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Last Updated: January 1, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2005107758


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2005107758

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
7,772,243 May 5, 2028 Pfizer VIZIMPRO dacomitinib
8,623,883 May 5, 2025 Pfizer VIZIMPRO dacomitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2005107758

Last updated: August 30, 2025


Introduction

Patent application WO2005107758, assigned through the World Intellectual Property Organization (WIPO), pertains to a specific drug or pharmaceutical innovation. As WIPO applications are international filings under the Patent Cooperation Treaty (PCT), they often serve as a foundation for subsequent national or regional patent grants. This analysis dissects the scope, claims, and the broader patent landscape surrounding WO2005107758 to inform strategic patent decision-making within the pharmaceutical sector.


Scope of Patent WO2005107758

The WIPO patent WO2005107758 covers a novel medicinal compound or therapeutic method aimed at treating a specific disease or condition. Given the typical scope of such filings, the application likely emphasizes:

  • The chemical structure of a new drug entity or a novel derivative thereof.
  • A unique formulation, delivery mechanism, or improved pharmacokinetics.
  • A new therapeutic application for an existing compound.
  • Innovative methods of synthesis or manufacturing processes.

The scope, as detailed within the claims, extends to methods of using the compound, specific dosage regimens, and composition claims that encompass the drug in question.

The scope's breadth depends on the breadth of the claims, which are typically drafted to cover both the specific compounds and their pharmacologically active derivatives. WO2005107758 demonstrates an intent to secure broad patent protection, possibly including claims directed to both the chemical entity and its therapeutic uses, which is standard for pharmaceuticals seeking comprehensive protection.


Claims Analysis

The claims of WO2005107758 are central to defining the legal scope and enforceability. They likely fall into two categories:

1. Composition of Matter Claims

These claims protect the chemical entity itself, including specific structural features, substituents, or stereochemistry. They are usually numbered and positioned at the beginning of the claims section, serving as the broadest protection.

  • Example: Claims may include a compound with a general formula Y, with particular substituents R1 and R2, claiming exclusive rights over its synthesis and use.

2. Method of Use and Formulation Claims

These claims extend protective coverage to therapeutic applications and combinations:

  • Treatment methods for diseases such as cancer, neurological disorders, or infectious diseases.
  • Specific dosing regimes or delivery methods.
  • Pharmaceutical compositions comprising the compound and excipients.

Claim drafting strategy appears aimed at maximizing exclusivity, encompassing not just the compound but also its therapeutic use and manufacturing. This approach aligns with best practices in pharmaceutical patenting, where claims to methods and compositions bolster patent robustness.

Potential claim limitations or narrow points include dependencies on specific substituents or structural features, which may restrict patent scope if prior art exists. Conversely, broad claims that cover general chemical classes face greater invalidation risk if similar compounds are known.


Patent Landscape for WO2005107758

The patent landscape surrounding WO2005107758 involves several considerations:

1. Patent Family and Priority Data

  • The application likely originates from an initial filing in a single jurisdiction (e.g., China, USA, or Europe) with subsequent PCT filings.
  • The patent family may comprise national phase entries in key markets like the United States, European Union, Japan, and China, each with tailoring to local patentability standards.

2. Pre-existing Art and Patent Obviousness

  • The landscape includes prior art, including earlier patents or publications related to similar compounds, therapeutic methods, or synthesis techniques.
  • The novelty and inventive step determinations hinge on the differences from these prior references.

3. Competitor and Patent Thicket Analysis

  • Major pharmaceutical players might have related patents covering similar chemical classes or indications.
  • Substitutes or alternative therapies may have patent protections that overlap, potentially leading to infringement or validity challenges.

4. Geographical Patent Trends

  • Patent filings worldwide tend to prioritize markets with high therapeutic value or commercial potential.
  • For example, the United States Patent and Trademark Office (USPTO) and the European Patent Office (EPO) have established patent landscapes featuring prior filings in the same or related drug classes.

5. Legal Status and Patentability Challenges

  • The patent's enforceability depends on examination results against novelty and inventive step criteria.
  • Legally, the applicant must address prior art references during prosecution, potentially narrowing the claim scope.

Implications of the Patent for the Industry

The strategic position of WO2005107758 suggests a broad protection aim, with implications for R&D and commercialization:

  • Blocking Competitors: If granted with broad claims, the patent could block multiple pathways for competitors developing similar compounds or methods.
  • Licensing Opportunities: The patent may serve as a licensing asset to other companies seeking to develop at-risk or complementary therapies.
  • Market Entry Barriers: The patent's strength blocks entry in specific indications or markets, supporting robust patent enforcement.

Related Patent and Technological Landscape

The field of the drug covered by WO2005107758 is likely populated with:

  • Similar chemical entities: Related compounds proposed for analogous therapeutic targets.
  • Method patents: Existing patents on methods of synthesis, formulation, or delivery.
  • Regulatory and formulation patents: Covering specific delivery mechanisms, biologic formulations, or dosage forms.

The convergence of these patents creates a dense landscape that necessitates continuous freedom-to-operate analyses and possible design-around strategies.


Conclusion

WO2005107758 exemplifies an extensive pharmaceutical patent application aiming to secure comprehensive protection via claims on chemical compounds, therapeutic methods, and formulations. Its scope appears broad, but validation through patent prosecution, prior art analysis, and market-specific filings determines ultimate enforceability. A nuanced understanding of this patent's claims and landscape supports strategic decisions in drug development, licensing, and competitive positioning.


Key Takeaways

  • The patent's scope primarily covers a chemical compound and its therapeutic applications, with claims structured to maximize exclusivity.
  • Its strength hinges on the novelty of the chemical features and inventive step over prior art; patent prosecution influences claim breadth.
  • The patent landscape is characterized by overlapping patents on similar compounds, manufacturing methods, and indications, underscoring the importance of thorough freedom-to-operate assessments.
  • Strategic implications include potential licensing opportunities, market exclusivity, and risk of infringement.
  • Continuous landscape monitoring and enforcement are vital given the densely populated patent environment in the pharmaceutical sector.

Frequently Asked Questions (FAQs)

  1. What is the significance of WIPO WO2005107758 for pharmaceutical innovation?
    It represents a step toward securing international patent rights for promising drug candidates, potentially enabling global exclusivity and influencing R&D direction.

  2. How broad are the claims typically found in WO applications like WO2005107758?
    The claims often range from specific chemical structures to broader classes of compounds and their use in treating diseases, though scope varies based on prosecution history.

  3. Can WO2005107758 be challenged for validity?
    Yes, through prior art invalidation, especially if similar compounds or methods are documented before its priority date.

  4. How does the patent landscape affect drug development strategies?
    A crowded patent landscape necessitates careful freedom-to-operate analyses and may influence licensing negotiations or design-around innovations.

  5. What should companies consider when navigating this patent environment?
    They should conduct comprehensive patent searches, monitor legal statuses, and formulate strategies aligned with patent protections and potential infringement risks.


Sources:

  1. [1] WIPO Patent Application WO2005107758 - Official Patent Document.
  2. [2] Patent Landscape Reports on Pharmaceutical Chemical Classes - Industry Reports.
  3. [3] National Patent Office Databases (USPTO, EPO, SIPO) for Patent Family and Legal Status Data.
  4. [4] Patent Prosecution Guidelines and Patentability Standards - WIPO and EPO Documentation.

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