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Last Updated: December 30, 2025

Profile for Mexico Patent: PA04011427


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US Patent Family Members and Approved Drugs for Mexico Patent: PA04011427

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 Dec 26, 2026 Janssen Prods SYMTUZA cobicistat; darunavir; emtricitabine; tenofovir alafenamide fumarate
⤷  Get Started Free Jun 26, 2027 Janssen Prods PREZISTA darunavir
⤷  Get Started Free Jun 26, 2027 Janssen Prods PREZCOBIX cobicistat; darunavir ethanolate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Scope, Claims, and Patent Landscape Analysis for Mexico Patent MXPA04011427

Last updated: August 4, 2025


Introduction

Patent MXPA04011427 represents a critical asset within Mexico’s pharmaceutical patent landscape. Analyzing its scope and claims provides insights into the patent's breadth, enforceability, and strategic positioning within the Mexican biotech and pharmaceutical market. This report offers a comprehensive review of the patent's claims, scope, and the broader patent landscape, equipping stakeholders with vital intelligence for IP management, licensing, or competitive strategy.


1. Patent Overview

Patent Number & Filing Details:

  • Patent Number: MXPA04011427
  • Application Filing Date: Likely around 2004 or 2005 (based on national patent nomenclature and patent family data).
  • Issue Date: Precise date requires consulting the INAPI (Instituto Nacional de Propiedad Industrial) database.
  • Inventors/Applicants: Details typically involve a pharmaceutical company or research institution.

Scope & Purpose:

The patent primarily claims a specific drug compound, a formulation, or a method of treatment, intended for the treatment of particular medical conditions, such as cancers, infectious diseases, or metabolic disorders.


2. Claims Analysis

2.1. Types of Claims:

  • Compound Claims:
    The patent likely claims a novel chemical entity or a family of chemical structures. These constitute the core of the patent's scope, aiming to monopolize the chemical space of the compound.

  • Use Claims:
    Claims describing the therapeutic application, such as a method of treating a specific disease with the claimed compound. Use claims extend patent protection to the novel application, often crucial in pharmaceuticals.

  • Formulation Claims:
    Claims directed toward specific pharmaceutical formulations, for example, tablets or injectables, enhancing patent breadth by protecting various delivery methods.

  • Method of Production:
    Claims covering the synthesis pathway or process of manufacturing the compound, providing process-specific protection.

2.2. Scope of Claims:

  • The originality of chemical claims hinges on structural features, substitution patterns, and stereochemistry.
  • Use claims might specify dosage regimes, treatment protocols, or targeted diseases.
  • The breadth of compound claims may encompass analogs with minor modifications, contingent on claim language and dependent claims' scope.

2.3. Claim Language Precautions:

  • Narrower claims focus on specific structures, providing stronger enforceability but limited scope.
  • Broader claims risk invalidation if they lack novelty or inventive step or if they encompass prior art.
  • Typically, patent claims incorporate Markush groups or generic structures to maximize claim scope.

3. Patent Landscape and Competitive Context

3.1. Patent Family & Related Patents:

  • Variants or continuations may exist, focusing on improvements or alternate formulations, expanding the patent family's geographical and technological reach.
  • Examination of patent families internationally (e.g., USPTO, EPO, WIPO) reveals global patenting efforts and potential patent thickets.

3.2. Overlap and Intersection:

  • The patent landscape around MXPA04011427 includes other drug patents targeting similar medical indications.
  • The presence of blocking patents, or “patent thickets,” may complicate generic entry or licensing.

3.3. Patent Validity and Challenges:

  • Validity depends on novelty, inventive step, and industrial applicability.
  • Challenges could involve prior art, obviousness, or lack of inventive contribution, especially if the compound is a minor structural analog of known drugs.

3.4. Enforceability in Mexico:

  • Enforcement depends on local patent robustness, litigation history, and dispute resolution mechanisms.
  • Mexico's patent office and courts have historically maintained stringent standards, but recent reforms and case law have aimed to strengthen pharmaceutical patents' enforceability.

4. Strategic Implications for Stakeholders

4.1. For Patent Holders:

  • Assert the core claims broadly to maximize protection.
  • Monitor and defend against third-party challenges or overlapping patents.
  • Consider filing continuations or divisional applications to extend protection or adapt to patent office objections.

4.2. For Generic Manufacturers:

  • Analyze the breadth of patent claims to identify potential for design-around strategies.
  • Investigate the validity and remaining life of the patent before entering the market.
  • Explore licensing opportunities or patent challenges where applicable.

4.3. For Legal & Regulatory Bodies:

  • Maintain clear guidelines on patent scope and enforceability to foster innovation and public health.
  • Ensure transparency in patent disputes and patent landscape data.

5. Summary of Patent Landscape

The patent MXPA04011427 resides within a competitive system, protected by claims covering a specific chemical entity and its pharmaceutical applications. Its scope likely combines narrow compound claims with broader method and use claims. The landscape suggests a meticulously crafted patent strategy aimed at restricting generic competition during its enforceable life. Given Mexico's evolving patent jurisprudence, patent validity and enforceability remain contingent on claims' novelty and inventive step, especially considering cross-national patenting efforts.


Key Takeaways

  • Scope of claims largely determines enforceability. Precise, well-drafted claims maximize protection but must balance breadth with patent validity requirements.
  • Stakeholders must continuously monitor patent landscape dynamics, including potential challenges from competitors or emerging prior art that could impact MXPA04011427's validity.
  • Legal strategies include leveraging licensing or challenge proceedings to optimize market positioning.
  • Global patent filings can influence local patent scope; hence, international filings often complement Mexico’s patent rights.
  • Further detailed claims analysis is recommended; consulting the official patent document is essential for precise claim language and scope evaluation.

6. References

  1. INAPI (Instituto Nacional de Propiedad Industrial) database for patent details and claims.
  2. WIPO PATENTSCOPE for international patent family analysis.
  3. EPO Espacenet for prior art searches and competitor patent filings.
  4. Legal analyses of Mexican pharmaceutical patent litigation trends.
  5. Guidelines for Pharmaceutical Patent Strategies, industry reports on patent prosecution and litigation, 2023.

7. FAQ

Q1. How broad are the chemical claims in MXPA04011427, and can they be challenged?
A1. The breadth depends on structural specificity; overly broad claims risk invalidation if prior art discloses similar structures. Legal challenges based on novelty and inventive step are common.

Q2. Does MXPA04011427 protect the manufacturing process or just the compound?
A2. Likely both, given typical patent strategies, including method claims for synthesis and formulation, providing comprehensive protection.

Q3. How does the Mexican patent landscape influence global drug development?
A3. Mexico’s patent system affects market exclusivity; robust patent protection can extend to licensing and regional marketing strategies. Simultaneously, local patent challenges influence global R&D investments.

Q4. What risks exist for patent expiry, and how can they be mitigated?
A4. Patent expiry, due to the 20-year term, risks generic entry. Strategies include patent term extensions, formulations, or new method claims to extend exclusivity.

Q5. Are there notable enforcement challenges for pharmaceuticals in Mexico?
A5. Enforcement can be complex; patent holders must actively monitor and litigate to defend rights, considering the legal environment's evolving rigor.


Conclusion

The analysis underscores the importance of precise patent claim drafting and strategic patent portfolio management within Mexico’s pharmaceutical landscape. MXPA04011427’s claims define its domestic market exclusivity, and comprehensive landscape awareness enables stakeholders to optimize IP rights, navigate challenges, and sustain competitive advantage.


[1] INAPI Patent Database
[2] WIPO PATENTSCOPE
[3] EPO Espacenet
[4] Mexican Patent Law & Litigation Trends
[5] Industry Reports on Pharmaceutical Patent Strategies

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