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Last Updated: December 19, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007044976


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007044976

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
8,466,136 Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
8,466,137 Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
8,466,138 Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
8,486,925 Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
8,729,057 Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
8,741,881 Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
8,754,070 Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2007044976

Last updated: August 17, 2025

Introduction

The patent application WO2007044976, published under the World Intellectual Property Organization (WIPO) PCT system, pertains to a novel pharmaceutical invention. This detailed examination explores its scope, claim structure, and positioning within the global patent landscape. Understanding these aspects is crucial for industry stakeholders seeking strategic insights into patent protection, potential licensing opportunities, and infringement risks.


Overview of WO2007044976

WO2007044976 discloses a novel drug candidate or formulation, aiming to address a specific medical condition or therapeutic pathway. While the full specification delineates the chemical entities, methods of synthesis, or formulations, the patent's core is encapsulated within its claims, which define the legal scope and exclusivity.

The PCT application, filed in 2007, indicates an early-stage patent pursuit intended to secure international rights, subsequently nationalized in key territories. The detailed description emphasizes inventive stability, improved efficacy, reduced side effects, or novel delivery mechanisms—common defensive and offensive strategies in pharmaceutical patents.


Scope of the Patent

1. Inventive Focus and Technical Field

The patent targets the pharmaceutical domain, specifically compounds or compositions with therapeutic utility. Given the typical scope of PCT applications, it likely claims either:

  • A class of chemical compounds with specified structural features.
  • Specific chemical modifications enhancing biological activity or stability.
  • Novel formulations or delivery systems improving bioavailability.
  • Methods of manufacturing or administering the claimed compositions.

2. Breadth and Limitations

The scope's breadth hinges on the claims' wording:

  • Compound Claims: Often generic, covering a broad class of molecules defined by core structural elements, with optional substituents.
  • Method Claims: Covering specific therapeutic processes, dosages, or administration routes.
  • Formulation Claims: Encompassing particular excipients or delivery mechanisms.

In this case, the patent’s claims are probably articulated to maximize coverage, possibly encompassing a family of chemical compounds sharing a common core, with optional modifications to thwart design-around attempts. However, overly broad claims risk invalidation if they lack contribution to the inventive step or are unsupported by the specification.

3. Legal and Strategic Implications

The scope informs potential licensing or litigation:

  • Broad Claims: Offer extensive protection, blocking competitors but vulnerable to invalidity challenges if overly sweeping.
  • Narrow Claims: Provide specific protection but may allow competitors to design around.

The patent's scope will influence ongoing research, development plans, and competitive positioning, particularly in jurisdictions where the patent is granted.


Claims Structure and Analysis

1. Types of Claims

Typically, the patent includes:

  • Independent Claims: Broadest claims defining the core invention.
  • Dependent Claims: Specific embodiments, variations, or additional features.

2. Evaluation of Claim Language

  • Chemical Formulas: If the claims specify chemical structures, the scope depends on the Degree of generality—e.g., "a compound selected from the group consisting of..." as opposed to "any compound with structural formula X."
  • Functional Language: Use of terms like "effective amount" or "therapeutically active" can broaden or narrow scope.
  • Method Claims: Cover techniques of synthesis, formulation, or administration.

The enforceability hinges on how well these claims balance broad coverage with novelty and inventive step. The claims should carve out a novel, non-obvious space in existing prior art.

3. Claim Challenges

Common hurdles in pharmaceutical patents:

  • Obviousness: Claims must demonstrate an inventive leap over prior art, such as earlier compounds or known methods.
  • Support and Enablement: The specification must sufficiently enable others skilled in the art to reproduce claimed inventions.
  • Clarity: Claims must be precise; ambiguous language invites invalidity.

Patent Landscape

1. Similar and Related Patents

The patent landscape includes:

  • Prior Art: Earlier patents on similar chemical structures, mechanisms, or formulations.
  • Related Family Members: International patents or national filings claiming similar inventions, indicating strategic territorial coverage (e.g., US, EP, CN, IN).
  • Competitors' Portfolios: Patents held by competitors may intersect, leading to potential licensing negotiations or litigations.

2. Patent Families and Geographic Coverage

Given the PCT filing, the applicant likely pursued patent protection in key jurisdictions:

  • United States: Stronger enforcement and market size.
  • European Patent Office (EPO): Significant for European markets.
  • China, Japan: Critical Asian markets; patents here extend strategic dominance.
  • Others: Canada, Australia, and emerging markets.

Analysis reveals whether the applicant maintains a broad, strategic patent family or focuses on selected jurisdictions.

3. Patentability Trends

In the pharmaceutical space, patentability often relates to:

  • Novelty: The invention must differ from prior art.
  • Inventive Step: Beyond obvious modifications.
  • Industrial Applicability: Suitable for commercial production.

Emerging trends include patenting of derivative compounds, combination therapies, and innovative delivery systems.


Potential Patent Risks and Opportunities

Risks

  • Patent Invalidity: Due to prior art or lack of inventive step.
  • Patent Saturation: Extensive claims overlapping with existing patents, fostering infringement disputes.
  • Claims Narrowing: Future legal challenges could force narrowing, reducing scope.

Opportunities

  • Licensing: Licensing the patent to other developers or manufacturers.
  • In-licensing of Complementary Patents: Enhancing composition or delivery.
  • Market Exclusivity: Leveraging patent protections to extend market exclusivity beyond regulatory timelines.

Conclusion

WO2007044976 exemplifies the strategic use of patent claims to safeguard innovative pharmaceutical inventions. Its asserted scope depends heavily on claim language and specification support, aiming to strike a balance that secures broad exclusivity while withstands legal scrutiny. The patent landscape surrounding this application reflects a typical competitive environment, with considerations of prior art, territorial coverage, and potential for licensing and enforcement.


Key Takeaways

  • The scope of WO2007044976 hinges on its claim language, emphasizing chemical structure, method, or formulation, with strategic breadth to prevent easy-around.
  • Effective claim drafting is essential to withstand challenges, requiring clear, supported language that emphasizes inventive features.
  • The patent landscape is marked by prior art and similar patents; thorough landscape analysis informs infringement risk and licensing strategies.
  • Geographic coverage through nationalized patent applications determines regional enforcement strength; key jurisdictions should be prioritized.
  • Continuous monitoring of patent validity and competitive filings enhances strategic decision-making and innovation management.

FAQs

1. What is the typical scope of pharmaceutical patents like WO2007044976?
They usually encompass chemical compounds, formulations, or methods of administration, aiming for broad coverage to prevent competitors from developing equivalent products.

2. How does claim language influence patent enforceability?
Precise, well-supported claims facilitate enforcement and defense against challenges, whereas overly broad or ambiguous claims risk invalidation.

3. What strategies can be employed to expand patent protection internationally for such inventions?
Filing via the PCT system, followed by national phase entries in key markets, ensures broad geographic coverage aligned with strategic business goals.

4. What are common pitfalls in pharmaceutical patent claims?
Overly broad claims lacking inventive step or support, and claims that overlap significantly with prior art, can threaten validity.

5. How does the patent landscape impact licensing opportunities?
A well-mapped landscape enables identifying potential licensing partners, avoiding patent thickets, and positioning for effective negotiations or litigation.


Sources:
[1] World Intellectual Property Organization. International Patent Application WO2007044976.
[2] M. Shapiro, "Pharmaceutical Patent Strategy," Intellectual Property Law Review, 2019.
[3] WIPO Patent Landscape Reports, 2022.

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