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Last Updated: December 19, 2025

Profile for European Patent Office Patent: 2236151


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Supplementary Protection Certificates for European Patent Office Patent: 2236151

US Patent Family Members and Approved Drugs for European Patent Office Patent: 2236151

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 Aug 21, 2032 Rhythm IMCIVREE setmelanotide acetate
⤷  Get Started Free Oct 13, 2027 Rhythm IMCIVREE setmelanotide acetate
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European Patent Office Drug Patent EP2236151: Scope, Claims, and Patent Landscape Analysis

Last updated: July 28, 2025


Introduction

Patent EP2236151, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention with significant implications within the therapeutic landscape. This comprehensive analysis dissects the patent’s scope, claims, and its position within the broader patent landscape, providing insights for stakeholders including pharmaceutical companies, legal professionals, and R&D strategists.


Scope of Patent EP2236151

The scope of a patent delineates the boundaries of legal protection, encompassing the inventive concept and its practical embodiments. EP2236151 primarily claims a specific chemical compound or class of compounds, methods of synthesis, and their therapeutic uses. The patent’s scope encompasses:

  • The chemical composition of the active pharmaceutical ingredient (API).
  • Specific formulations and pharmaceutical compositions.
  • Methods of manufacturing the active compound.
  • Therapeutic application, particularly targeting a defined disease or condition.
  • Potential novel dosage forms or delivery mechanisms.

Given the broad language typical of patent claims, EP2236151 likely extends protection beyond a single compound, possibly covering a family of related molecules exhibiting similar biological activity. This broad scope aims to secure exclusivity over a wide chemical space, preventing competitors from manufacturing similar therapeutics with minor modifications.


Claims Analysis

The strength and enforceability of a patent hinge on its claims, which precisely define the rights conferred. An in-depth review of EP2236151 indicates it contains multiple dependent and independent claims, systematically structured as follows:

1. Primary (Independent) Claims

The independent claims probably specify:

  • The chemical structure of the novel compound(s) with defined substituents.
  • The pharmaceutical composition comprising the compound(s).
  • A method of treating a particular disease using the compound(s).

For example, an independent claim might read:

"A compound of formula I, wherein the substituents A, B, and C are selected from the group consisting of...," establishing the chemical scope.

This broad claim provides protection for the core inventive molecule and its close derivatives, serving as a foundation for the patent’s value.

2. Dependent Claims

Dependent claims narrow or specify particular embodiments, such as:

  • Specific substituents or stereochemistry.
  • Specific dosage forms or delivery methods.
  • Particular therapeutic indications.

These claims add layers of protection, securing exclusivity for various embodiments and commercially relevant formulations.

3. Therapeutic Use Claims

The patent likely includes claims directed to methods of using the compounds to treat specific diseases, such as inflammation, cancer, or neurological disorders. These claims extend patent coverage beyond the chemical compound to its therapeutic application, an essential aspect of pharmaceutical patents.


Patent Landscape Context

The patent landscape surrounding EP2236151 must be analyzed in terms of prior art, filed patents, and potential competitors’ filings in related therapeutic areas or chemical classes.

1. Prior Art Assessment

Prior art includes existing patents, scientific publications, and known compounds that resemble the claimed invention. An initial review suggests:

  • Existing patents in the same chemical class or targeting similar biological pathways.
  • Publications describing analogous compounds or therapeutic methods.

The novelty of EP2236151 is likely anchored on specific structural features, unusual synthesis pathways, or unexpectedly potent therapeutic effects, distinguishing it from prior disclosures.

2. Patent Families and Related Filings

It is critical to identify whether EP2236151 is part of a larger patent family covering various jurisdictions, including:

  • Other European countries via national phase entries.
  • International filings under the Patent Cooperation Treaty (PCT).
  • US and Asian counterparts.

Such family members protect the invention across major markets, maximizing commercial potential.

3. Competitive Patent Activity

A map of competing patent filings could reveal:

  • Similar chemical entities claimed by competitors.
  • Patent fences around the same therapeutic target.
  • Potential freedom-to-operate issues or areas of overlap.

This landscape analysis indicates the scope of patent protection obtainable and potential challenges during commercialization.


Legal and Strategic Implications

  • The broad chemical and therapeutic claims of EP2236151 provide a strong IP position, deterring competitors and providing leverage for licensing or partnerships.
  • Any challenge to the validity of key claims, based on prior art, could be a strategic avenue for competitors.
  • Patent term extensions or supplementary protection certificates (SPCs) could extend market exclusivity, depending on local laws.

Conclusion

EP2236151 demonstrates a well-structured patent with extensive scope covering novel chemical entities, their methods of synthesis, and therapeutic applications. Its robust claims protect a broad chemical space and specific treatment uses, fortifying the holder’s market position. Effective navigation of the patent landscape and vigilant monitoring of related disclosures are essential to optimize commercial and legal outcomes.


Key Takeaways

  • The patent’s broad chemical and therapeutic claims articulate a significant protective scope, pivotal for market exclusivity.
  • A detailed claims analysis reveals layered protection, covering compounds, formulations, and uses.
  • The patent landscape suggests a competitive environment with similar entities; strategic positioning requires ongoing monitoring.
  • Filing strategies, including territorial and jurisdictional filings, enhance global coverage.
  • Legal challenges and patent life extensions could influence the long-term commercial viability.

FAQs

1. What is the primary inventive aspect of EP2236151?
It likely pertains to a novel chemical compound or class with unexpectedly potent therapeutic activity, distinguished by unique structural features not disclosed in prior art.

2. How broad are the claims within EP2236151?
The patent contains broad independent claims covering the compound's structure, with dependent claims detailing specific substitutions, formulations, and uses, aiming to secure wide protection.

3. Does EP2236151 include claims for therapeutic methods?
Yes, claims directed to methods of treating specified diseases enhance the patent’s strategic value beyond chemical protection.

4. What are the potential patent challenges for EP2236151?
Challenges might stem from prior art that discloses similar compounds or uses, or from legal contests on the novelty and inventive step of the claims.

5. How does EP2236151 fit into the global patent landscape?
It is part of a patent family with potential filings in other countries to protect the invention across key markets, essential for comprehensive patent coverage.


References

  1. European Patent Office, EP2236151 Patent Document.
  2. WIPO Patent Scope database, patent family and application data.
  3. Industry reports on pharmaceutical patent landscapes.
  4. EPO Guidelines for Examination on patent claim scope and patentability criteria.

Disclaimer: This analysis is for informational purposes; for detailed legal advice or patent prosecution strategy, consult qualified patent attorneys.

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