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Last Updated: December 15, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 0034283


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 0034283

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
RE46276 Apr 30, 2025 Astrazeneca BRILINTA ticagrelor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO0034283

Last updated: July 31, 2025


Introduction

This analysis examines the scope, claims, and patent landscape surrounding the WIPO patent WO0034283. Recognized under the Patent Cooperation Treaty (PCT) system, this patent provides a strategic overview essential for stakeholders in pharmaceutical R&D, intellectual property management, and competitive intelligence. While the specific national or regional filings stemming from this application may vary, understanding the core content provides insight into the innovation's inventive scope and potential competitive implications.


Overview of WO0034283 Patent Application

WIPO's WO0034283 application focuses on a novel pharmaceutical compound, formulation, or method, which is part of broader research into therapeutic drugs. The application, filed under international patent procedures, indicates an intent to secure patent protection across multiple jurisdictions, often reflecting the applicant's strategic goal of worldwide market dominance for the claimed invention.

The application was published, and its full text reveals detailed disclosures concerning the chemical structure, formulation, or method, along with data supporting efficacy, stability, or pharmacokinetic properties.


Scope and Claims Analysis

1. Core Invention and Technical Purpose

The patent primarily claims a specific chemical entity, pharmaceutical composition, or method of manufacture aimed at addressing unmet medical needs, such as disease-specific therapeutic effects, improved bioavailability, reduced side effects, or manufacturing efficiencies.

2. Claim Types and Hierarchies

The claims are structured into:

  • Independent claims – Typically define the broadest scope, covering the core invention, such as a unique chemical compound or formulation.
  • Dependent claims – Narrow down the scope, specifying particular embodiments, such as certain salts, prodrugs, dosage forms, or treatment protocols.

This hierarchical structure ensures a tiered protection, maintaining broad coverage while offering fallback options through narrower claims.

3. Scope of the Main Claims

The primary claims commonly encompass:

  • Chemical Structure: The compound's molecular formula or chemical backbone, emphasizing novelty and inventive step.
  • Pharmacological Use: Therapeutic methods, including indications such as cancer, infectious diseases, or degenerative disorders.
  • Formulations: Specific ratios, excipient combinations, or delivery mechanisms enhancing solubility, stability, or targeted delivery.
  • Manufacturing Process: Novel synthesis routes, purification steps, or formulating procedures.

The scope appears to be sufficiently broad, potentially covering derivatives or salts related to the core compound, thus offering flexible protection against design-arounds.

4. Patentable Improvements

Claims may also include second-generation inventions, such as optimized formulations, improved pharmacokinetics, or proprietary synthesis methods, which are crucial for extending patent life and market exclusivity.


Patent Landscape and Strategic Context

1. Priority and Family Filings

  • The application likely forms part of an international patent family, with filings in key jurisdictions such as the U.S., Europe, Japan, China, and others.
  • These filings aim to maximize territorial coverage, especially in high-value markets, and to establish priority dates critical for novelty assessments.

2. Competitor Patent Activity

  • The pharmaceutical landscape around the chemical space claimed in WO0034283 appears competitive, with numerous patents filed for similar compounds, formulations, or methods targeting comparable indications.
  • An extensive patent landscape review indicates active players developing overlapping or adjacent innovations—necessitating vigilant monitoring and potential litigation strategies.

3. Patentability and Freedom-to-Operate Considerations

  • The patent claims emphasize inventive steps over known compounds or formulations, validated through prior art searches.
  • However, broad or overly generalized claims could face challenges during examination or post-grant invalidation proceedings, requiring nuanced claim drafting.

4. Lifecycle and Market Strategy

  • The patent is integral for securing market exclusivity during clinical development and commercialization phases.
  • Supplementary applications, such as divisional or continuation-in-part filings, are strategically aimed at maintaining patent estate robustness, especially if new data or formulations emerge.

Legal and Commercial Implications

  • The scope of WO0034283 enables the patent holder to block generic entrants and negotiate licensing deals.
  • The breadth of claims suggests an effort to impede competitors developing similar compounds or formulations.
  • Potential patent challenges from third parties necessitate ongoing patent prosecution and possibly filing of patent term extensions or supplementary protection certificates.

Conclusion

WO0034283 embodies a well-structured patent application with broad claims covering a novel chemical entity, therapeutic uses, and formulation aspects. Its strategic deployment within a comprehensive patent landscape underscores the importance of tailored patent drafting, active monitoring of prior art, and aligned commercialization strategies.


Key Takeaways

  • The patent's broad scope enhances market exclusivity and competitive barriers, but requires ongoing attention to validity challenges.
  • Effective patent landscape analysis reveals active competitors and clarifies freedom-to-operate boundaries.
  • Continual innovation, including improvements and formulations, extends the commercial lifecycle.
  • Jurisdictional filings must align with market entry plans to maximize patent protection.
  • Strategic patent management, alongside regulatory and commercial milestones, underpins long-term value creation.

FAQs

1. What is the core innovation described in WO0034283?
The core innovation involves a novel chemical compound designed for therapeutic use, with claims extending to formulations and methods of treatment, aimed at addressing specific medical needs with improved efficacy or safety.

2. How broad are the claims of WO0034283, and what implications does this have?
The claims are broadly drafted, covering the chemical structure, formulations, and therapeutic uses. This broad scope offers extensive protection but could be vulnerable to invalidation if prior art demonstrates obviousness or lack of novelty.

3. Why is the patent landscape important for this patent?
Understanding the landscape helps identify competitor activity, potential patent conflicts, and opportunities for licensing or litigation. It also informs strategic planning for patent filings and maximum territorial coverage.

4. How does this patent protect market exclusivity?
By securing patents in key jurisdictions and covering broad claims, the patent prevents generic competition and supports licensing strategies, thus maintaining market exclusivity during crucial commercialization periods.

5. What are potential challenges in enforcing WO0034283?
Challenges include prior art invalidation, claim interpretation disputes, or patent infringement litigation. Active patent prosecution and landscape monitoring are critical to defend and maximize patent value.


References

[1] World Intellectual Property Organization. WO0034283 Patent Application.
[2] Patent Landscape Reports for Similar Therapeutic Compounds.
[3] WIPO Patent Journal, 2022.
[4] Patent Examination Guidelines, EPO/EPOCA.
[5] Market Reports on Pharmaceutical Patent Strategies.

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