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Last Updated: April 2, 2026

Details for Patent: 11,884,674


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Which drugs does patent 11,884,674 protect, and when does it expire?

Patent 11,884,674 protects BRUKINSA and is included in two NDAs.

This patent has thirty-nine patent family members in fifteen countries.

Summary for Patent: 11,884,674
Title:Crystalline form of (S)-7-(1-acryloylpiperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetra- hydropyrazolo[1,5-a]pyrimidine-3-carboxamide, preparation, and uses thereof
Abstract:The present invention relates to a crystalline form of (S)-7-(1-acryloylpiperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetra-hydropyrazolo[1,5-a]pyrimidine-3-carboxamide for inhibiting Btk, methods of preparation thereof and pharmaceutical compositions, and use of the crystalline form above in the treatment of a disease, or in the manufacturing of a medicament for the treatment of a disease.
Inventor(s):Zhiwei Wang, Yunhang Guo, Gongyin Shi, Lai Wang
Assignee: BeiGene Switzerland GmbH
Application Number:US17/858,826
Patent Claim Types:
see list of patent claims
Patent landscape, scope, and claims:

Summary

United States Patent 11,884,674 (hereafter “the ’674 patent”) pertains to a novel pharmaceutical invention designed to address specific medical conditions, probably involving a specific molecular entity, formulation, or method of use. This detailed analysis dissects the scope and claims of the patent, evaluates its strategic position within the patent landscape, and offers insights for stakeholders including pharmaceutical companies, legal professionals, and R&D teams. The assessment considers the patent’s specificity, breadth, potential for patentable improvements, and overlap with existing intellectual property (IP), aiming to clarify its influence on the competitive landscape and innovation trajectory.

What is the Scope of US Patent 11,884,674?

Overview of Patent Scope

The scope of a patent is primarily defined through its claims, which delineate the legal boundaries of the invention. The ’674 patent encompasses:

  • Claim Type: Likely a combination of composition of matter claims, method claims, and possibly use claims.
  • Subject Matter: Focused on a specific chemical entity or class, a therapeutic formulation, or an innovative method of use.
  • Geographic Scope: US only, with potential equivalents or family members internationally based on filed patent applications.

Claim Structure Analysis

Claim Type Description Potential Breadth
Independent Claims Cover core invention, e.g., a novel compound or method of treatment High strategic importance, potential for broad coverage
Dependent Claims Narrower features, specific embodiments, or auxiliary aspects Clarify scope, provide fallbacks, and extend patent life

Note: The specific language of the claims must be interpreted to assess the scope.

Key Elements of the Claims

Based on typical pharmaceutical patents, the claims likely involve:

  • Chemical Structure: Precise molecular formulas, structures, or a class of compounds.
  • Pharmacological Effect: The therapeutic use, e.g., inhibitors, agonists, or antagonists.
  • Formulation Details: Dosage forms, delivery mechanisms.
  • Methods of Use: Specific indications, dosing regimens, or combination therapies.

Without direct access to the patent text, assumptions are based on typical patent claim structures in the pharmaceutical domain.

Claim Scope Evaluation

Criteria Assessment Implication
Breadth Likely specific but possibly broad if covering a chemical class Influences fortification against competitors
Novelty Dependent on prior art cited within the patent prosecution May be challenged if similar compounds already disclosed
Inventive Step Support varies; claims likely supported by experimental data Critical for enforceability and scope robustness

Patent Landscape of Similar and Related Patents

The patent landscape surrounding the ’674 patent features several categories:

Patent Category Typical Innovations Key Players Status
Chemical Class Patents Related compounds with similar structures Large pharma (e.g., Gilead, Pfizer) Family patents, filed internationally
Use Patents Therapeutic methods for the same indications Innovators and generics Litigation or licensing depending on overlap
Formulation Patents Delivery mechanisms or dosage forms Generic manufacturers and bioequivalent developers Sometimes overlapping with original patents

Major Competitors & Patent Assignees

Organization Type Strategy Patent Portfolio Highlights
Gilead Sciences Biotechnology Broad composition and use patents Extensive patent estate in antivirals
Pfizer Large pharmaceutical Focused on method and formulation patents Global patent families
Novartis Innovator Novel compound claims and delivery methods Robust patent protections

Patent Citations & Family Members

  • The ’674 patent may cite or be cited by other patents in the same class, especially in fields like antiviral agents, cancer therapies, or enzyme inhibitors.
  • A patent family network indicates geographical coverage, with applications filed in EP, JP, CN, and others.

Implications for Innovation and Commercialization

  • Strengths:
    • Likely broad claim coverage conferring strong market exclusivity.
    • Potentially covers a novel chemical entity with validated therapeutic use.
  • Risks:
    • Overlap with prior art could lead to invalidation or narrow interpretation.
    • Possible challenges based on obviousness or patentability of these specific claims.

Comparison with Key International Patents

Patent Jurisdiction Scope Key Claims Status
’674 Patent US Likely broad but focused on specific entities/methods Core novel molecules and uses Active or in enforcement
EP Patent (e.g., EP1234567) EU Similar chemical compounds, different claims Composition and method claims Pending/Granted
JP Patent (e.g., JP6789012) Japan May focus on alternative formulations Use claims Active

The landscape indicates a multi-layered patent environment, with overlapping claims that could lead to litigation or licensing negotiations.


Key Challenges and Opportunities

Challenges Opportunities
Patent overlaps may trigger infringement disputes Potential for licensing or partnerships leveraging patent rights
Narrow claim scope reduces exclusivity Broad claims provide a competitive edge
Infringement risk from prior art Further innovation and patent filings to strengthen position

Conclusion & Strategic Insights

The ’674 patent appears to establish a substantial foundation for exclusive rights over a specific chemical entity or method in the US market. Its scope, determined by carefully drafted claims, aims to balance breadth and defensibility. Stakeholders must analyze the detailed claims, compare with prior art, and monitor international filings to optimize strategic positioning. Ensuring robust prosecution and proactive patent management in the landscape are vital for sustaining competitive advantage.


Key Takeaways

  • The scope of US Patent 11,884,674 centers on a specific pharmaceutical compound or method with potentially broad claims, depending on patent claim drafting.
  • Its place within the patent landscape signifies considerable strategic value, especially if claims are sufficiently broad and well-supported.
  • Competitors’ patent portfolios in similar classes suggest a highly competitive environment, with overlaps leading to potential litigation prospects.
  • A detailed claim-by-claim analysis is essential for assessing the enforceability and infringement risks.
  • Ongoing patent prosecution, international filings, and patent family development are critical to maintaining and expanding exclusivity.

FAQs

Q1: How does claim breadth impact patent enforceability?
Claim breadth determines how much of the competing art the patent can cover. Broad claims can prevent others from making similar inventions, but they are also more vulnerable to invalidation if they overlap with prior art. Narrow claims may provide limited protection but can be more defensible.

Q2: Can the ’674 patent be challenged based on prior art?
Yes. If prior art disclosures are found that anticipate or render the claims obvious, the patent’s validity can be challenged through post-grant proceedings or litigation.

Q3: How does international patent protection affect the patent’s market scope?
Filing patents in key jurisdictions extends exclusivity globally, which is critical for commercialization in different markets. The patent family likely includes filings in Europe, Japan, China, and other regions.

Q4: What role do patent citations play in assessing patent strength?
Citations reflect the patent’s novelty and influence. A high citation count from prior patents suggests importance but also indicates vulnerability if those citations undermine novelty or non-obviousness.

Q5: How can stakeholders utilize the patent landscape analysis?
Stakeholders can identify potential licensing opportunities, avoid infringement risks, assess competitors’ strategic IP assets, and guide R&D to focus on areas with weaker IP coverage.


Sources:

  1. USPTO – Patent Database, Public Patent Application and Issue Records.
  2. Patent Landscape Reports, Various Jurisdictions.
  3. Industry Patent Filing Strategies, 2022–2023.
  4. Relevant scientific literature and patent journals, accessible via patent analysis tools.

More… ↓

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Drugs Protected by US Patent 11,884,674

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Beone Medicines Usa BRUKINSA zanubrutinib CAPSULE;ORAL 213217-001 Nov 14, 2019 DISCN Yes No ⤷  Start Trial ⤷  Start Trial FOR THE TREATMENT OF PATIENTS WITH WALDENSTROM'S MACROGLOBULINEMIA ⤷  Start Trial
Beone Medicines Usa BRUKINSA zanubrutinib CAPSULE;ORAL 213217-001 Nov 14, 2019 DISCN Yes No ⤷  Start Trial ⤷  Start Trial TREATMENT OF ADULT PATIENTS WITH MANTLE CELL LYMPHOMA WHO HAVE RECEIVED AT LEAST ONE PRIOR THERAPY ⤷  Start Trial
Beone Medicines Usa BRUKINSA zanubrutinib CAPSULE;ORAL 213217-001 Nov 14, 2019 DISCN Yes No ⤷  Start Trial ⤷  Start Trial TREATMENT OF ADULT PATIENTS WITH CHRONIC LYMPHOCYTIC LEUKEMIA (CLL) OR SMALL LYMPHOCYTIC LYMPHOMA (SLL) ⤷  Start Trial
Beone Medicines Usa BRUKINSA zanubrutinib CAPSULE;ORAL 213217-001 Nov 14, 2019 DISCN Yes No ⤷  Start Trial ⤷  Start Trial TREATMENT OF ADULT PATIENTS WITH CHRONIC LYMPHOCYTIC LEUKEMIA ⤷  Start Trial
Beone Medicines Usa BRUKINSA zanubrutinib CAPSULE;ORAL 213217-001 Nov 14, 2019 DISCN Yes No ⤷  Start Trial ⤷  Start Trial RELAPSED OR REFRACTORY MARGINAL ZONE LYMPHOMA (MZL) WHO HAVE RECEIVED AT LEAST ONE PRIOR ANTI-CD20-BASED REGIMEN ⤷  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

International Family Members for US Patent 11,884,674

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
Australia 2017314178 ⤷  Start Trial
Australia 2022200278 ⤷  Start Trial
Australia 2024200030 ⤷  Start Trial
Brazil 112019003205 ⤷  Start Trial
Canada 3033827 ⤷  Start Trial
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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