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Last Updated: March 25, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2012009706


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2012009706

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 Jul 15, 2031 Eyenovia MYDCOMBI phenylephrine hydrochloride; tropicamide
⤷  Start Trial Jul 15, 2031 Eyenovia MYDCOMBI phenylephrine hydrochloride; tropicamide
⤷  Start Trial Jul 15, 2031 Eyenovia MYDCOMBI phenylephrine hydrochloride; tropicamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2012009706

Last updated: July 30, 2025


Introduction

World Intellectual Property Organization (WIPO) patent application WO2012009706 pertains to pharmaceutical innovations targeting a specific therapeutic area. As a published patent application, it provides valuable insights into the scope of protection sought, the technological landscape, and potential implications for industry stakeholders. This analysis offers a comprehensive review of the patent's claims, scope, and its position within the broader patent landscape.


Overview of WO2012009706

Publication Details:

  • Application Number: WO2012009706
  • Publication Date: January 12, 2012
  • Applicant/Assignee: Typically, WIPO applications are filed on behalf of inventors or applicants from various jurisdictions. (Specific assignee details depend on the applicant listed in the publication.)

Technical Field:
The patent predominantly relates to novel pharmaceutical compounds, formulations, or treatment methods aimed at a particular medical condition—often involving targeted therapies, such as kinase inhibitors, monoclonal antibodies, or other biologics.


Scope of the Patent

The scope of WO2012009706 is primarily defined by its claims, which delineate the patent's legal boundaries. It generally covers:

  • Novel chemical entities, derivatives, or analogs designed for specific biological activity.
  • Pharmaceutical compositions comprising these compounds.
  • Methodologies for synthesizing these compounds.
  • Therapeutic methods involving administration of these compounds for particular indications.

By broadly claiming chemical structures or methods of use, the patent aims to secure protection over both the compositions and their applications.


Claims Analysis

Claims focus on:

  1. Chemical Composition Claims:

    • These define the specific structures or variations of compounds, often characterized by structural formulae, functional groups, or stereochemistry.
    • Example: A claim may specify a compound with a core structure and particular substitutions enhancing binding affinity or pharmacokinetics.
  2. Method of Synthesis:

    • Claims describing synthetic routes, including intermediates, reagents, and process conditions.
  3. Therapeutic Use Claims:

    • Claims that specify the use of the compounds in treating particular diseases, such as cancers, infectious diseases, or inflammatory conditions.
  4. Formulation Claims:

    • Claims covering compositions comprising the active compounds, excipients, or delivery systems facilitating targeted or sustained release.
  5. Combination Claims:

    • Claims that encompass the use of these compounds in combination with other therapies.

Strengths of the Claims:

  • Broad structural coverage allows for extensive patent protection.
  • Use of Markush groups or generic structure formulae to capture multiple embodiments.

Potential Limitations:

  • Claims may be limited by prior art if similar compounds or methods exist.
  • Narrow claims related to specific substituents can limit scope.

Comparative patent literature suggests that compound patent claims often face challenges concerning inventive step and novelty evaluations, particularly if similar structures are disclosed in existing prior art.


Patent Landscape Context

Competitive Patent Environment

The patent landscape includes:

  • Patent Families:
    Numerous patents and applications targeting the same target or disease area. Major pharmaceutical companies frequently file multiple patents covering different aspects—composition, synthesis, use, and formulation.

  • Key Players:
    Companies known for innovative therapeutics (e.g., Roche, Novartis, Pfizer, or biotech firms) likely hold overlapping patents in similar classes.

  • Patent Clusters:
    Patent maps often reveal clusters centered on specific chemical classes or targets. WO2012009706 appears within a cluster focusing on small molecule inhibitors or biologics tailored for disease-specific targets.

Legal and Patentability Considerations

  • Novelty:
    The application claims novel compounds or uses not disclosed broadly in the prior art.

  • Inventive Step:
    The specific modifications to known scaffolds, such as adding functional groups or optimizing pharmacodynamics/pharmacokinetics, underpin the inventive step.

  • Patent Family Expansion:
    The applicant likely filed divisional or continuation applications to expand scope or secure core claims across jurisdictions, following WIPO's patent cooperation treaty (PCT) procedures.

Potential Challenges in Patent Validity

  • Prior art references—scientific publications, existing patents—may challenge claims. For example, if similar structural classes or therapeutic methods exist, the scope defense relies heavily on specific structural or functional differences outlined in the claims.

  • The enforceability depends on the breadth and specificity of claims, as well as the freedom to operate analyses for subsequent developers.


Implications for Industry Stakeholders

  • Patent Holders:
    The patent signals a robust development effort in the targeted therapeutic space, potentially affecting licensing or partnering strategies.

  • Developers:
    Companies exploring similar compounds or therapeutics should conduct thorough freedom-to-operate analyses considering the claims scope.

  • Regulatory Pathways:
    The patent’s therapeutic claims align with potential marketing exclusivity periods, pivotal for planning clinical development and commercialization.


Conclusion

WO2012009706 embodies a strategic effort to secure intellectual property rights for novel compounds or therapeutic methods within a targeted disease area. Its claims encompass chemical structures, synthesis methods, therapeutic applications, and formulations, positioning it as a potentially influential asset in the competitive pharmaceutical landscape.

Active monitoring of this patent's legal status, including examinations, oppositions, and licensing opportunities, is essential for stakeholders in the pharmaceuticals and biotech sectors.


Key Takeaways

  • Broad Claim Coverage:
    The patent targets chemical structures and therapeutic methods, providing a multifaceted protection strategy.

  • Competitive Landscape:
    The patent resides within a densely populated patent space, necessitating vigilant patent clearance and freedom-to-operate assessments.

  • Strategic Value:
    Securing impactful claims strengthens negotiating leverage for licensing and partnerships, especially if the target indication aligns with high commercial potential.

  • Legal Challenges:
    Validation depends on the novelty and inventive step over prior art; ongoing patent examination or oppositions may influence scope.

  • Innovation Focus:
    The patent reflects ongoing innovation in precise molecular targeting therapies, aligning with trends toward personalized medicine.


FAQs

1. What is the significance of WO2012009706's broad chemical structure claims?
Broad structure claims allow the patent to cover multiple derivatives and analogs, increasing the patent’s scope and providing greater protection against competitors developing similar compounds.

2. How does WO2012009706 compare with existing patents in the same therapeutic area?
It likely builds upon prior art by introducing specific structural modifications or new therapeutic indications, but its novelty must be assessed in light of existing patents and publications.

3. What are the challenges in enforcing claims in this patent?
Enforcement challenges include demonstrating that a competing compound infringes within the scope of the claims and overcoming prior art objections that could invalidate parts of the patent.

4. How do patent landscape analyses inform R&D strategies?
They reveal active innovation areas, identify potential licensing opportunities, and help avoid infringement by understanding existing patent clusters.

5. What is the importance of WO2012009706's claims directed at therapeutic uses?
Use claims can be especially valuable as they provide patent protection for the application of compounds in specific medical treatments, which can be crucial in securing regulatory exclusivity.


References

  1. World Intellectual Property Organization. WO2012009706. [Online]. Available: https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2012009706
  2. Patent Landscape Reports on Pharmaceutical Patents (Various).
  3. WIPO Patent Cooperation Treaty (PCT) Guidelines.
  4. Patentability Criteria and Patent Landscape Analysis Methodology.

(Note: Actual references corresponding to specific patent citations or prior art are contextual and would be detailed based on the precise patent and literature database searches.)

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