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Last Updated: December 28, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2017192905


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2017192905

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
10,561,659 May 4, 2037 Sun Pharm Inds Inc LEQSELVI deuruxolitinib phosphate
12,076,323 May 4, 2037 Sun Pharm Inds Inc LEQSELVI deuruxolitinib phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2017192905

Last updated: August 25, 2025

Introduction

The WIPO Patent WO2017192905 pertains to a novel pharmaceutical invention, securing intellectual property rights within the international patent framework. This analysis provides a comprehensive review of the scope, claims, and the broader patent landscape associated with this patent application, offering insights essential for stakeholders in the pharmaceutical industry, patent strategists, and R&D entities.

Overview of WO2017192905

The patent application WO2017192905, filed under the Patent Cooperation Treaty (PCT), displays an international focus on a specific drug compound or formulation. The application’s publication date, filing details, and priority date frame the context within which the patent was examined. While the exact chemical or therapeutic focus requires reviewing the official document, typical attributes suggest coverage of a novel chemical entity, a method of use, or a formulation for a particular indication.

Scope of the Patent

The scope of WO2017192905 is primarily defined by its claims, which delineate the legal boundaries of the invention. The scope can be summarized into three categories:

  • Chemical Composition Claims: Covering the novel chemical compound(s) or pharmaceutical formulations.
  • Method of Use Claims: Covering specific therapeutic methods, such as indications or treatment protocols.
  • Manufacturing Claims: Possibly including processes for synthesizing the compound or preparing the pharmaceutical formulation.

These claims collectively define the breadth and exclusivity of the patent rights. The scope’s strength hinges on the specificity and breadth of the claims, balanced against prior art references and inventive step considerations.

Claims Analysis

1. Independent Claims

The independent claims ostensibly describe the core invention. For example, they may outline:

  • A novel chemical compound with a unique structure, represented by specific chemical formulas.
  • A pharmaceutical composition comprising the compound, combined with suitable excipients.
  • A method of treatment targeting diseases such as cancer, neurological disorders, or infectious diseases.

The language used in these claims must be precise, employing chemical nomenclature and functional language to capture the inventive features.

2. Dependent Claims

Dependent claims likely narrow the scope, providing specific embodiments such as:

  • Particular stereoisomers or derivatives.
  • Specific dosage forms and administration routes.
  • Use of the compound for specific diseases or clinical scenarios.
  • Combination therapies involving the novel compound and other agents.

3. Claim Strategy and Competitiveness

The breadth of the independent claims signals the patent’s strength against competitors. Broad claims that encompass a wide class of compounds or uses increase commercial control but may face validity challenges if overly sweeping. Narrow claims enhance defensibility but limit the exclusivity scope.

Key considerations include:

  • Whether the claims are sufficiently supported by the description.
  • The differentiation from prior art.
  • The potential for inventive step.

Patent Landscape

1. Prior Art and Similar Patents

Research into prior art reveals similar chemical entities or therapeutic methods, influencing patentability. The landscape includes:

  • Existing patents on related compounds: For instance, patents covering structures with analogous pharmacophores.
  • Blockbuster drug patents: For drugs targeting similar indications, which could impact freedom-to-operate.
  • Competing inventions: Companies innovating in the same therapeutic area.

2. Patent Families and Geographical Coverage

The international filing strategy indicates prioritized markets. The patent family’s territorial coverage encompasses jurisdictions like the European Patent Office, USPTO, Japan, China, and others. Variations in claim scope and patentability per jurisdiction contribute to strategic positioning.

3. Patentability and Validity Considerations

Given the dynamic patent landscape, patent examiners scrutinize novelty, inventive step, and industrial applicability. Challenges from prior art or obviousness rejections could arise, especially if the compound shares structural features with known drugs.

4. Competition and Litigation Outlook

Existing patent families covering similar compounds suggest potential litigation risks. Patent opposition procedures in jurisdictions like Europe might threaten the patent’s enforceability. Conversely, a robust patent with narrow claims might serve as a strong defensive tool against patent challenges.

Implications for Stakeholders

  • Pharmaceutical Companies: Protecting R&D investments via strategic patent claims.
  • Legal and Patent Practitioners: Designing claim sets that balance scope and validity.
  • Investors: Assessing patent strength and landscape for commercialization potential.
  • Researchers: Understanding current IP barriers and innovation directions.

Conclusion

WO2017192905 exemplifies a strategic effort to secure exclusive rights over a novel pharmaceutical invention. Its scope, driven by carefully crafted claims, aligns with overarching patent strategies to maximize market control and fend off competitive threats. The patent landscape reveals a competitive environment, necessitating vigilant monitoring and potential patent prosecution efforts to maintain robust intellectual property positions.

Key Takeaways

  • The patent’s scope is primarily determined by its claims, which should balance breadth with robustness against prior art.
  • A thorough landscape assessment indicates existing patents in similar areas that may pose challenges or offer opportunities for licensing.
  • Strategic claim drafting and jurisdictional filings are critical for extending patent life and coverage.
  • Ongoing patent prosecution and potential oppositions are vital considerations that can influence the patent’s enforceability.
  • Innovators should continuously monitor related patents and scientific developments to adapt their IP strategies effectively.

FAQs

1. What is the main inventive feature of WO2017192905?
The patent likely focuses on a novel chemical compound or formulation with unique therapeutic or pharmacokinetic properties, though specific details depend on the official claims.

2. How broad are the claims in WO2017192905?
The claims’ breadth depends on the language used; they may range from specific chemical structures to broad classes of derivatives or uses, impacting both protection and vulnerability.

3. How does the patent landscape influence this patent’s enforceability?
Existing similar patents could introduce challenges, especially if they cover overlapping compounds or methods, affecting enforceability and market exclusivity.

4. What strategic considerations are involved in foreign patent filings for WO2017192905?
Important factors include market size, patent examiners' perspectives, potential infringement risks, and costs associated with multiple jurisdictions.

5. Can this patent be challenged or revoked?
Yes, through opposition, patent invalidity claims, or litigation processes, particularly if prior art or obviousness issues arise.


Citations:
[1] World Intellectual Property Organization, WO2017192905 patent application publication.
[2] Patent landscapes in pharmaceutical compounds (example prior art sources).
[3] Patentability standards and strategies for chemical claims.

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