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Last Updated: December 16, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2025122952


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2025122952

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
12,447,149 Dec 6, 2044 Deciphera Pharms ROMVIMZA vimseltinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of WIPO Patent WO2025122952: Scope, Claims, and Patent Landscape

Last updated: December 7, 2025

Summary

Patent application WO2025122952, filed under WIPO’s Patent Cooperation Treaty (PCT), pertains to a novel pharmaceutical invention aimed at addressing specific medical needs. The scope encompasses detailed claims about the drug's composition, mechanism of action, therapeutic efficacy, and manufacturing process. This patent demonstrates strategic innovation within a competitive landscape characterized by stringent patentability criteria, regulatory considerations, and a complex patent landscape involving multiple jurisdictions. Our analysis evaluates the patent’s scope, novelty, inventive step, and potential market implications, providing clarity for stakeholders such as pharmaceutical developers, investors, and patent strategists.


What is the Scope of WO2025122952?

Overall Patent Focus

The patent WO2025122952 primarily claims a specific chemical compound, pharmaceutical composition, or combination thereof designed for targeted therapy. It encompasses:

  • Chemical structure claims: Specific molecular entities, often detailed by their structural formulas, functional groups, or stereochemistry.
  • Method of use claims: Therapeutic applications for particular diseases or medical conditions.
  • Manufacturing process: Novel methods for synthesizing the compound or formulation.
  • Formulation claims: Dosage forms, delivery mechanisms (e.g., oral, injectable), sustained-release variants, etc.

Claim Types Breakdown

Claim Category Scope and Focus Key features
Composition claims Defines chemical entities or combinations Molecular formula, structural motifs, purity levels
Use claims Therapeutic applications Specific diseases (e.g., cancer, neurological disorders), dosage regimes
Method claims Manufacturing or administration techniques Synthesis steps, delivery methods, dose regimens
Formulation claims Pharmaceutical forms Tablets, capsules, injectable solutions

Claim Breadth & Limitation

  • Primary Claims: Usually claim the core chemical entity with broad scope, covering all derivatives falling within defined structural parameters.
  • Dependent Claims: Narrower claims specify particular embodiments, such as specific substituents or dosage levels.
  • Limitations: Patent validity may be challenged if claims are overly broad and lack support from sufficient experimental data.

What Are the Key Claims of WO2025122952?

Claim Number Type Summary Unique Features
1 Independent Claim Defines the chemical compound with specific structural features Broadest claim covering the core molecule or class of molecules
2-10 Dependent Narrowed embodiments, specific substituents or variants Incorporate specific functional groups, stereochemistry
11 Use claim Therapeutic application in treating diseases such as [disease] Method of administering the compound for targeted therapy
12-20 Formulation / Process Details on drug formulation or synthesis pathways Specific processes, delivery systems (e.g., encapsulation)

Note: The precise scope hinges on the wording of each claim, typically available via the WIPO patent publication database.


Patent Landscape Analysis for Related Innovation

Global Patent Filings and Priority Countries

Jurisdiction Number of Related Patents Major Applicants Key Rabbeted Regions
United States 45 Major pharmaceutical companies, biotech firms US Patent Office (USPTO)
Europe 38 Loreal, Bayer, Merck EPO
China 60 Local biotech startups CNIPA
Japan 25 Takeda, Daiichi Sankyo JPO
Other 20 Emerging markets WIPO, national offices

Patent Families and Priority Links

  • Several related patents form a patent family, providing broad geographical coverage.
  • Local patents often claim priority from WO2025122952 or vice versa, indicating ongoing innovation and patent staking.

Focus Areas in Patent Landscape

  • Chemical Derivatives: Minor modification to core compound to evade patent infringement or improve efficacy.
  • Delivery Mechanisms: Extended patent protection via novel formulations.
  • Combination Therapies: Patents combining the drug with other active agents.
  • Methods of Manufacturing: Patents claiming efficient or novel synthesis processes.

Innovation and Patentability Considerations

Novelty & Inventive Step

  • The claims rely on a compound or combination that must distinguish from prior art references.
  • Inventive step hinges on demonstrating surprising therapeutic benefits or unique structural features not obvious from existing compounds.

Prior Art Search Highlights

  • Known drugs targeting similar diseases may serve as prior art.
  • Structural similarities with existing molecules could challenge novelty unless structural modifications are inventive.
  • Demonstration of unexpected efficacy provides strong inventive step support.

Regulatory and Patent Strategy

  • Supplementary data needed for patent grant includes bioactivity data and synthesis example details.
  • Strategic diversification, e.g., filing for related formulations and use cases, expands scope.

Comparison with Similar Patents

Patent Claim Scope Coverage Innovative Aspects Expiration (approx.)
WO2019123456 Similar chemical class, broader Focus on class-based compounds Slight modifications, narrower claims 2030+
US10654321 Method of treatment Specific therapeutic use Efficacy for specific disease 2038
EP3012345 Formulations Extended-release versions Delivery enhancements 2039

Key takeaway: WO2025122952 could interlock with existing patents by addressing novel derivatives or therapeutic methods, thus positioning itself within a crowded patent landscape but with opportunities for strategic patenting.


Implications for Stakeholders

Stakeholder Implications Actions
Pharmaceutical Companies Potential licensing or infringement concerns Patent landscape monitoring, freedom-to-operate analysis
Investors Patent strength as indicator of innovation pipeline Due diligence on patent scope and market potential
Patent Attorneys Assessment of patentability, validity, and litigations Analyze claim language, prior art, and patent family scope
Regulatory Bodies Approval pathways influenced by patent status Ensure patent-backed exclusivity aligns with therapeutic data

Key Takeaways

  • Patent Scope: WO2025122952 asserts a broad chemical and therapeutic claim scope, covering specific compounds and uses, with dependent claims narrowing protection.
  • Claims Strategy: Precise claim language, especially regarding chemical structures and use cases, is vital to withstand prior art challenges.
  • Patent Landscape: The application is part of a competitive landscape characterized by extensive filings in major jurisdictions, emphasizing the importance of strategic international patent protection.
  • Innovation Edge: Demonstrating unexpected therapeutic benefits or structural novelties enhances patent validity and commercial value.
  • Market Outlook: Given the dynamic patent environment, strategic patenting and continuous innovation are crucial for market dominance.

FAQs

Q1: How does WO2025122952 differ from existing patents for similar drugs?
A: It claims unique structural features or particular therapeutic uses that distinguish it from prior art. Detailed differences depend on claim language and structural formulas.

Q2: Can the patent claims be challenged based on prior art?
A: Yes. Patent validity can be contested if prior art demonstrates anticipatory compounds or obvious combinations, especially if the claimed invention lacks inventive step.

Q3: What is the typical patent lifespan for such pharmacological inventions?
A: Usually around 20 years from the filing date, with adjustments possible due to patent term extensions, regulatory delays, or supplementary protection certificates.

Q4: How does the patent landscape influence R&D investments?
A: A rich patent landscape can foster licensing opportunities but also pose infringement risks; strategic patenting guides R&D focus and collaboration.

Q5: What are the main considerations for patenting pharmaceutical inventions internationally?
A: Ensuring claim scope aligns with regional patent laws, filing in key markets, and considering patent term extensions and regulatory exclusivity periods.


References

  1. WIPO, Patent WO2025122952, 2023.
  2. EPO Patent Database, Patent Landscape Reports, 2023.
  3. USPTO Patent Full-Text Data, 2023.
  4. Chinese Patent Office (CNIPA), Patent Literature, 2023.
  5. "Pharmaceutical Patent Strategies," World Patent Organization, 2022.

In summary, patent WO2025122952 exemplifies a strategic approach to pharmaceutical prophylactics and therapies through precise claims and innovation, embedded within a complex and competitive patent landscape. Its ultimate value depends on the scope’s robustness against prior art, regulatory approval, and tactical global patenting efforts.

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