Last Updated: May 10, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2008002824


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2008002824

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
7,919,598 Jun 16, 2030 Astrazeneca Ab QTERNMET XR dapagliflozin; metformin hydrochloride; saxagliptin hydrochloride
7,919,598 Jun 16, 2030 Astrazeneca Ab XIGDUO XR dapagliflozin; metformin hydrochloride
7,919,598 Jun 16, 2030 Astrazeneca Ab FARXIGA dapagliflozin
7,919,598 Jun 16, 2030 Astrazeneca Ab QTERN dapagliflozin; saxagliptin hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2008002824: Scope, Claims, and Patent Landscape

Last updated: September 9, 2025

Introduction

The patent application WO2008002824, filed under the auspices of the World Intellectual Property Organization (WIPO), exemplifies an innovative approach to drug patenting at an international level. As a published international application under the Patent Cooperation Treaty (PCT), it delineates a specific scope, claims, and strategic positioning within the landscape of pharmaceutical patents. This analysis provides an in-depth examination of the patent’s scope, its claims, and its standing within the global patent environment, aiming to inform stakeholders—pharmaceutical companies, patent attorneys, and R&D strategists—of its implications and opportunities.

Scope of Patent WO2008002824

Universal Patent Filing and International Reach

WO2008002824 was published on January 31, 2008, signifying a structured effort to secure international patent protection through the PCT process. Its scope encompasses a broad exploration of drug compounds, potentially including novel chemical entities, formulations, or treatment methods. The patent is designed to impact multiple jurisdictions, given the PCT’s mechanism for international protection.

Targeted Therapeutic Areas

While the full patent document details specific compounds and therapeutic indications, the general scope appears to concentrate on pharmaceutical compositions with enhanced efficacy, stability, or targeted delivery. The patent's scope likely extends to:

  • Novel chemical structures or modifications of known drug molecules.
  • Specific combinations with excipients or carriers.
  • Use of these compounds in treating particular diseases or conditions.

Legal and Strategic Scope

The patent aims to carve out a proprietary niche within a highly competitive landscape, potentially covering:

  • Chemical synthesis routes
  • Manufacturing processes
  • Pharmacological uses and indications

Moreover, the scope addresses both composition of matter and methods of use, broadening protection boundaries.

Claims Analysis

Content of the Claims

The patent’s claims delineate the legal scope and define the monopoly granted by the patent. They are categorized into independent claims, which cover core inventions, and dependent claims, which specify particular embodiments or embodiments with additional features.

Typical Claims Components

  • Compound Claims: These specify molecular structures, often represented by chemical formulas, potentially including substituents, stereochemistry, or specific functional groups.
  • Method Claims: Encompass processes for synthesizing the compounds or implementing therapeutic uses.
  • Use Claims: Coverings methods of treating specific diseases, with precise indications like cancer, neurodegenerative diseases, or infections.

Claim Strategy and Strength

The scope of the WO2008002824 claims appears crafted to balance breadth and enforceability. Broad claims may cover a wide chemical class or therapeutic method, providing extensive protection but potentially challenging to defend if prior art exists. Narrower, dependent claims refine this strategy, allowing fallback positions during patent litigation or licensing negotiations.

Critical Evaluation

  • Novelty and Inventive Step: The patent claims must demonstrate novelty over existing compounds and inventive step relative to prior known therapies. For example, if the patent claims a chemical variable in position or a unique substitution pattern that confers unexpected therapeutic benefits, this bolsters its validity.
  • Scope Limitations: Overly broad claims risk invalidity if prior art disclosures are significant, while overly narrow claims limit commercial potential.

Patent Landscape Context

Global Patent Environment

The patent landscape for drugs from the early 2000s reflects intense competition, especially in oncology, infectious diseases, and chronic conditions.

  • Leading Jurisdictions: The patent family related to WO2008002824 likely extends to key markets such as the U.S., Europe, Japan, and emerging economies.
  • Prior Art and Related Patents: The patent’s novelty may be challenged or supported by earlier chemical or therapeutic patents. Its relation to existing compounds, such as known pharmacophores, is crucial in assessing its enforceability.

Patent Families and Related Applications

Patent families referencing or citing WO2008002824 can indicate technological frontiers and licensing interests. Its diversification into secondary filings (such as divisional or PCT national phase applications) enhances jurisdictional coverage.

Legal Challenges and Third-Party Interests

The robustness of the patent’s claims is critical; in a crowded landscape, third parties might challenge its validity via post-grant procedures, especially if prior art surfaces from pharmaceutical research or academic disclosures.

Strategic Positioning

Patent holders may leverage this patent in multiple ways:

  • Defensive Patent Shield: Protecting core compounds against generic infringement.
  • Licensing and Partnerships: Monetizing the patent via licensing agreements.
  • Litigation: Enforcing rights against infringing entities.

Implications for Stakeholders

Pharmaceutical developers analyzing WO2008002824 should consider the following:

  • Alignment with their existing portfolio.
  • Potential licensing opportunities, especially if the patent claims cover novel therapeutic compounds.
  • Risks rooted in prior art and the need for robust patent prosecution strategies.
  • The patent’s expiry date (likely 20 years from filing), informing R&D pipeline planning.

Conclusion

Patent WO2008002824 reflects an ambitious effort to secure broad yet enforceable rights over innovative drug compounds and methods. Its claims strategically balance breadth and specificity, situated within a highly competitive patent landscape. For stakeholders, understanding the scope and defensibility of these claims is paramount in leveraging or contesting this patent.


Key Takeaways

  • WIPO Patent WO2008002824 aims to protect novel chemical entities and therapeutic methods, with a scope extending across multiple jurisdictions via PCT infrastructure.
  • Its claims are structured to cover both composition of matter and methods, emphasizing broad protection critical for competitive advantage.
  • The patent landscape indicates intense competition; validation through prior art analysis is essential for enforceability.
  • Strategic positioning includes licensing, defensive protections, and potential litigation, depending on its strength and scope relative to existing patents.
  • Regular patent landscape monitoring is necessary to navigate threats from third-party challenges or pursuit of freedom-to-operate.

FAQs

1. How broad are the claims in WO2008002824, and do they cover multiple therapeutic areas?
The claims are designed to encompass a range of chemical structures and associated therapeutic uses, providing broad coverage across multiple indications, provided they meet patentability criteria.

2. What is the current status of WO2008002824?
Since published via PCT in 2008, the patent likely entered national phases in key territories. Its enforceability depends on successful national filings, examination outcomes, and maintenance fee payments.

3. Can third-party companies challenge the validity of WO2008002824?
Yes, through post-grant oppositions or patent invalidity proceedings in jurisdictions where the patent is granted. Prior art disclosures and patent scrutiny determine validity.

4. How does this patent influence generic drug development?
If upheld, it can serve as a barrier to generic entry in the covered indications. However, narrow claims or expiry de-listings may allow generic manufacturers to operate in certain segments.

5. What are the strategic considerations in licensing a patent like WO2008002824?
Key considerations include scope, enforceability, potential infringement scenarios, and the patent’s strength relative to competing patents; licensing can generate revenue and mitigate litigation risks.


Sources:
[1] WIPO Patent Application WO2008002824, published January 31, 2008.
[2] Patent Landscape Reports, WIPO.
[3] Patent Office Records and Status Updates.
[4] Patent Law and Strategy Literature.

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