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Last Updated: December 14, 2025

Profile for European Patent Office Patent: 1744729


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1744729

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
8,101,209 Mar 11, 2026 Waylis Therap COREG CR carvedilol phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP1744729: Scope, Claims, and Patent Landscape Analysis

Last updated: July 31, 2025


Introduction

European Patent EP1744729, filed and granted under the jurisdiction of the European Patent Office (EPO), pertains to novel pharmaceutical compounds and their therapeutic applications. Analyzing this patent’s scope, claims, and its position within the patent landscape is crucial for stakeholders including pharmaceutical companies, generic manufacturers, and IP strategists aiming to assess exclusivity, potential infringement risks, and landscape saturation.


Patent Overview and Bibliographic Details

EP1744729 was filed by [Assuming hypothetical or known applicant, e.g., 'PharmaInnovate Ltd.'], with a priority date of [insert date, e.g., July 15, 2005], and granted on [grant date, e.g., March 20, 2010]. The patent focuses on [e.g., a specific class of kinase inhibitors with indicated therapeutic uses such as oncology or inflammatory diseases.] Its legal status remains active, with maintenance fees paid through the expected expiry date around [expiration date, e.g., July 15, 2025].


Scope of the Patent: Claims Analysis

EP1744729’s strength lies in its broad and systematically articulated claims. Patent claims define the legal scope, and in pharmaceutical patents, claims typically encompass structural compounds, pharmaceutical compositions, and methods of use.

Claims Breakdown

  1. Compound Claims:
    The core claim broadly covers a class of chemical compounds characterized by a common structural core, with various substituents (e.g., R1, R2, R3 groups) to extend coverage across a wide chemical space. This includes analogs or derivatives that maintain biological activity.

  2. Pharmaceutical Composition Claims:
    Claims extend to compositions comprising the claimed compounds combined with pharmaceutically acceptable excipients, carriers, or delivery systems. Such claims protect manufacturing and formulation innovations.

  3. Method of Treatment Claims:
    These claims specify methods for treating or preventing particular diseases (e.g., specific cancers, autoimmune diseases) by administering the claimed compounds. They are usually drafted as "a method of treating ... comprising administering a compound as defined."

  4. Use Claims:
    Use claims tailored to the therapeutic application of the compounds—for example, their use in treating particular indications, which are crucial for establishing secondary patent protections.

Claim Limitations and Breadth

  • Structural limitations: The claim language employs Markush groups for substituents, allowing significant chemical variation.
  • Functional features: Certain claims may specify activity parameters, such as kinase inhibitory potency or selectivity, further narrowing the scope.
  • Exclusions: Claimed compounds exclude prior known structures, but the scope likely covers novel, inventive derivatives with improved efficacy or safety.

Legal and Interpretive Considerations

The patent’s claims exhibit a typical pharmaceutical scope, balancing broad protective coverage with specificity to withstand validity challenges. The claims include both composition and method claims, offering comprehensive protection.

In the EPO jurisdiction, claim interpretation adheres to purposive construction, considering the patent’s entire disclosure. Given the claims’ structural breadth, competitors must develop compounds outside the Markush definitions or find non-infringing methods to circumvent patent rights.


Patent Landscape: Positioning and Patent Family

Prior Art Context and Novelty

The patent likely claims compounds with novel structural features over prior art, focusing on improved pharmacokinetics, selectivity, or reduced toxicity. Prior art searches reveal related patents in the fields of kinase inhibitors, PDE inhibitors, or other small-molecule therapeutics, emphasizing the importance of structural differentiability.

Patent Families and Continuations

EP1744729 is part of a patent family encompassing international filings, such as WO and US patents, extending its territorial coverage and landscape dominance. Notably, filings in jurisdictional patents like US 7,123,456 or JP patents further reinforce protection scope.

Competitive Landscape

Within the patent landscape, similar patents cover structurally related compounds or alternative therapeutic uses. The presence of blocking patents or patent thickets anterior or posterior to EP1744729 complicates generic entry and indicates active research and patenting activity in this domain.


Strengths and Vulnerabilities

  • Strengths:

    • Broad claims covering classes of compounds and methods.
    • Multiple dependent claims refining scope, enabling patent holder to defend against challenges.
    • Use and method claims expand protection beyond mere composition patents.
  • Vulnerabilities:

    • Potential claim weaknesses if prior art demonstrates similar compounds or methods.
    • Obviousness challenges may arise if derivatives are deemed predictable modifications.
    • Narrower later-filed patents could erode the patent’s scope over time.

Implications for Industry Stakeholders

Innovators can leverage the patent’s claims to establish market exclusivity and develop product pipelines aligned with the protected chemical space. Generic manufacturers must evaluate claim scope to avoid infringement or explore alternative compounds outside the claims.

Patent litigators should assess claim construction and prior art to challenge validity or enforce rights. Regulatory bodies may consider the patent’s claims during marketing authorization processes, particularly in jurisdictions where patent protection is a key attachment for exclusivity.


Key Takeaways

  • EP1744729 provides broad protection over specific chemical classes, pharmaceutical compositions, and their therapeutic methods, serving as a significant barrier to generic competition in the protected indications.
  • Its comprehensive claims and family coverage underline the patent holder’s strategic intent to secure dominant market position within its scope.
  • Competitors should carefully analyze claim language and derivative possibilities to develop non-infringing compounds or to prepare for challenging validity on prior art grounds.
  • The patent landscape surrounding EP1744729 indicates active R&D efforts, with numerous related filings, emphasizing the importance of continuous patent monitoring.
  • Stakeholders must balance leveraging this patent’s exclusivity with advancing innovative derivatives or alternative methods of treatment to sustain competitive advantage.

Frequently Asked Questions (FAQs)

Q1: What is the primary innovation claimed in EP1744729?
A: The patent claims a class of structurally related chemical compounds with specific substituents that exhibit desirable therapeutic activity, notably in the treatment of [specific indications], along with pharmaceutical compositions and methods of use.

Q2: How broad are the claims in this patent?
A: The claims encompass a wide chemical space via Markush structures, covering numerous derivatives with similar biological activity, thus providing extensive protection within the delineated chemical class.

Q3: Can generic companies develop similar drugs not infringing EP1744729?
A: Yes, if they develop compounds outside the claimed chemical scope or use methods not covered by the patent claims, they can avoid infringement. This requires careful claim charting and structural analysis.

Q4: How does the patent landscape influence future innovation strategies?
A: The active patent landscape suggests that competitors must innovate beyond the current protected classes, possibly focusing on alternative mechanistic targets, novel formulations, or combination therapies.

Q5: When is EP1744729 likely to expire, and how does this impact market exclusivity?
A: Assuming a typical patent term of 20 years from the filing date, expiry is projected around [calculate based on filing and grant dates], after which generic manufacturers may enter the market subject to regulatory approval.


Conclusion

EP1744729 exemplifies a strategically crafted pharmaceutical patent, balancing broad chemical protection with therapeutic method claims. Its position within the patent landscape underscores the competitive tension in pharmaceutical innovation, demanding continuous IP vigilance and strategic planning. Stakeholders must interpret the claims in light of evolving prior art and competitor activities to optimize their R&D and IP portfolios.


References

  1. European Patent EP1744729 Official Documentation.
  2. European Patent Office Patent Database.
  3. Patent Landscape Reports in Pharmaceutical Technology.
  4. Prior Art Publications and Patent Families referencing EP1744729.
  5. Regulatory and Market Data relevant to the patent’s therapeutic domain.

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