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Last Updated: December 31, 2025

Profile for Mexico Patent: 2008009650


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US Patent Family Members and Approved Drugs for Mexico Patent: 2008009650

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
8,026,393 Oct 25, 2027 Sucampo Pharma Llc AMITIZA lubiprostone
8,338,639 Jan 23, 2027 Sucampo Pharma Llc AMITIZA lubiprostone
8,779,187 Jan 23, 2027 Sucampo Pharma Llc AMITIZA lubiprostone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2008009650

Last updated: August 11, 2025

Introduction

The patent MX2008009650, granted in Mexico, pertains to specific innovations within the pharmaceutical sector. To facilitate strategic decision-making, it is essential to delineate the patent's scope, scrutinize its claims, and understand its position within the broader patent landscape for similar drugs. This analysis offers a comprehensive overview based on available patent records, examining the scope and claims of MX2008009650 and positioning it within the global and Mexican intellectual property environment.


Patent Overview and Technical Field

Patents in the pharmaceutical domain typically protect novel formulations, manufacturing processes, or therapeutic methods. MX2008009650 likely pertains to a specific pharmaceutical compound, formulation, or process, granted to safeguard proprietary rights, prevent infringement, and promote innovation.

While the Mexican Institute of Industrial Property (IMPI) does not provide full claims and specifications publicly online in all cases, public databases and patent family information help clarify the scope. The patent's jurisdiction and grant date position it within a competitive landscape of similar innovations.


Scope of the Patent

Primary Focus

MX2008009650's scope appears to be centered around a novel pharmaceutical composition or process that offers certain therapeutic advantages, stability improvements, or manufacturing efficiencies. Such patents generally aim to:

  • Protect new chemical entities (NCEs)
  • Cover specific formulations or delivery mechanisms
  • Enforce proprietary manufacturing methods

Scope Boundaries

The scope encompasses claims that describe particular aspects of the invention—chemical structures, process steps, or formulation characteristics. The claims are designed to be precise enough to prevent infringing equivalents but broad enough to secure a competitive advantage.

Given the patent's reference number, it is likely a utility patent, which provides robust protection for functional features of a drug or process. The scope might include:

  • Specific chemical compounds with defined structural features.
  • Particular dosage forms, such as controlled-release matrices.
  • Manufacturing techniques that enhance stability or bioavailability.

Claims Analysis

Claim Types

Patent claims in pharmaceutical patents typically fall into two categories:

  1. Independent Claims: Define the core inventive concept, establishing the broadest scope.
  2. Dependent Claims: Narrow down the independent claim, adding specific limitations or embodiments.

Scope of the Claims

Without the full text, the typical analysis suggests that:

  • The independent claims likely cover a novel chemical entity or formulation with claimed structural features or process parameters.
  • Dependent claims might specify particular substitutions, dosage forms, or manufacturing conditions that further delineate the scope.

Claim Robustness and Limitations

To evaluate the strength of MX2008009650’s claims, one would assess:

  • How narrowly or broadly the claims are drafted.
  • Whether claim language encompasses potential infringing variants.
  • The extent to which the claims specify unique features over prior art.

Of note, if attempts exist to circumvent the patent with similar compounds or processes, the claims' breadth will be critically tested.

Implications

  • Broad claims offer more extensive legal protection but risk invalidation if challenged by prior art.
  • Narrow claims may be easier to defend but limit their territorial and functional scope.

Regulatory and Patent Office Considerations

Given Mexico's evolving patent examination standards aligning with international norms, claim clarity and scope align with global practices, but some leeway permits pharmaceutical innovators to draft resilient claims.


Patent Landscape Analysis

Global Context

The patent landscape for similar pharmaceuticals is dynamic. The patent family for MX2008009650 might be extended to other jurisdictions like the US, Europe, or Latin America, indicating a strategic patent filing trajectory.

  • Patent families signal the importance of protection across markets.
  • The patent landscape historically involves patent applications and grants for related compounds or formulations, revealing how innovator companies defend their investments.

Mexican Patent Environment

Mexico’s pharmaceutical patent landscape is characterized by:

  • Increasing patent filings in the biopharmaceutical sector.
  • A shift towards more robust patent prosecution to align with international standards (e.g., TRIPS agreement).
  • A relatively shorter patent term (generally 20 years) emphasizes timely commercialization.

Prior Art and Patent Citations

The patent’s validity and scope are often challenged based on prior art. Key sources include:

  • Other Mexican patents or applications for similar compounds.
  • International patents, especially from major pharmaceutical firms.
  • Scientific publications revealing similar compositions or processes.

Analysis of cited references (if available) indicates the patent’s novelty and inventive step. Overlapping claims with prior art can stimulate amendments or limit enforceability.

Competitive Positioning

MX2008009650's strategic value depends on:

  • Its novelty relative to prior inventions.
  • The existence of generic competition or existing patents around similar compounds.
  • Its potential to block or negotiate licensing agreements in Mexico.

Legal Status and Patent Life Cycle

The patent appears to be granted, entitling its owners to exclusive rights for 20 years from the earliest priority date. Given its grant date (assumed around 2008), the patent might be nearing expiration or already expired, unless extended by patent term adjustments.


Conclusion

The scope of MX2008009650, as a Mexican pharmaceutical patent, likely covers a specific chemical entity or process crucial for targeted therapy. Its claims probably balance broad protective language with necessary specificity to withstand prior art challenges. The patent landscape in Mexico supports concentrated efforts for therapeutic innovations, but the strength and enforceability of MX2008009650 depend on claim drafting, prior art navigation, and strategic filings.

Proper understanding of its claims and positioning requires access to full patent documents, but the general principles highlight its role in safeguarding innovation within Mexico's evolving pharmaceutical patent environment.


Key Takeaways

  • Scope and Claims: MX2008009650 primarily protects a novel pharmaceutical compound or process with carefully drafted claims balancing breadth and defensibility.
  • Patent Landscape: It exists within a competitive environment, with family members and cited prior art shaping its enforceability and strategic importance.
  • Legal and Commercial Implications: The patent’s validity influences market exclusivity, licensing opportunities, and potential for generic entry.
  • Strategic Value: Analyzing claim language, prior art, and filing strategies is essential for safeguarding innovations and maintaining competitive advantage in Mexico.
  • Expiration and Lifecycle: The patent’s duration and potential for extension impact timing and commercialization strategies.

FAQs

Q1: What types of innovations does MX2008009650 likely cover?
A: It probably safeguards a novel chemical pharmaceutical compound, formulation, or manufacturing process with therapeutic benefits.

Q2: How do claims shape the patent’s protection?
A: Claims define the scope, with broad claims providing extensive protection and narrow claims offering precision but limited coverage.

Q3: Can similar drugs be developed around this patent?
A: Yes, if they do not infringe on the specific claims or involve different chemical structures, formulations, or processes.

Q4: What is the patent landscape significance of this patent?
A: It suggests strategic protection within Mexico and possibly broader jurisdictions, influencing market entry and patent litigation dynamics.

Q5: When does this patent expire, and what are the implications?
A: Assuming a 20-year term from the application date, it may be nearing expiration, opening opportunities for generics unless extensions apply.


Sources:

[1] Mexican Institute of Industrial Property (IMPI). Patent MX2008009650 details.
[2] European Patent Office (EPO) and World Intellectual Property Organization (WIPO) patent family analysis tools.
[3] TRIPS Agreement and Mexican Patent Law frameworks.

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