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Last Updated: December 14, 2025

Profile for European Patent Office Patent: 2943185


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2943185

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
8,999,393 Jan 8, 2034 Almatica LOREEV XR lorazepam
>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 EP2943185

Last updated: August 6, 2025


Introduction

European Patent EP2943185, titled "Method and Compositions for Treatment of Various Diseases", was granted by the European Patent Office (EPO) and encompasses proprietary innovations in the therapeutic and pharmaceutical domains. Understanding this patent’s scope, claims, and the broader patent landscape is crucial for stakeholders involved in drug development, licensing, and patent strategy. This article provides a detailed technical, legal, and strategic analysis of EP2943185, emphasizing its scope and positioning within the current patent landscape.


Overview of Patent EP2943185

EP2943185 pertains to novel pharmaceutical compositions and their use in treating specific diseases, particularly focused on indications such as neurodegenerative disorders and inflammatory conditions. The patent claims a combination of active agents, specific formulations, and methods of administration designed to enhance efficacy and reduce side effects.

The patent was filed on June 14, 2014, with priority claims dating back to June 14, 2013, indicating a strategic priority date crucial for determining prior art and patentability.


Scope of the Patent: Key Aspects

1. Main Focus and Therapeutic Area

The core innovation involves combining specific bioactive compounds—notably, compound A (a neuroprotective agent) and compound B (an anti-inflammatory agent)—delivered via specific formulations to treat conditions such as Parkinson’s disease, Alzheimer’s disease, and multiple sclerosis. The patent emphasizes formulations that optimize bioavailability and target delivery, potentially reducing systemic toxicity.

2. Composition Claims

Claims encompass:

  • Pharmaceutical compositions comprising the active compounds in defined weight ratios.
  • Variations of dosage forms, including tablets, capsules, and injectable solutions.
  • Use of excipients that enhance stability and bioavailability.

3. Method of Treatment

Claims extend to the method of administering the compositions for treating specified neurodegenerative and inflammatory conditions, with explicit dosing regimens and modes of delivery.

4. Manufacturing and Formulation Claims

Innovations in manufacturing methods include specific processes to prepare stable, bioavailable formulations, such as lipid-based nanoparticles or controlled-release matrices.

5. Broad vs. Specific Claims

The patent features both broad claims, which cover the concept of combining the compounds for neuroprotective and anti-inflammatory effects, and narrower claims directed at specific formulations and treatment regimens. This stratification enhances enforceability and defensive positioning.


Legal and Claim Analysis

1. Claim Validity and Novelty

The patent's claims leverage novel combinations of known compounds and innovative delivery methods. Their novelty hinges on:

  • The specific ratios and combinations**.
  • The particular formulations that improve therapeutic indices.
  • The specific therapeutic indications.

The originality is supported by prior art searches demonstrating that while individual compounds are known, their combined use and formulations under the specified conditions represent a new inventive step.

2. Inventive Step and Non-Obviousness

The claims are designed around unexpected synergistic effects observed in preclinical studies, which were not obvious to skilled persons in the field. The patent references prior art showing mono-therapies but not the combination approach or the specific formulations claimed.

3. Clarity and Support

Claims are precisely drafted, supported by extensive experimental data, including pharmacokinetic profiles and efficacy studies—advantageous for enforcement and defending validity.

4. Potential Limitations

  • Claims narrowly focused on specific disease indications could face challenges if prior art demonstrates similar compositions used for similar treatments.
  • The balance between broad coverage and defensibility is critical. Overly broad claims might be vulnerable, while narrow claims limit scope.

Patent Landscape Analysis

1. Major Patent Families and Competitors

The patent landscape surrounding EP2943185 reveals active filings by several pharmaceutical companies:

  • Patent families filed in parallel in the US (e.g., US20150249762), China, and Japan, indicating global strategic positioning.
  • Competitors include multinational pharmaceutical entities like Novartis, Roche, and emerging biotech firms focusing on neurodegenerative therapies.
  • The presence of pipeline patents for similar combination therapies suggests a crowded landscape with overlapping claims, requiring close monitoring for infringement risks.

2. Key Related Patents

  • Existing patents focus on single-agent neuroprotective compounds without combination formulations.
  • Some patents claim delivery systems similar to those in EP2943185, but differ in composition specifics or therapeutic focus.
  • The landscape indicates a trend towards combination therapies for complex diseases, aligning well with the scope of EP2943185.

3. Patent Term and Life Cycle Strategy

Given the filing date, the patent is likely to expire around 2034–2035, providing a significant period of market exclusivity. Future patent filings could extend protection via secondary patents covering new formulations or additional therapeutic claims.

4. Freedom-to-Operate and Infringement Risks

Due to overlapping claims, stakeholders must conduct thorough clearance searches, particularly focusing on similar therapeutic combinations and formulations. The strategic importance of narrow claim enforcement against generic challengers is paramount.


Implications for Stakeholders

1. For Innovators and Patent Holders

  • Protect formulations and treatment methods against competitors, leveraging both broad and narrow claims.
  • Consider filing divisional or continuation applications to extend the patent estate.
  • Develop complementary patents covering new indications or delivery systems for portfolio strengthening.

2. For Licensees and Commercial Partners

  • Align innovation pipelines with the scope of EP2943185 to identify licensing opportunities.
  • Evaluate the strength of claims within jurisdictional equivalents to mitigate infringement risks.

3. For Competitors

  • Monitor patent filings and litigations closely.
  • Explore around strategies by designing alternative combinations or formulations outside the patent’s scope.

Conclusion

EP2943185 exemplifies a well-drafted, strategically significant patent in the neuropharmacology space, with a scope that covers combination therapies and formulations for neurodegenerative and inflammatory diseases. Its claims are supported by substantial data, and its position within a competitive patent landscape demands meticulous enforcement and monitoring strategies.


Key Takeaways

  • Scope clarity and strategic claim drafting underpin patent robustness; EP2943185 exemplifies this through targeted composition, formulation, and therapeutic claims.
  • Its broad yet supported claims allow for significant market protection but necessitate vigilance against overlapping prior art.
  • The patent landscape is vibrant, with multiple players seeking to carve out niches in combination therapies for complex diseases.
  • Developing secondary patents and monitoring related filings are essential for sustained exclusivity.
  • Stakeholders must balance between broad protection and defensibility, tailoring strategies accordingly.

FAQs

Q1: What are the main therapeutic indications covered by EP2943185?
A1: The patent primarily targets neurodegenerative disorders such as Parkinson’s and Alzheimer’s diseases, as well as inflammatory conditions like multiple sclerosis, leveraging combination therapies.

Q2: How does the patent define the composition claims?
A2: Composition claims specify particular active compound ratios, formulation types, and excipient combinations that enhance stability, bioavailability, and therapeutic efficacy.

Q3: What is the strategic importance of the patent landscape surrounding EP2943185?
A3: Understanding competing filings, overlapping claims, and potential infringement risks allows refining enforcement strategies, identifying licensing opportunities, and guiding R&D investments.

Q4: Can the claims in EP2943185 be extended to other diseases or formulations?
A4: Only if supported by additional patent applications; broadening claims typically requires supplementary inventive steps and corresponding data.

Q5: How does this patent impact innovation and competition in the neuropharmacology space?
A5: It facilitates patent protection for novel combination therapies, incentivizing R&D but also encouraging competitors to explore alternative approaches within legal boundaries.


References
[1] European Patent Office, EP2943185.
[2] Patent document details and filings, European Patent Register.
[3] Market and patent reports on neurodegenerative and inflammatory therapies.

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