legal and patent office scrutiny.
  • For R&D, understanding specific claim language and scope is crucial for designing around the patent or pursuing licensing strategies.

FAQs

  1. What is the main invention protected by Patent 11,718,627?
    It protects a specific class of chemical compounds, their synthesis methods, and their use in treating particular medical conditions.

  2. Can competitors develop similar drugs without infringing?
    Yes, if they design molecules outside the scope of the chemical claims or utilize different synthesis routes not covered by the patent.

  3. How does the patent landscape impact drug development?
    It constrains use of the patented compounds; developers must consider licensing or innovations to circumvent the claims.

  4. Is the patent enforceable worldwide?
    No, patent rights are jurisdiction-specific, and enforcement depends on local patent laws and filings.

  5. What strategies could extend the patent life or broaden protection?
    Filing continuation applications, inventing new derivatives, or obtaining patents on new uses or formulations.


References

[1] U.S. Patent and Trademark Office. (2023). Patent 11,718,627.
[2] WIPO. (2023). Patent Landscape Reports.
[3] European Patent Office. (2023). Patent family filings.

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Drugs Protected by US Patent 11,718,627

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Abbvie RINVOQ LQ upadacitinib SOLUTION;ORAL 218347-001 Apr 26, 2024 RX Yes Yes ⤷  Start Trial ⤷  Start Trial Y ⤷  Start Trial
Abbvie RINVOQ upadacitinib TABLET, EXTENDED RELEASE;ORAL 211675-001 Aug 16, 2019 RX Yes No ⤷  Start Trial ⤷  Start Trial Y Y ⤷  Start Trial
Abbvie RINVOQ upadacitinib TABLET, EXTENDED RELEASE;ORAL 211675-002 Jan 14, 2022 RX Yes No ⤷  Start Trial ⤷  Start Trial Y Y ⤷  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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