You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 31, 2025

Profile for Spain Patent: 2705726


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Spain Patent: 2705726

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
10,300,054 Aug 23, 2031 Alkermes Inc LYBALVI olanzapine; samidorphan l-malate
10,716,785 Aug 23, 2031 Alkermes Inc LYBALVI olanzapine; samidorphan l-malate
11,185,541 Aug 23, 2031 Alkermes Inc LYBALVI olanzapine; samidorphan l-malate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2705726

Last updated: September 2, 2025

Introduction

Patent ES2705726, granted in Spain, encapsulates innovative aspects of pharmaceutical technology. As part of its strategic significance, understanding its scope, claims, and position within the patent landscape offers insights into its potential value, enforceability, and competitive impact. This analysis provides a comprehensive overview, aiming to inform business decisions, licensing potential, and R&D strategy.

Patent Overview and Technical Field

ES2705726 pertains to a novel pharmaceutical composition or process, likely related to drug formulation, delivery systems, or specific therapeutic compounds, consistent with Spain's patent classification system. While detailed technical disclosures would be extracted from the patent description, the focus here remains on intangible boundaries — scope and claims — which are crucial for assessing the patent's breadth and enforceability.

Scope of the Patent

The scope of ES2705726 hinges on its claims, which delineate the legal boundaries of the invention. Broad claims confer extensive exclusivity, while narrower claims limit patent protection but improve defendability.

Type of Patent

ES patents generally follow EU standards, emphasizing both novelty and inventive step. This patent appears to protect a specific pharmaceutical composition or process, contained within claims that are tightly drafted to balance scope and enforceability.

Claim Categorization

  • Independent Claims: Likely focus on the core inventive concept – for example, a unique formulation, a method of manufacturing, or a combination of active compounds.
  • Dependent Claims: Add specific limitations, such as particular dosage ranges, excipient compositions, or process parameters, thereby narrowing scope but strengthening validity.

The precise scope depends on the language used, which, in pharmaceutical patents, often involves chemical formulas, method steps, or composition descriptions.

Breadth and Limitations

  • Chemical Formula Claims: If the patent claims a new compound or class of compounds, the scope may be broad, covering derivatives or analogues consistent with the disclosed structure.
  • Method Claims: Cover specific processes, with scope defined by steps disclosed.
  • Use or Therapeutic Claims: Protect specific medical applications, which may limit the scope compared to composition claims but are strategically valuable.

In pharmaceutical patents, scope is frequently constrained by prior art disclosures and the specificity of claims.

Claims Analysis

While the full text of ES2705726 is necessary for an in-depth review, typical claims analysis involves scrutinizing the following:

  • Claim Language Clarity: Precise language ensures enforceability. Ambiguous terms risk invalidation or scope reduction.
  • Claim Hierarchy: Independent claims establish core invention scope; dependent claims refine or add to this.
  • Novel Features: The claims emphasize features distinguished from prior art, such as a unique combination of excipients or a particular manufacturing process.

Hypothetical Claim Structure

  • "A pharmaceutical composition comprising [specific active ingredient] and [specific excipients], wherein the composition exhibits [certain stability/enhanced bioavailability/delivery characteristics]."

  • "A method of manufacturing the pharmaceutical composition involving [specific steps], characterized by [specific parameters]."

The scope of such claims is generally medium to narrow, depending on how broadly the chemical or procedural features are articulated.

Patent Landscape and Comparative Analysis

The patent landscape around ES2705726 features several considerations:

Prior Art and Patent Family

  • Prior Art Search: Similar patents may exist in the European patent family, especially in jurisdictions like the EPO, which seeks to protect similar innovations.
  • Overlap with Prior Art: The novelty hinges on how distinct the claimed features are relative to existing patents, such as WO patents or other EP filings.

Competitor Patents

  • Competitors may hold patents on alternative formulations or delivery systems, which could create design-around opportunities or infringement risks.
  • Patent databases, like Espacenet and DOCDB, can reveal related filings, timing (filing and priority dates), and claim overlaps.

Patent Expiry and Freedom to Operate

  • Given the priority date (assumed around 2013-2014 for a typical European patent lifecycle), expiration likely occurs around 2033-2034.
  • Freedom to operate analyses must assess the claims against existing patents, especially in key markets beyond Spain.

Patent Strategies and Trends

  • Companies often file continuation or divisional applications to extend or narrow claims strategically.
  • The emergence of second-generation patents could signal ongoing innovation efforts, affecting the patent landscape.

Legal and Regulatory Environment

  • Spanish patent law conforms to EU standards, including supplementary protection certificates (SPCs) that can extend exclusivity for medicinal products.
  • The patent’s validity can be challenged via nullity or opposition proceedings, which stakeholders should monitor.

Implications for Industry Stakeholders

ES2705726 potentially offers an enforceable barrier if the claims are sufficiently broad and well-defended. Its strategic value hinges on the scope—if narrow, competitors may develop alternative formulations; if broad, the patent could dominate a segment.

Industries should evaluate:

  • In-licensing or acquisition potential: If the patent covers a therapeutically valuable compound or platform technology.
  • R&D pathways: Whether claims can be navigated or designed around based on detailed claim language.
  • Patent enforcement: Ensuring stability against oppositions or challenges requires detailed claim and specification analysis.

Key Takeaways

  • Claim Breadth Is Crucial: The enforceability of ES2705726 depends on the language used in the claims. Broader claims offer higher protection but may attract invalidation challenges.
  • Competitive Landscape Is Dynamic: The patent family surrounding this patent must be monitored for overlapping claims, especially from competitors seeking to carve out niches.
  • Third-Party Risks and Opportunities: Narrow claims can be circumvented; broad claims offer more secure protection but require strong prior art distinctions to withstand validity challenges.
  • Lifecycle Management: Strategic use of divisional applications, supplementary protections like SPCs, and active patent monitoring enhance commercial value.
  • Market and Regulatory Context: The patent’s relevance depends on its alignment with evolving regulatory standards and market demands, emphasizing the importance of patent claims tailored to current therapeutic needs.

FAQs

  1. What is the primary competitive advantage of having a broad claim in ES2705726?
    Broad claims can protect a wide range of formulations or methods, reducing the risk of competitors designing around the patent and establishing market dominance.

  2. How does the patent landscaping surrounding ES2705726 influence licensing strategies?
    Understanding related patents helps identify potential infringement risks, licensing opportunities, and patent thickets that might inhibit entry or expansion.

  3. Can the scope of ES2705726 be challenged post-grant?
    Yes. Oppositions or nullity proceedings can be initiated in Spain or at the EPO, especially if prior art demonstrates lack of novelty or inventive step.

  4. What role do dependent claims play in strengthening the patent’s enforceability?
    They offer fallback positions and can help defend the patent by establishing specific embodiments, making infringement easier to demonstrate and invalidation more challenging.

  5. Is there a strategic advantage in filing divisional applications related to ES2705726?
    Yes. Divisional applications can refine claim scope, extend patent family coverage, or focus on narrower claims to improve validity and enforcement options.


References

  1. European Patent Office. Espacenet patent database.
  2. European Patent Office. DOCDB patent documentation.
  3. OECD. Patent Cooperation Treaty (PCT) and patent landscape reports.
  4. European Patent Convention (EPC). Laws related to patentability and enforcement.
  5. Spanish Patent Law. Relevant statutes governing patent rights and nullity procedures.

Note: Detailed claim language analysis requires access to the full patent specification and claims document for ES2705726. The overview provided reflects typical considerations for pharmaceutical patents in Spain.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.