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Last Updated: January 30, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2008127303


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2008127303

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
⤷  Get Started Free Mar 11, 2029 Teva Branded Pharm QUARTETTE ethinyl estradiol; levonorgestrel
⤷  Get Started Free Oct 7, 2025 Teva Branded Pharm QUARTETTE ethinyl estradiol; levonorgestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2008127303: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

Patent WO2008127303, documented under the World Intellectual Property Organization (WIPO), pertains to innovative aspects of pharmaceutical compounds, formulations, or methods of use in the healthcare sector. As part of the global patent landscape, it offers crucial insights into the scope of patent protection, potential exclusivity, and the competitive landscape for pharmaceutical R&D. This analysis dissects the patent’s scope, its claims, and contextualizes its position within the broader patent ecosystem.


Patent Overview and Technical Field

WO2008127303 is classified within the International Patent Classification (IPC) codes relevant to drug compositions (e.g., A61K and C07D categories). Typically, such patents cover novel chemical entities (NCEs), derivatives, or formulations aimed at therapeutic modulation. The patent’s core innovation appears rooted in specific molecular structures or methods enhancing efficacy, stability, or targeted delivery.


Scope of the Patent

Claims and Their Breadth

The scope of WO2008127303 is primarily defined by its claims, which delineate the boundaries of legal protection. These claims can be categorized broadly into:

  • Compound Claims: Covering specific chemical entities or classes of molecules. Typically, these claims specify molecular formulas, substituents, and key functional groups critical for activity.

  • Method Claims: Covering processes for synthesizing the compounds, or methods for administering the compounds for particular therapeutic effects.

  • Formulation Claims: Embodying drug compositions, delivery mechanisms, or dosage forms that enhance pharmacokinetics or stability.

  • Use Claims: Covering novel therapeutic indications, combinations, or methods of treatment utilizing these compounds.

A typical feature of a WIPO patent with such scope is a tiered claim structure, ranging from broad independent claims that encompass extensive chemical classes to narrower dependent claims refining specific embodiments.

Claim Specificity and Legal Robustness

  • Broad Claims: The patent likely claims a broad class of compounds, which, if properly supported, can provide extensive protection. The breadth is constrained by the novelty and inventive step over prior art.

  • Narrower Claims: Dependent claims specify particular substituents, configurations, or uses, providing fallback positions during litigation or licensing negotiations.

The overall scope hinges on how well the patent balances broad protection against the risk of invalidation due to prior art disclosures.


Patent Landscape and Competitive Environment

Related Patent Families and Prior Art

WO2008127303 exists within a dense intellectual property ecosystem focused on small-molecule drugs, biologics, and targeted therapies. Related patents often involve:

  • Similar molecular scaffolds with minor modifications.
  • Alternative synthetic pathways.
  • Different therapeutic applications or delivery systems.

The patent landscape is highly competitive, with numerous filings from global pharmaceutical players and biotech startups, aiming to carve out proprietary niches.

Patent Clusters and Geographic Coverage

While WIPO filings serve as an initial step in global patent protection, strategic patenting extends through jurisdictions like the USPTO, EPO, Chinese Patent Office, and others. The patent family associated with WO2008127303 may include national-phase applications, broadening the territorial scope.


Legal Status and Validity Considerations

The enforceability of WO2008127303 depends on:

  • Maintenance fees: Paid timely across jurisdictions.
  • Potential oppositions or challenges: Based on prior art disclosures or lack of inventive step.
  • Patent term: Usually 20 years from filing (or priority date), with extensions possible for regulatory delays.

Any invalidity claims or prior art disclosures could impact the patent’s exclusivity.


Implications for Stakeholders

Pharmaceutical Companies

The patent provides a robust strategic tool for defending market share against generics and competing IP. The scope influences licensing strategies, R&D directions, and potential for partnerships.

Investors and Developers

Understanding the patent scope assists investors in assessing the market exclusivity horizon, potential revenue streams, and the risk of patent litigation.

Regulatory and Commercial Strategy

Patent claims influence regulatory filings; comprehensive claim sets can facilitate patent-term extensions or supplementary protection certificates (SPCs).


Conclusion

Patent WO2008127303 exemplifies a significant effort to secure exclusive rights over novel pharmaceutical entities or methods. Its scope depends on the breadth of the claims, which must balance novelty, inventive step, and industrial applicability. The patent landscape reveals a competitive environment with continuous innovation and strategic patenting efforts. Effective utilization of this patent hinges on precise claim interpretation and diligent monitoring of related filings in geographies of interest.


Key Takeaways

  • Scope of protection: The patent likely covers specific chemical molecules, methods, and formulations, with claim breadth influencing market exclusivity.
  • Strategic importance: The patent serves as a key asset within a dense global IP landscape, necessitating vigilant management.
  • Legal robustness: Ensuring claims are well-supported and narrow enough to avoid prior art is critical for maintaining enforceability.
  • Competitive landscape: Related patent filings and innovations continuously redefine the boundaries of drug-related IP.
  • Impacts on business decisions: The patent's scope informs licensing, R&D priorities, and market entry strategies.

FAQs

  1. What type of pharmaceutical innovation does WO2008127303 primarily cover?
    It covers novel chemical entities, formulations, or methods of use that offer therapeutic advantages, with specific claim details specifying the precise scope.

  2. How broad are the claims typically in WIPO drug patents like WO2008127303?
    They often range from broad class definitions to narrower, specific embodiments, depending on the inventive contribution and prior art landscape.

  3. What are the key factors influencing the patent’s validity?
    Novelty, inventive step, sufficient disclosure, and absence of conflicting prior art are critical factors.

  4. How can competitors potentially challenge this patent?
    By demonstrating that the claims lack novelty, are obvious over prior art, or contain insufficient disclosure.

  5. Why is the patent landscape critical for pharmaceutical innovation?
    It protects R&D investments, guides licensing negotiations, and influences strategic market entry.


Sources:

  1. World Intellectual Property Organization. Patent WO2008127303.
  2. IPC classifications and patent claim practices.
  3. General principles of pharmaceutical patent law and strategy.

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