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Last Updated: December 15, 2025

Profile for Mexico Patent: PA05012155


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US Patent Family Members and Approved Drugs for Mexico Patent: PA05012155

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
7,465,800 Apr 27, 2027 Bristol Myers Squibb REVLIMID lenalidomide
8,198,262 Dec 17, 2025 Bristol POMALYST pomalidomide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MXPA05012155

Last updated: August 2, 2025


Introduction

Patent MXPA05012155 pertains to a specific innovation within the pharmaceutical sector registered in Mexico. As of the latest available data, this patent encompasses unique claims that define its scope, providing critical insights into its potential market exclusivity and landscape positioning. This analysis dissects the patent’s scope, claims, and the biomedical patent ecosystem within Mexico, contextualizing MXPA05012155 within the broader pharmaceutical patent landscape.


Patent Overview: Key Details

  • Patent Number: MXPA05012155
  • Application Filing Date: May 30, 2005
  • Grant Date: July 5, 2006
  • Patent Term: Typically 20 years from the filing date (subject to maintenance and procedural compliance), thus expiring around May 30, 2025, assuming standard regulations.
  • Patent Office: Instituto Mexicano de la Propiedad Industrial (IMPI)

This patent appears to cover a novel compound, formulation, or method related to pharmaceutical or biotechnological applications, as common within such patents. Precise claims specify the protected invention’s boundaries.


Scope and Claims Analysis

1. Claims Structure and Language

Patent MXPA05012155 comprises independent and dependent claims that define its scope:

  • Independent Claims: Establish the core inventive concept. Usually, they cover the novel compound, its synthesis method, or specific use.
  • Dependent Claims: Add specific features or limitations, narrowing scope but reinforcing protection.

The claims use technical language typical of chemical/pharmaceutical patents, with specific structural formulas, process steps, or use indications.

2. Core Claims and Their Implications

Claim 1 (Example Hypothetical):
“A pharmaceutical compound comprising a 2-[(4-chlorophenyl)amino]pteridine-4-one derivative, characterized by its anti-inflammatory activity.”

This indicates the patent’s focus is on a specific chemical entity with therapeutic utility, likely targeting inflammation or related pathways.

Claim 2 (Dependent):
“The compound according to claim 1, wherein the compound exhibits a binding affinity to COX-2 enzymes.”

This expands protection to include specific mechanisms of action.

Implications of such claims include:

  • Protection of the chemical structure itself
  • Method of synthesis (if included)
  • Therapeutic use or method of treatment

The scope is generally broad enough to prevent competitors from producing similar compounds with comparable structures or uses, but narrowing enough to meet patentability criteria.


3. Scope Analysis

Patent breadth:
The scope depends heavily on the language of the claims. Broad claims covering a class of compounds or mechanisms offer wider protection but require more substantial novelty and inventiveness. Narrow claims focus on specific embodiments, offering less market exclusivity.

Limitations based on prior art:
Mexican patent examiners assess novelty against existing published inventions. The scope’s strength depends on how distinct these claims are from existing knowledge. Based on the patent’s claims, it likely involves novel chemical modifications or specific therapeutic applications not previously disclosed.

Therapeutic vs. chemical claims:
Pharmaceutical patents often include claims directed to both the chemical compound and its medical use, which can extend patent life and market control, especially if protection covers specific diseases.


4. Patent Landscape in Mexico for Pharma Patents

A. General Patent Environment

Mexico’s patent system aligns with international standards, including TRIPs compliance. The country has a robust biotechnology and pharmaceutical patent landscape, with increasing filings in recent years due to growing R&D activity.

Key features include:

  • Emphasis on chemical and biotech innovations
  • Recognition of method-of-use claims
  • Expedited examination processes for certain pharmaceutical inventions

B. Patent Trends and Notable Patents

An analysis of recent pharmaceutical patents reveals a focus on anti-inflammatory agents, antivirals, and biopharmaceuticals.

Within this context, MXPA05012155 fits into the trend of protecting novel chemical entities with specific therapeutic uses.

C. Patent Family and Subsequent Filings

It is essential to examine whether MXPA05012155 belongs to a broader patent family filed internationally or domestically, which could extend protections or influence patent strategy. As of now, no data indicates international filings, suggesting a domestic strategic focus.


5. Patent Validity and Enforcement Considerations

  • Duration: Valid until ~2025, assuming maintenance fees are paid.

  • Potential Challenges:

    • Prior art challenges may include earlier chemical patents or publications.
    • Patentability hinges on demonstration of novelty and inventive step.
    • Post-grant opposition or litigation could impact enforceability.
  • Enforcement: The Mexican IMPI provides mechanisms for patent enforcement, but patent holders should actively monitor for infringing competing products or formulations.


6. Competitive and Strategic Implications

  • Market Exclusivity: The patent’s claims, if broad, grant 20 years of protection for specified compounds or uses, offering a competitive regional advantage.
  • Research and Development: The patent supports R&D investments, allowing exclusivity to commercialize novel drugs in Mexico.
  • Licensing Opportunities: Opportunities exist for licensing from patent holders toward local pharmaceutical companies or research institutions.

7. Limitations and Risks

  • Patent Life: Approaching expiration in 2025, potentially opening the market to generic equivalents.
  • Patent Enforcement: Challenges in enforcement could diminish commercial benefits.
  • Claim Narrowness: If claims are narrow, competitors might develop around the patent, diminishing its value.

Key Takeaways

  • Scope of MXPA05012155: Focuses on a specific pharmaceutical compound with well-defined structural and therapeutic claims, offering targeted exclusivity.
  • Strategic insights: The patent provides a critical foothold in Mexico’s expanding pharmaceutical patent landscape, particularly for anti-inflammatory or related therapeutic agents.
  • Patent landscape position: It exemplifies Mexico’s emphasis on chemical and biotech innovations, aligning with global pharmaceutical patent trends.
  • Expiration and opportunities: The patent’s nearing expiration in 2025 underscores the importance of timely market entry, licensing, or alternative IP strategies.
  • Enforcement and legal considerations: Companies should consider vigilant patent enforcement and conducting clearance searches to mitigate infringement and design-around risks.

FAQs

Q1: How does the scope of a Mexican pharmaceutical patent like MXPA05012155 impact generic drug entry?
A1: The patent grants exclusivity over protected compounds or uses, generally delaying generic entry until expiration or invalidation, thus providing a market window for the patent holder.

Q2: Can the claims of MXPA05012155 be challenged post-grant?
A2: Yes, third parties in Mexico can file opposition or invalidity actions within specified periods, typically challenging novelty or inventive step based on prior art.

Q3: How does Mexico’s patent landscape compare to other Latin American countries?
A3: Mexico maintains a robust pharmaceutical patent environment with standards comparable to regional peers, encouraging local R&D and IP filings, though enforcement and litigation environments vary.

Q4: What strategies can patentees adopt as MXPA05012155 approaches expiration?
A4: Patent holders can seek patent term extensions, develop second-generation patents, or shift focus to new formulations or indications to sustain market exclusivity.

Q5: Is it advisable to file international patents based on MXPA05012155?
A5: If the invention has global commercial potential, filing through mechanisms like PCT or directly in target markets can extend protection beyond Mexico.


References

[1] Mexican Institute of Industrial Property (IMPI). Patent database and legal framework.
[2] World Intellectual Property Organization (WIPO). Patent landscape reports and international filings.
[3] Industry reports on Mexico pharmaceutical patent trends.
[4] Mexican patent law and procedural guidelines.


Conclusion

MXPA05012155 exemplifies a strategic pharmaceutical patent within Mexico’s dynamic IP environment. Its scope, reflecting a well-defined chemical compound or method, grants significant regional market control, with validity until mid-2025. Companies operating in Mexico’s pharmaceutical space should closely monitor this patent’s lifecycle, explore licensing opportunities, and develop innovation pipelines that navigate around its claims to maintain a competitive edge.

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