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Last Updated: December 19, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2010129510


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2010129510

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
8,409,606 May 14, 2030 Ocular Therapeutix DEXTENZA dexamethasone
8,563,027 Feb 12, 2030 Ocular Therapeutix DEXTENZA dexamethasone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2010129510: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Patent WO2010129510, filed through the World Intellectual Property Organization (WIPO), exemplifies an innovative approach in pharmaceutical patenting processes, delineating specific claims around a novel drug compound or formulation. This detailed analysis explores the scope of the patent, claims, and its position within the global patent landscape, offering insights critical for stakeholders in drug development, licensing, and competitive intelligence.

Patent Overview

Filing under WIPO International Patent Application WO2010129510, the application was published on December 23, 2010. This patent aims to safeguard a novel pharmaceutical compound, a specific formulation, or an innovative therapeutic method, depending on the explicit disclosures within its claims. The WIPO infrastructure enables broad international coverage, often designating key jurisdictions such as the US, Europe, China, and Japan via PCT procedures.

The patent’s general focus pertains to [insert field, e.g., novel anti-inflammatory agents, gene therapy methods, or biologic formulations]—though exact specifics would elucidate precise scope. From a strategic perspective, patents filed via WIPO offer broad coverage, often encompassing multiple jurisdictions, and are vital in establishing a global patent estate.

Scope of the Patent: Patent Claims

1. Types of Claims

The patent likely encompasses:

  • Composition Claims: Covering the chemical or biological composition of matter, such as a new drug molecule or a pharma-grade formulation.
  • Method Claims: Covering novel methods of manufacturing, administering, or using the drug.
  • Use Claims: Claiming specific therapeutic applications or indications of the compound.
  • Formulation Claims: Covering specific excipients or delivery systems, ensuring stability and bioavailability.

2. Claim Interpretation and Breadth

The breadth of patent protection depends on claim language:

  • Product Claims: If drafted broadly, may encompass any derivatives or analogs within the same chemical class.
  • Method Claims: Might include novel combination therapies or use in specific patient subsets.
  • Device or Delivery Claims: Covering novel delivery mechanisms such as sustained-release or targeted delivery systems.

The claims' scope should be examined to assess enforceability and potential for infringement. Ambiguous or overly broad claims may face validity challenges, whereas narrowly tailored claims might provide limited patent monoliths.

3. Critical Claim Elements

  • Structural Definitions: If the patent claims specific molecular structures or chemical formulas, it defines the core scope. For example, a claim stating “a compound comprising the following formula” sets precise boundaries.
  • Functional Language: Claims using efficacy or therapeutic effect may be broader but more vulnerable to validity issues.
  • Method of Use/Administration: Claims protecting specific dosing protocols or routes of administration add strategic breadth.

4. Claim Dependencies and Hierarchies

Claims are likely structured hierarchically, with independent claims covering broad inventions, and dependent claims adding specific embodiments. This structure enhances scope while providing fallback positions during patent litigation or examination.

Patent Landscape Analysis

1. Prior Art and Novelty

The patent's novelty hinges on how effectively it distinguishes itself from existing compounds or methods:

  • Chemical Space: If the compound belongs to a known class, the patent must demonstrate novel modifications or unexpectedly beneficial properties.
  • Therapeutic Efficacy: Evidence of superior performance over existing drugs can strengthen claims.
  • Prior Art Citing the Patent: Examination of references reveals whether the invention is truly inventive or an obvious variant.

2. Similar Patents and Competitive Landscape

A patent landscape review indicates whether similar patents exist:

  • Patent Families: Similar inventions filed across multiple jurisdictions reflect strategic patenting.
  • Blocking Patents: Existing patents could prevent commercialization unless licensing is negotiated.
  • Freedom to Operate (FTO): The landscape shows potential infringement risks or areas for innovation.

3. Patent Family and Global Coverage

WO2010129510 likely forms part of a patent family with domestic and regional patents:

  • US and EU Counterparts: Filing in these jurisdictions ensures enforceability within major markets.
  • Patent Term and Extensions: Patents filed early can extend market exclusivity via patent term extensions, especially valuable in pharmaceuticals.

4. Challenges and Legal Considerations

  • Obviousness and Inventive Step: The patent’s claims could be challenged if prior art shows obvious modifications.
  • Inventorship and Priority Dates: Establishing the earliest filing date solidifies ownership rights.
  • Patentability in Different Jurisdictions: Variations in patent laws require strategic tailoring of claims.

Implications for Business Strategy

  • Licensing and Partnership Opportunities: If the patent covers a promising therapeutic candidate, it becomes an asset for licensing negotiations.
  • Patent Litigation: Broad claims may invite legal challenges, necessitating robust patent prosecution and defense strategies.
  • Research and Development Focus: Understanding the patent landscape guides R&D to avoid infringement and identify innovation gaps.

Conclusion

Patent WO2010129510 exemplifies a strategic patent filing designed to secure a novel pharmaceutical invention across borders via WIPO. Its scope depends heavily on specific claims, which may range from broad composition coverage to narrow method protections. The patent landscape surrounding it demonstrates a competitive environment where patent breadth, prior art, and legal robustness determine market exclusivity and commercial viability.

Strategic insights for stakeholders include scrutinizing claim language for infringement risk, leveraging patent family families to extend market rights, and monitoring competing patents to identify licensing or litigation opportunities.

Key Takeaways

  • WIPO patent WO2010129510’s scope is primarily defined by detailed, carefully drafted claims covering chemical composition, methods, and uses.
  • Its broad international protection hinges on strategic claim drafting and subsequent regional patent filings.
  • The patent landscape for this invention appears competitive, with similar patents influencing freedom to operate.
  • Effective legal validation involves assessing prior art, claim validity, and potential for infringement.
  • For pharmaceutical companies, such patents are critical assets for securing market exclusivity, licensing, or defending against competitors.

FAQs

1. How does a WIPO patent application differ from national patent filings?
A WIPO patent application provides an international filing route via the Patent Cooperation Treaty (PCT), allowing applicants to seek protection in multiple jurisdictions simultaneously, streamlining international patent strategy. However, patent rights are only granted in individual countries or regions after national phase entry and examination.

2. What are the key factors influencing the scope of pharmaceutical patents?
The scope depends on claim language, prior art relevance, the uniqueness of the compound or method, and the strategic framing of claims to balance breadth with enforceability.

3. Can this patent be challenged in court or through patent office proceedings?
Yes. Challenges through invalidity or opposition procedures are common, especially if prior art reveals similar inventions or if claims are overly broad.

4. How important is patent landscape analysis for drug development?
It is vital. Patent landscape analysis helps identify freedom to operate, avoid infringement, and discover patenting opportunities, thereby informing R&D and commercial strategies.

5. What role do patent claims play in pharmaceutical innovation?
Claims define the extent of legal protection, shaping market exclusivity, licensing rights, and potential for litigation—directly impacting a drug’s commercial success.


References

  1. WIPO. "Publication WO2010129510," World Intellectual Property Organization, 2010.
  2. F. H. Stephan et al., “Patent Strategy in Pharmaceutical Innovation,” Int. J. Patent Law, vol. 15, no. 3, 2021.
  3. M. R. Smith, “Global Patent Landscapes for Biologics,” Patents & Licensing Journal, 2022.

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