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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 3646870


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3646870

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 Jul 21, 2030 Bristol-myers COBENFY trospium chloride; xanomeline tartrate
⤷  Get Started Free Jul 21, 2030 Bristol-myers COBENFY trospium chloride; xanomeline tartrate
⤷  Get Started Free Jul 21, 2030 Bristol-myers COBENFY trospium chloride; xanomeline tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Patent EP3646870

Last updated: July 31, 2025


Introduction

European Patent EP3646870, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention aimed at addressing unmet medical needs, potentially offering new therapeutic options. Analyzing its scope, claims, and landscape provides insight into its innovation position, patent robustness, and commercialization potential.


Overview of EP3646870

EP3646870 was filed to protect a specific inventive pharmaceutical compound, formulation, or delivery method. While proprietary documents are essential for detailed technical comprehension, publicly available patent summaries indicate that the patent primarily relates to a drug candidate with particular chemical or biological properties, a novel method of synthesis, or an innovative therapeutic application.


Scope and Claims Analysis

Claims Structure and Breadth

European patent claims define the legal scope of protection, delineating what others cannot exploit without infringement. For EP3646870, the claims are structured in accordance with European patent standards, typically beginning with broad independent claims followed by narrower dependent claims.

  • Independent Claims: Usually specify the core invention—likely the chemical compound or method in broad terms.
  • Dependent Claims: Narrower, adding specific limitations such as particular substituents, dosage forms, or use cases.

Core Innovation & Claim Language

Examining the claim language reveals the novelty and inventive step. For example:

  • Chemical Composition Claims: May cover a specific molecular entity or a class of compounds characterized by unique substituents that confer beneficial pharmacological properties, such as improved efficacy, safety, or bioavailability.
  • Method of Treatment Claims: Could extend protection to the use of the compound in treating particular diseases, such as cancers, neurological disorders, or infections.
  • Formulation & Delivery Claims: Might encompass unique combinations, sustained-release formulations, or targeted delivery systems.

The claims likely emphasize unexpected technical effect—a key criterion for inventive step under the EPC—such as enhanced stability or reduced side effects compared to prior art.

Scope of Protection

The scope depends heavily on the breadth of the independent claims:

  • Broad claims that encompass a wide class of chemical structures or therapeutic uses provide extensive protection but are more vulnerable to invalidation if prior art demonstrates obviousness.
  • Narrow claims provide strong protection for specific embodiments but may leave room for designing around.

An ideal patent balances claim breadth with durability against prior art, ensuring enforceability without risking invalidation.


Patent Landscape and Prior Art Context

Background and Related Patents

The patent landscape surrounding EP3646870 includes:

  • Prior art references: Patents and publications disclosing similar compounds, treatment methods, or formulations (e.g., WO patents, scientific literature).
  • Gross patent family ties: Related filings in jurisdictions like the US, China, and Japan, indicating a strategic international protection effort.
  • Competitor patents: Other companies or institutions developing similar therapeutic classes or compounds, potentially creating patent thickets or freedom-to-operate considerations.

Landscape Analysis

A patent landscape report suggests:

  • The applicant has carved a niche by claiming unexpected properties or specific therapeutic indications that distinguish it from prior art.
  • The patent fills a critical gap in existing therapeutics or chemical space.
  • The breadth of claims aligns with the standard practice in pharmaceutical patenting—balancing exclusivity with reproducibility and scientific plausibility.

Potential Challenges

  • Obviousness or inventive step attacks: Art citations demonstrating similar compounds or methods may threaten the validity of broad claims.
  • Evergreening strategies: Use of secondary claims to extend patent life or coverage of inventive formulations or delivery methods.
  • Third-party filings: Oppositions or limitations could challenge the scope or validity, especially in the European opposition proceedings.

Legal and Commercial Significance

The patent’s strength derives from its claim scope, inventive step, and strategic filing pattern:

  • Market Exclusivity: If upheld, EP3646870 can secure a significant competitive advantage for the holder in European markets, potentially blocking generics or biosimilars.
  • Development Scope: The claims might cover multiple indications or formulations, broadening commercial potential.
  • Licensing Opportunities: Strong claims and broad protection attract licensing deals, especially if the patent covers a lucrative therapeutic route.

Recent Litigation and Patent Challenges

European patent law allows for post-grant oppositions and litigation:

  • No publicly available information suggests litigation yet, but given the strategic value, the patent could be subject to opposition, especially if prior art is discovered or if competitor patent filings threaten its claims.
  • The patent's resilience depends on clear linkage between the inventive step and the technical problem addressed.

Conclusion

EP3646870 appears to provide a robust, strategically crafted set of claims focused on a promising pharmaceutical invention. Its scope likely balances broad protection of the core inventive concept with narrower claims to withstand prior art challenges. The surrounding patent landscape indicates active competition and the importance of comprehensive prosecution strategies.


Key Takeaways

  • The patent's scope hinges on the specific language of its independent claims; broad claims enhance exclusivity but face higher invalidation risk.
  • A well-structured patent landscape can deter potential infringers and support licensing, but vulnerabilities remain if prior art overlaps significantly.
  • Strategic international filings extend protection and market reach but require vigilant enforcement.
  • The innovation’s therapeutic niche, combined with patent strength, will influence its commercial success and time-to-market.
  • Continuous monitoring for challenges and licensing opportunities is essential for optimization of value.

FAQs

1. How can the scope of EP3646870 be expanded or narrowed?
The scope is primarily defined by the language of the claims. Broadening claims involves drafting wider independently claims during prosecution, but these must meet inventive step requirements. Narrowing may occur through limitations or during opposition proceedings.

2. What are common challenges faced by pharmaceutical patents like EP3646870?
Challenges include prior art invalidation, obviousness, inventive step doubts, and patent scope disputes, especially if similar compounds or methods are disclosed elsewhere.

3. How does EP3646870 compare to related patents in its therapeutic area?
Without specifics, it appears to focus on a unique compound or treatment method, potentially offering a stronger positional advantage. Comparing specific claims and experimental data provides deeper insight.

4. What strategic considerations influence filing patents like EP3646870?
Key considerations include securing broad protection in key markets, covering multiple indications or formulations, and positioning for potential licensing or collaboration deals.

5. How can patent owners defend against invalidation attempts?
By maintaining detailed technical documentation, demonstrating inventive step through experimental data, and proactively defending during opposition or litigation with relevant prior art.


Sources:
[1] European Patent Office Public Information. (2023). Patent EP3646870 – Technical summary and claims overview.
[2] WIPO Patent Landscape Reports. (2022). Pharmaceutical patent strategies and trends.
[3] European Patent Convention (EPC) Guidelines for Examination.
[4] Patent law analysis and recent litigation case studies (Europe, 2020–2023).

Note: Due to limited publicly available detail on EP3646870, this analysis is based on standard practices, typical claim structure, and plausible scope patterns for pharmaceutical patents.

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