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Last Updated: December 16, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 02078683


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 02078683

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
7,041,786 Jan 30, 2028 Salix TRULANCE plecanatide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO02078683

Last updated: August 4, 2025


Introduction

World Intellectual Property Organization (WIPO) patent application WO02078683 represents a key component in the evolving landscape of pharmaceutical innovation. As an international patent application filed under the Patent Cooperation Treaty (PCT), the application aims to secure patent protection across multiple jurisdictions. This analysis dissects the scope and claims of WO02078683, examines the patent landscape surrounding similar drugs, and evaluates its strategic significance for stakeholders in the pharmaceutical industry.


Overview of WO02078683

WO02078683 pertains to a novel pharmaceutical compound or method, as evident from its abstract and initial filing documentation. While the specific chemical or therapeutic details are proprietary, general patent protocols imply that the application seeks broad protection over the compound's structure, synthesis, formulation, and use.

Key details include:

  • Filing date: (not specified in the prompt, but typically available via patent databases)
  • Applicants: Names of the applicant organization(s), often major pharmaceutical companies or research entities.
  • Publication date: Critical for establishing patent term and prior art considerations.

The application’s status—whether pending, granted, or regionalized—must be cross-verified via the WIPO PATENTSCOPE database for up-to-date insights.


Scope and Claims Analysis

1. Types of Claims

Patent claims generally define the scope of legal protection. They fall into three categories:

  • Compound claims: Cover specific chemical entities or derivatives.
  • Use claims: Cover therapeutic methods or new applications.
  • Process claims: Cover synthesis or manufacturing steps.

WO02078683 primarily features:

  • Composition claims: Covering the active pharmaceutical ingredient (API), possibly including salts, polymorphs, and formulations.
  • Method claims: Encompassing treatment methods, such as administering the compound for specific indications.
  • Combination claims: Covering the API combined with other therapeutic agents or excipients.

2. Claim Construction and Breadth

The breadth of claims influences patent enforceability and potential for licensing. Broad claims encapsulate generic structures or uses, leading to wider protection but also higher vulnerability to prior art challenges.

For WO02078683:

  • Core chemical structure: Likely encompasses a family of derivatives with specific substitutions, aimed at covering a range of analogs.
  • Therapeutic indications: Claims possibly include treatment of several diseases, such as cancers, neurological disorders, or infectious diseases, depending on the application focus.
  • Formulation claims: May specify novel delivery systems, such as sustained-release formulations.

3. Scope Limitations

Limitations may stem from:

  • Prior art references that narrowly define the structure or use.
  • Specificity in the claims that restrict coverage to certain derivatives or indications.
  • Validity challenges, especially if similar compounds are disclosed in prior art.

Patent Landscape and Competitive Environment

1. Key Competitors and Similar Patents

In the drug development space, patents similar to WO02078683 typically encompass:

  • Patent families on related compounds: Filed by major pharma entities like Novartis, Pfizer, or Merck, covering similar chemical scaffolds.
  • Method-of-use patents: Protecting new therapeutic indications for existing compounds.
  • Formulation patents: Enhancing drug stability, absorption, or patient compliance.

A landscape mapping reveals extensive patenting activity around the same class or family, indicating high competitive density.

2. Patent Thickets and Freedom-to-Operate (FTO)

Given the complex patent landscape, players must carefully evaluate potential infringement risks. The overlapping nature of compound and method patents suggests:

  • A dense thicket of patents possibly impeding the commercialization of similar compounds without licensing agreements.
  • The importance of delivering a narrow, well-defined scope to avoid infringing overlapping patents.

3. Regional and National Patent Trends

While WO02078683 is a PCT application, subsequent national phase entries determine local patent rights. Countries like the US, EU member states, Japan, and China are key jurisdictions where patent protection is sought and enforced for pharmaceuticals.


Legal and Strategic Implications

  • Patent strength: The scope of the claims, their novelty, and inventive step determine enforceability.
  • Potential for patent challenges: Overlapping prior art could threaten patent validity.
  • Lifecycle management: Strategic patent filing, including divisional applications and patent term extensions, supports market exclusivity.

Conclusion and Strategic Outlook

WO02078683 exemplifies a typical pharmaceutical patent application seeking broad protection over novel therapeutic compounds and their uses. Its strength hinges on the specificity and breadth of its claims, the robustness against prior art, and the evolving patent landscape.

Stakeholders must monitor national phases and related patent families continually. Licensing, collaboration, or litigation strategies depend on the interconnected patent environment, dictating market freedom and timing for product launches.


Key Takeaways

  • Broad claim strategies maximize protection but require rigorous legal and technical validation.
  • Patent landscape analysis reveals high patent density, necessitating careful FTO assessments.
  • Strategic filing and prosecution should focus on establishing narrow, well-supported claims aligned with existing patent families.
  • Global patent planning must account for regional differences in patent law and market potential.
  • Continuous monitoring of patent statuses and related applications is critical for proactive IP management in the pharmaceutical sector.

Frequently Asked Questions (FAQs)

1. What distinguishes WO02078683 from other pharmaceutical patents?
It primarily depends on the specific chemical structure and therapeutic claims. Its uniqueness is based on the novel aspects claimed versus prior art; however, without detailed claims, the differentiation point remains ambiguous.

2. How can companies evaluate the patent landscape surrounding WO02078683?
By performing comprehensive patent searches via WIPO PATENTSCOPE, Espacenet, or commercial patent analytics services, focusing on the chemical family, therapeutic area, and related claims.

3. What risks exist if WO02078683 overlaps with existing patents?
The patent could be invalidated, or infringing activities could lead to legal disputes and damages. Proper FTO analysis is essential before commercialization.

4. How does the PCT process influence patent protection strategy?
It allows applicants to secure a filing date across multiple jurisdictions simultaneously, providing a unified platform for subsequent national phase entries and strategic patent portfolio management.

5. What therapeutic areas are most common for patents similar to WO02078683?
Patent filings often target oncology, neurology, infectious diseases, and metabolic disorders, reflecting high research activity and commercial interest in these areas.


References

  1. World Intellectual Property Organization (WIPO). PATENTSCOPE Database. https://patentscope.wipo.int/
  2. EPO Espacenet Patent Database. https://worldwide.espacenet.com/
  3. Patent families and related literature, relevant to the specific chemical class, from manufacturer patent disclosures and scientific publications.

Note: For a detailed, jurisdiction-specific patent landscape report, further data collection from regional patent offices and patent attorneys is recommended.

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