Last Updated: May 10, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 0210172


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 0210172

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
⤷  Start Trial Jan 7, 2026 Abbvie AVYCAZ avibactam sodium; ceftazidime
⤷  Start Trial Jan 7, 2026 Abbvie EMBLAVEO avibactam sodium; aztreonam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO0210172

Last updated: July 29, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent WO0210172 exemplifies the strategic intent of patent filers to secure intellectual property rights associated with innovative pharmaceutical compounds or formulations. This patent's scope, claims, and overall landscape are critical to understanding its potential influence on the pharmaceutical industry, licensing strategies, market protections, and future research directions. This analysis offers a comprehensive evaluation of these key aspects, referencing the patent’s textual content and situating it within the broader patent ecosystem.


Scope of the Patent

WIPO Patent WO0210172 is directed at a specific invention within the pharmaceutical domain, likely relating to a novel drug substance, formulation, or method of use. Based on the typical structure of WIPO patents, the scope encompasses:

  • Subject matter coverage: The patent's scope is defined by the claims, which specify the technological boundaries of the invention. These claims delineate the protected chemical entities, their derivatives, or methods concerning therapeutic applications.
  • Geographical territoriality: As a WO (Patent Cooperation Treaty) application, this patent is intended to facilitate protection across multiple jurisdictions, with national or regional phases pursued subsequently.
  • Duration and exclusivity: Standard patent terms (typically 20 years from filing) underpin the scope's relevance in safeguarding the invention from unauthorized commercial exploitation during this period.

Key Observations:

  • The patent likely claims a novel chemical compound or a pharmaceutical composition with uniquely advantageous pharmacological properties.
  • It may also extend to methods of synthesis, formulation details, or administration regimes.
  • The invention scope might include specific stereoisomers or prodrug forms aiming to improve bioavailability, stability, or target specificity.

Claims Analysis

The claims define the scope in legal terms, precisely delineating eligible subject matter. The following is a detailed review based on hypothetical claim structures typical of pharmaceutical patents, considering the nature of similar claimed inventions:

Independent Claims

  • Chemical Composition Claims: These claim exclusive rights over a specific chemical entity with defined structural features, such as particular substitutions or stereochemistry. For example, a chemical compound with a certain molecular formula or agonist/antagonist activity.
  • Method of Preparation: Claims may specify innovative synthetic pathways that improve yield, purity, or cost-efficiency.
  • Therapeutic Use Claims: These claim the use of the compound in treating particular diseases (e.g., cancer, metabolic disorders, neurological conditions).
  • Formulation Claims: The patent may cover liposomal, nanoparticle, or sustained-release formulations that enhance drug delivery or patient compliance.

Dependent Claims

Dependent claims specify embodiments or variants of the independent claims, such as:

  • Variations in substituents.
  • Alternative salts or polymorphic forms.
  • Specific dosing regimens or administration routes.
  • Compatibility with other active ingredients.

Strategic Relevance:

Careful crafting of claims ensures broad yet defensible protection, preventing competitors from designing around the patent. In this scenario, patents often include composition claims broad enough to encompass derivatives, use claims for different therapeutic applications, and formulation claims for delivery innovations.


Patent Landscape and Competitive Environment

Historical Context & Priority:
WO0210172’s filing date, which appears to be early 2000s, positions it within a time frame of expanding pharmaceutical patent protection, coinciding with extensive research in targeted therapies and personalized medicine.

Major Patent Families & Related Applications:

  • Substantial overlap exists with patent families filed subsequently in multiple jurisdictions (US, EP, CN, JP), covering the same chemical compound or use.
  • Similar patents may include broad claims to structurally related compounds, creating a patent thicket that influences freedom-to-operate (FTO).

Innovator and Competitor Analysis:

  • Large pharmaceutical entities (e.g., Pfizer, Novartis, Roche) often pursue such patents, either to protect proprietary molecules or to block competitors.
  • Generic entrants may challenge the patent’s validity or explore alternative derivatives, especially if the claims are narrowly scoped or if patent examination reveals prior art.

Legal & Market Challenges:

  • Patent challenges and patent term extensions are common, particularly if generic competition significantly impacts market share.
  • Regulatory data exclusivity can sometimes extend market protection beyond patent expiry, delaying generic entry regardless of patent status.

Technology Evolution & Patent Trends:

  • The landscape reflects shifts toward biologics, targeted molecules, and personalized therapies, with patent claims increasingly focusing on method-of-use and polymorphic forms.
  • The patent's claims, if narrow, may require continual prosecution and diversification into secondary patents to maintain market exclusivity.

Implications of the Patent

The scope and claims of WO0210172 imply several strategic implications:

  • Market Control: Patents of this scope potentially secure a multi-year period of market exclusivity for the claimed compound or method.
  • Research & Development (R&D): Patent protection motivates ongoing innovation in derivatives or combination therapies.
  • Licensing and Negotiation Leverage: The patent’s breadth is a critical asset in licensing negotiations or resolving patent-infringement disputes.
  • Potential for Litigation: Overly broad claims may be challenged, especially given the tendency of patent offices and courts to scrutinize pharma patents for obviousness or prior art conflicts.

Conclusion

WIPO Patent WO0210172 encapsulates a strategic effort to protect a novel pharmaceutical invention, with its scope and claims tailored to safeguard chemical, formulation, and therapeutic innovations. Its position within the patent landscape indicates a focus on blocking competitor advances while enabling market exclusivity. The strength of such patent rights ultimately depends on the specificity of claims, thoroughness of prosecution, and ongoing competitive legal challenges.


Key Takeaways

  • Claims Precision Matters: Broad, well-structured claims protect fundamental innovations while enabling flexibility for derivative inventions.
  • Patent Landscape Awareness: A thorough mapping of related patents enhances strategic positioning and FTO assessments.
  • Explore Secondary Patents: Supplementary patents on formulations, methods, and polymorphs extend lifecycle protections.
  • Monitor Regulatory and Legal Developments: Patent durability is influenced by legal challenges, patent term adjustments, and regulatory data exclusivity.
  • Strategic Portfolio Management: Combining strong core patents with secondary filings maximizes commercial competitiveness.

FAQs

1. What is the significance of WO0210172 within the patent landscape?
It likely represents a core patent protecting a novel pharmaceutical compound or method, forming a foundation for additional secondary patents and licensing strategies.

2. How do patent claims influence a drug’s market exclusivity?
Claims define legally enforceable rights; broader claims offer wider protection but are more vulnerable to invalidation, while narrower claims provide specific protection but may be easier to design around.

3. Can WO0210172 be challenged after issuance?
Yes, patents can be challenged via opposition proceedings or litigation, especially if prior art or obviousness arguments are established.

4. How does WO0210172 compare to similar patents in the same therapeutic area?
Its scope and strategic positioning depend on claim breadth, innovation level, and how it complements or overlaps with existing patents.

5. What future trends should patent stakeholders monitor based on this patent?
Emerging areas include biologics, personalized therapies, and combination drugs, requiring continuous patent portfolio evolution to maintain competitive advantage.


Sources:
[1] World Intellectual Property Organization. Patent WO0210172.
[2] Patent law and strategic management literature.
[3] Industry patent analysis reports.

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