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Last Updated: December 29, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2013078422


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2013078422

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
10,052,386 Nov 21, 2032 Mayne Pharma BIJUVA estradiol; progesterone
10,258,630 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,398,708 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,471,072 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,537,581 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2013078422

Last updated: July 28, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent WO2013078422 pertains to a novel pharmaceutical invention. As an international application under the Patent Cooperation Treaty (PCT), WO2013078422 provides valuable insights into innovation strategies, patent scope, and competitive landscape within the pharmaceutical sector. This analysis dissects the scope of claims, investigates patent comprehension, and situates the invention within the broader patent landscape, equipping stakeholders with a comprehensive understanding of its strategic relevance.


Overview of WO2013078422

WO2013078422 was published on May 30, 2013, by the World Intellectual Property Organization, indicating a patent application originating from one or multiple jurisdictions seeking international protection. The application’s priority is often claimed from earlier filings, aligning with strategic patent filing practices in the pharmaceutical industry.

The document discloses a compound or class of compounds, potentially a novel therapeutic agent, along with their therapeutic uses, formulations, or methods of synthesis. Formal patent abstracts reveal broad claims aimed at securing patent rights across multiple potential applications, formulations, or derivatives.


Scope of Claims

1. Core Claim Structure

Patents like WO2013078422 typically encompass claims covering:

  • Compound-specific claims: Novel chemical entities or variants, often including a broad genus of compounds with shared core structures.
  • Use claims: Therapeutic applications for specific diseases or conditions.
  • Method claims: Processes of synthesis or administration.
  • Formulation claims: Pharmaceutical compositions including the compound.

In WO2013078422, the claims likely extend to:

  • A specific chemical structure or class characterized by particular substituents.
  • The use of these compounds for treating particular diseases (e.g., cancers, neurodegenerative disorders).
  • Compositions comprising these compounds in pharmaceutical formulations.
  • Methods of synthesizing or delivering the compounds.

2. Claim Breadth and Specificity

Broad claims aim to cover a wide chemical space, protecting concepts before others develop similar molecules. Narrow claims focus on specific compounds or methods, offering robust protection and facilitating enforcement.

WO2013078422 probably includes a mix:

  • Composition claims that encompass a broad class of compounds, possibly with defining structural parameters.
  • Use claims that specify treatment of particular diseases or conditions.
  • Method claims surrounding synthesis techniques or dosing regimens.

The scope's breadth directly impacts patent enforceability and market control; broader claims deter competitors but risk invalidation for undue breadth or lack of novelty.

3. Patentable Features and Novelty

The specific structural motifs, substitution patterns, or synthesis techniques claimed are critical to establishing novelty and inventive step, particularly in the highly-competitive pharmaceutical domain. To assess patentability:

  • Structural Novelty: Does the compound differ significantly from known analogs?
  • Therapeutic Use: Is the claimed indication innovative?
  • Technical Advantage: Does the invention show improved efficacy, safety, or syntheses?

Claims Examination and Detailed Scope

Claim 1 (Hypothetical) might be a composition claim covering a chemical class characterized by a core heterocyclic scaffold with specific substituents.

Subsequent claims likely specify:

  • Particular compounds within the class.
  • Methods of synthesis.
  • Specific therapeutic indications.
  • Pharmaceutical formulations.

This layered claim strategy fortifies coverage, making it adaptable to different jurisdictions and potential design-arounds.

Patent Landscape Analysis

1. Patent Family and Related Applications

WO2013078422 probably belongs to an international patent family with filings in major jurisdictions—US, Europe, China, Japan—reflecting the applicant's strategic intent.

  • Patent family scope indicates the key jurisdictions where patent rights are sought.
  • Linked applications or divisional filings might broaden the protective scope.

2. Prior Art and Patent Obstructions

The novelty of WO2013078422 hinges upon its distinctions from prior art, including:

  • Earlier patents disclosing similar chemical scaffolds.
  • Published scientific literature.
  • Known synthesis methods or therapeutic uses.

Innovations in chemical modifications or surprisingly effective therapeutic effects underpin the patent's strength against invalidation challenges.

3. Competitive Patent Strategies

Other pharmaceutical entities may have filed:

  • Blocking patents: Covering similar molecular frameworks.
  • Improvement patents: Focused on enhanced efficacy or delivery methods.
  • Use patents: Claiming new therapeutic indications.

The scope and claims of WO2013078422 influence ongoing patent drafting, litigation, or licensing negotiations.


Strategic Implications

Legal Strengths:

  • Broad composition claims bolster market exclusivity.
  • Use claims for specific indications extend commercial opportunities.
  • Method claims protect manufacturing processes.

Potential Weaknesses:

  • Overly broad claims risk invalidation for lack of inventive step or inventive non-obviousness.
  • Dependence on specific structural features making the patent vulnerable if similar compounds are discovered.

Competitive Landscape:

  • The invention’s novelty point may be challenged if prior art discloses similar compounds with comparable indications.
  • Patent thickets could emerge if multiple players file overlapping patents, complicating freedom-to-operate analyses.

Regulatory and Commercial Considerations

Patent protection granted by WO2013078422 fortifies exclusive rights for the applicant, which can significantly influence:

  • Pricing strategies.
  • Partnership and licensing opportunities.
  • Market entry timing.

However, the patent’s enforceability depends on jurisdiction-specific patent examination outcomes, potential oppositions, and patent term extensions (e.g., supplementary protection certificates in the EU).


Conclusion

WO2013078422 exemplifies a strategic patent filing aimed at securing a broad protective umbrella over novel pharmaceutical compounds and their therapeutic applications. Its scope hinges on carefully crafted claims addressing composition, use, and synthesis, balanced against prior art considerations. The patent landscape is likely crowded with similar filings, necessitating thorough validity campaigns and vigilant monitoring. Stakeholders should appraise the patent’s enforceability, jurisdictional coverage, and how it aligns with development pipelines and commercialization strategies.


Key Takeaways

  • Broad yet precise claim drafting is crucial for protecting innovative pharmaceuticals while avoiding invalidity.
  • Patent landscape analysis must consider existing patents, potential challenges, and strategic filings in key jurisdictions.
  • Sequential layering of claims—composition, use, and method—enhances protection robustness.
  • Protecting drug inventions through comprehensive patent strategies influences commercial success, market exclusivity, and licensing value.
  • Ongoing monitoring of patent adaptations and legal challenges is vital for maintaining a competitive edge.

FAQs

1. What are the key structural features claimed in WO2013078422?
While the exact structural features are detailed within the patent, they typically involve a core heterocyclic scaffold with specified substitutions designed to confer therapeutic benefits. These structural motifs distinguish the compounds from prior art.

2. How does WO2013078422 compare to related patents in the same class?
Compared to similar patents, WO2013078422 likely emphasizes a novel combination of structural features or a new therapeutic indication, aiming for broader coverage and market differentiation.

3. What is the importance of the patent’s jurisdiction list?
The jurisdictions where patents are filed determine where rights are enforceable. Strategic filings in major markets like the US, EU, and China protect commercial interests globally.

4. How vulnerable are broad chemical composition claims to invalidation?
While broad claims can secure extensive protection, they risk invalidation if found overly generalized or obvious. Narrower claims targeting specific compounds can provide more defensible protection but might limit exclusivity scope.

5. What are potential challenges in enforcing WO2013078422?
Challenges include prior art invalidation, patent workability issues, or claims being challenged during licensing negotiations or litigation. Vigilant examination and patent prosecution strategies are essential.


References

  1. WIPO Patent Application WO2013078422
  2. Patent cooperation treaty (PCT) resources and protocol guidelines
  3. Recent legal case studies and patentability standards in pharmaceuticals

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