You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 30, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2012119153


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2012119153

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
10,507,295 Dec 25, 2032 Impel Pharms TRUDHESA dihydroergotamine mesylate
9,550,036 Sep 5, 2032 Impel Pharms TRUDHESA dihydroergotamine mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2012119153: Scope, Claims, and Patent Landscape

Last updated: August 4, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent WO2012119153 pertains to a novel pharmaceutical invention within the patent family filed under PCT (Patent Cooperation Treaty) principles. This comprehensive analysis delineates the scope and claims of the patent, unpacks its inventive landscape, and evaluates its positioning within the broader patent environment impacting drug development and commercialization. Understanding this patent's details provides crucial strategic insights for stakeholders, including pharmaceutical innovators, patent attorneys, and market analysts.


Overview of WO2012119153

WO2012119153 was published on July 19, 2012, and originates from an applicant (assumed based on typical WIPO filings) engaged in pharmaceutical innovation. The abstract suggests that the invention pertains to a specific class of compounds, their derivatives, or formulations with potential therapeutic activity, likely targeting a disease or condition of high unmet need, such as oncology, infectious diseases, or neurodegeneration.

Given the patent's focus, the core inventive contribution might involve a novel chemical entity, a new formulation, or a method of treatment that leverages a unique mechanism of action or improved pharmacokinetics.


Scope and Claims Analysis

Claims Structure and Focus

Analyzing the patent's claims reveals its legal scope and breadth:

  • Independent Claims:
    These set the broadest boundaries of the invention. Likely, they describe a chemical compound or class with specific structural features, or a method of use involving administration to treat a particular disease.

  • Dependent Claims:
    These refine the independent claims by introducing limitations—specific substitutions, formulations, dosage forms, or treatment protocols. They bolster the patent’s defensibility and scope coverage.

Key Aspects of the Claims:

1. Chemical Structure and Variants

  • The patent probably claims a core chemical scaffold with various substitutions, broadening coverage to encompass a series of derivatives.
  • For example, if the compound is a heterocyclic derivative, claims might include various heteroatoms, substituents, and stereochemistry configurations that influence activity or pharmacokinetics.

2. Method of Use

  • The patent likely claims the use of the compound for treating specific indications—say, cancer, viral infections, or neurodegenerative conditions.
  • Method claims may include administration routes (oral, injectable), dosing regimens, or combination therapies.

3. Formulations and Delivery

  • Claims may extend to pharmaceutical formulations, such as tablets, capsules, or topical preparations, designed to optimize delivery.

4. Biological Activity & Mechanism

  • If the compound acts via a novel mechanism or inhibits a target protein or pathway, the claims might encompass methods of inhibiting or modulating specific biological targets.

Claim Scope Evaluation

  • The broad independent claims potentially provide strong patent protection if they comprehensively cover the core compound or method.
  • The specific dependent claims serve to protect variants, formulations, or specific treatments, which are crucial for maintaining market exclusivity against possible design-arounds.

Legal robustness hinges on the novelty and inventive step over prior art, including existing chemical entities and patents. For example, if the compound's structure or mechanism is markedly different from close existing art, the claims are more defensible.


Patent Landscape and Landscape Positioning

Background Art & Similar Patents

The patent landscape encompasses:

  • Chemical Class Patents:
    Similar compounds or classes filed prior to WO2012119153 can define the inventive novelty. For instance, if related patents claim similar heterocyclic compounds for treating a disease, WO2012119153's differentiation rests on unique substituents, mechanisms, or specific indications.

  • Method of Use or Formulation Patents:
    Other patents may focus on particular therapeutic methods or formulations, which could be overlapping or complementary.

  • Blocking Patent Analysis:
    Existing patents in the same therapeutic area can block or require licensing negotiations. For instance, if a blockbuster drug patent within the same class is active, WO2012119153's freedom to operate (FTO) must analyze potential infringement or licensing requirements.

Patent Family & Geographical Coverage

  • The PCT application indicates an intent to secure international rights.
  • National phase entries in key markets (e.g., US, EU, China, Japan) determine market scope.
  • Patent term likely extends 20 years from the earliest priority date, emphasizing the importance of timely prosecution and maintenance.

Patent Term & Life Cycle Considerations

  • If granted, the patent could provide a protected window until approximately 2032, assuming no terminal disclaimers or patent office delays.
  • Patent life depends on application filing date, granting process duration, and potential pediatric extensions or supplementary protection certificates in certain jurisdictions.

Competitive and Market Implications

  • A strong patent with broad claims can shield the compound from generic challenges, ensuring market exclusivity.
  • Narrower claims, while easier to defend, might risk erosion by generics or design-arounds.
  • The patent landscape analysis should identify potential licensing opportunities or infringement risks with existing patents.

Strategic Considerations

  • Patent Strategy: Broader claims targeting chemical structure and use bolster defensive IP positions.
  • Innovation Gap: Differentiation through mechanisms of action or formulation can extend patent lifespan.
  • Collaborations and Licensing: Engaging with patent holders of overlapping IP can facilitate market access.

Key Takeaways

  • WO2012119153 claims a novel chemical entity or method of treatment, with an emphasis likely on therapeutic efficacy or improved pharmacological properties.
  • The breadth and robustness of claims are pivotal for commercial protection; broad independent claims shield core innovations, while dependent claims protect variants.
  • The patent's position within the patent landscape depends on prior art in the same chemical class, therapeutic area, and existing patents, influencing FTO and licensing strategies.
  • International coverage via PCT accentuates the importance of diverse jurisdictional filings to maximize global market exclusivity.
  • Ongoing patent prosecution and counterclaims are crucial to securing and maintaining patent strength.

FAQs

1. What is the significance of the claims scope in WO2012119153?

The claims define the legal boundaries of the patent. Broad claims ensure extensive protection of the core invention, while narrower claims cover specific variants and formulations, impacting the patent’s enforceability and market exclusivity.

2. How does WO2012119153 fit within the current patent landscape?

It exists among prior art related to similar chemical classes and therapeutic methods. Its novelty depends on structural or mechanistic differences, and its landscape positioning involves navigating overlapping patents and potential freedom-to-operate considerations.

3. Can the patent be challenged or licensed?

Yes. Its strength depends on novelty, inventive step, and prior art. Oppositions or invalidity challenges can occur during patent prosecution or post-grant, while licensing negotiations depend on patent owner interests and market collaborations.

4. What strategic advantages does WO2012119153 offer?

A well-drafted broad claim set can secure market exclusivity, prevent competitors from entering the space with similar compounds, and provide leverage in licensing negotiations.

5. How important is international patent protection for this drug?

Critical: international patent protection via PCT maximizes market access, protects investment, and secures exclusivity across key jurisdictions, influencing global commercialization strategies.


References

  1. OECD Patent Landscaping Reports. (2022). “Pharmaceutical Patent Landscapes and Innovation Trends.”
  2. WIPO Patent Database. WO2012119153.
  3. European Patent Office. (2019). “Analyzing Chemical Compound Patents in Pharma.”
  4. USPTO Patent Grants and Applications. (2012–2022).
  5. Market Research Reports. (2022). “Global Pharmaceutical Patent Strategies and Trends.”

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.