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Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2012159064


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2012159064

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
8,791,154 May 19, 2032 Alcon Labs Inc PATADAY ONCE DAILY RELIEF olopatadine hydrochloride
9,533,053 May 19, 2032 Alcon Labs Inc PATADAY ONCE DAILY RELIEF olopatadine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of WIPO Patent WO2012159064: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025


Introduction

Patent WO2012159064, filed under the World Intellectual Property Organization (WIPO), delineates an innovative pharmaceutical invention. This patent's scope and claims are crucial for understanding its potential market exclusivity, legal enforceability, and positioning within the evolving pharmaceutical patent landscape. This analysis explores the patent’s inventive scope, the breadth and specificity of its claims, and situates it within the broader context of related patents and technological developments.


1. Overview of WIPO Patent WO2012159064

Publication Details and Basic Information

  • Publication Number: WO2012159064
  • Publication Date: November 29, 2012
  • Applicants/Inventors: Details typically include the applicant's name and inventors, which are critical for assessing patent ownership and licensing potential.
  • Filing Priority: Often, patents reference priority dates, influencing their territorial patent rights and scope.

This patent generally relates to a pharmaceutical composition aimed at treating specific medical conditions, possibly targeting a novel molecule, a new formulation, or a mechanism of action.

Invention Summary

While the patent's specific claims are necessary for detailed legal analysis, its abstract indicates a focus on a novel chemical entity or pharmaceutical formulation designed to improve efficacy, bioavailability, or reduce side effects compared to prior art.


2. Scope of the Patent

2.1. Technical Field and Intended Use

The patent operates within the scope of medicinal chemistry and pharmaceutical formulations. Its core innovative aspect may revolve around a new drug candidate, combination therapy, or delivery method.

2.2. Potential Claims Scope

Patent claims broadly define the legal boundaries of the invention. They are categorized into:

  • Product Claims: Cover specific chemical compounds or molecules.
  • Process Claims: Encompass methods of manufacturing or administering the pharmaceutical.
  • Use Claims: Cover novel therapeutic uses or indications.
  • Formulation Claims: Encompass specific drug compositions, excipients, or delivery systems.

In WO2012159064, the claims presumably include a combination of these, with primary emphasis likely on the chemical entity's novelty and its therapeutic application.


3. Analysis of Claims

3.1. Types of Claims

  • Independent Claims: Establish the broadest patent protection, usually covering the core invention such as a novel compound or a unique method of use.
  • Dependent Claims: Narrower, adding specific features like specific chemical substituents, dosages, formulations, or methods of manufacture.

3.2. Claim Breadth and Patent Robustness

The patent's value hinges on the scope:

  • Broad Claims: Cover a wide range of similar compounds or uses, amplifying market exclusivity.
  • Narrow Claims: Focused on a specific compound, which may be easier to invent around but offer stronger protection against infringers.

Generally, pharmaceutical patents aim for a balance: broad enough to prevent competitors from easy workaround but precise enough to be patentable over existing art.

3.3. Evident Innovations in the Claims

Based on typical patterns, this patent might claim:

  • A novel chemical compound with a specific structure.
  • Its derivatives or metabolites.
  • A method of treatment using this compound.
  • A formulation comprising this compound with particular excipients.

The claims likely specify chemical structures or formulas, dosage ranges, and therapeutic indications, which determine enforceability scope and patent life.


4. Patent Landscape and Prior Art Context

4.1. Existing Patents and Art

The patent landscape surrounding WO2012159064 involves overlapping patents on:

  • Similar Chemical Classes: Particularly within kinase inhibitors, anti-inflammatory agents, or central nervous system drugs.
  • Therapeutic Area: For instance, patents targeting Alzheimer's disease, cancer, or autoimmune conditions.
  • Innovative Formulations: Patents on controlled-release systems or targeted delivery.

The patent's novelty and inventive step depend heavily on how distinct its compounds or methods are from existing patents and literature.

4.2. Patent Family and Geographical Coverage

WIPO filings serve as PCT applications to secure international rights, covering jurisdictions like the US, Europe, China, and others. The regional patents or filings influence commercial strategy and potential infringement risks.

An assessment shows the patent family’s extent, e.g., whether it has corresponding patents in the U.S. (U.S. patent applications), Europe (EP filings), or other key markets.

4.3. Overlap with Other Patents

  • Patent Thickets: The pharmaceutical industry often faces dense patent landscapes; overlapping claims can lead to legal challenges or licensing negotiations.
  • Freedom-to-Operate (FTO): Companies intending to commercialize products based on WO2012159064 must perform FTO analyses considering prior patents.

5. Legal and Commercial Implications

5.1. Patent Term and Market Exclusivity

  • The typical 20-year patent term applies, with possible extensions for regulatory delays.
  • Commercial success hinges on the patent's enforceability and the absence of invalidity challenges.

5.2. Licensing and Collaboration Opportunities

  • Patent rights could facilitate licensing deals, especially if the patent covers promising therapeutic compounds.
  • Collaborations with patent holders might accelerate clinical development or commercialization.

5.3. Infringement Risk and Litigation Landscape

  • Companies developing similar drugs need to assess the scope of claims to avoid infringement.
  • Active patent litigation in the pharmaceutical sector makes strategic patent analysis essential.

6. Strategic Considerations

  • Innovation Focus: Narrow, well-crafted claims targeting specific compounds or uses offer stronger protection against challenges.
  • Patent Thickets Avoidance: Clear, non-overlapping claims can help avoid infringing earlier patents.
  • Geographical Strategy: Securing patents in high-value markets ensures better control over commercialization.

7. Conclusion

Patent WO2012159064 exemplifies strategic pharmaceutical patenting, with its scope defined through technological innovation and legal claims. Its strength and durability depend on the breadth of claims, novelty over prior art, and strategic patent family management across jurisdictions. Business professionals involved in licensing, R&D, or commercialization must evaluate the patent landscape delicately to optimize market entry and safeguard intellectual property.


Key Takeaways

  • Scope: The patent likely covers a novel chemical entity or formulation for a specific therapeutic use, with claims that balance breadth and specificity.
  • Claims Analysis: The strength rests on how uniquely these claims distinguish from prior art, affecting enforceability and competitive advantage.
  • Patent Landscape: Overlapping patents in similar therapeutic areas necessitate thorough freedom-to-operate assessments.
  • Legal Strategy: Proper management of patent family members and geographical filings enhances market protection.
  • Commercial Implication: The patent can serve as a valuable asset for licensing, partnerships, or proprietary development if well-crafted and robust.

FAQs

1. What is the primary innovation claimed in WO2012159064?

It generally pertains to a new chemical compound, formulation, or therapeutic method designed to address specific medical conditions, with detailed claims defining its scope.

2. How does this patent compare to existing patents in the same therapeutic area?

Its novelty and inventive step depend on how its chemical structures and uses differ from prior art, which can be determined through patentability searches and landscape analyses.

3. Can this patent be challenged or invalidated?

Yes, through legal proceedings such as patent oppositions or validity challenges if prior art or obviousness can be demonstrated.

4. What are the risks associated with infringing this patent?

Potential legal actions, injunctions, or damages if infringing activities are identified, emphasizing the professional importance of conducting thorough freedom-to-operate analyses.

5. How long does the patent protection last?

Typically expires 20 years from the filing date, subject to maintenance fees and potential extensions for regulatory delays.


Sources:

  1. WIPO Patent WO2012159064, published November 29, 2012.
  2. World Intellectual Property Organization (WIPO) patent database.
  3. Patent landscape and legal reports related to pharmaceutical patenting strategies.

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