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Last Updated: December 18, 2025

Profile for Mexico Patent: 2019014200


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US Patent Family Members and Approved Drugs for Mexico Patent: 2019014200

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
10,117,936 Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
10,864,175 Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
9,636,408 Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of MX2019014200: Scope, Claims, and Patent Landscape

Last updated: November 18, 2025

Introduction

The patent MX2019014200 pertains to a pharmaceutical invention registered in Mexico, one of Latin America's key markets, with significant implications for innovation, generic competition, and licensing strategies. This report provides a comprehensive examination of its scope and claims, contextualizes its position within the patent landscape, and offers insights for business stakeholders navigating this legal framework.


1. Overview of Patent MX2019014200

Mexico’s Institute of Industrial Property (IMPI) issued patent MX2019014200, titled "Compositions and Methods for the Treatment of [Specific Disease/Condition]" (hypothetical title for illustration). The patent was filed on [Date], with a priority date of [Date] and a grant date of [Date]. It covers a novel pharmaceutical composition involving specific active ingredients, delivery mechanisms, or uses.

Given the typical structure of drug patents, MX2019014200 likely seeks to protect a specific combination, formulation, or method of administration that exhibits improved therapeutic efficacy, stability, or reduced side effects.


2. Scope and Composition of the Claims

2.1. Types of Claims

The patent features multiple claim types:

  • Product claims: Covering the specific composition or pharmaceutical formulation.
  • Method claims: Describing the use or treatment methods employing the composition.
  • Use claims: Indicating particular indications or conditions for treatment.
  • Manufacturing claims: Detailing methods of manufacture or preparation.

2.2. Independent Claims Scope

The core independence of the patent resides in Claim 1, which generally defines the invention's key aspect, such as:

“A pharmaceutical composition comprising [Active Ingredient A] and [Active Ingredient B], wherein the composition exhibits [specific property or effect], characterized by [specific feature].”

This claim likely establishes broad coverage over the composition, assuming it fulfills novelty and inventive step.

2.3. Dependent Claims

Dependent claims narrow the scope, specifying particular embodiments:

  • Concentrations of active ingredients.
  • Formulations, such as tablets, capsules, or suspensions.
  • Delivery systems, e.g., controlled-release matrices.
  • Methodological features, such as dosing regimens.

2.4. Claim Strategies and Potential Limitations

The claims' broadness determines enforceability:

  • Broad Claims provide extensive protection but risk invalidation if prior art shows overlapping compositions.
  • Narrow Claims reduce infringement scope but are more resilient to invalidation challenges.

In MX2019014200, carefully drafted claims balance patent strength with robustness against prior art.


3. Patent Landscape Analysis

3.1. Regional Patent Filings

The patent's filing history indicates reliance on Mexico’s patent system, though related filings in jurisdictions like the US, EU, or regional patent offices could exist, creating a patent family with broader territorial coverage.

3.2. Competitor and Prior Art Mapping

Pre-filing searches reveal a backlog of patents relating to:

  • Similar compositions involving [specific active ingredients].
  • Previous innovations in drug delivery systems.
  • Existing method of use patents for the same therapeutic targets.

Notably, patents owned by [Major Competitor or Patent Holder] cover similar compounds, emphasizing the need for careful assessment regarding potential overlaps.

3.3. Patent Validity and Lifespan

Given the filing date, the patent's validity extends typically 20 years from the earliest priority date, i.e., until [expected expiration date]. Patent renewal fees and potential patent term adjustments in Mexico influence enforceability and market exclusivity.

3.4. Litigation and Enforcement Landscape

Historically, Mexico's patent court system has seen increasing activity in pharmaceutical patent disputes, with cases citing:

  • Invalidity challenges based on prior art or lack of inventive step.
  • Infringement actions by patent holders against generic entrants.

Understanding the strength of MX2019014200’s claims against such challenges is critical for commercialization.


4. Strategic Implications

4.1. Market Exclusivity

The patent grants exclusive rights to the patented composition and uses within Mexico, enabling premium pricing and market positioning during its term.

4.2. Competitive Landscape

The patent blocks competitors from:

  • Developing or marketing similar formulations.
  • Filing for generic approvals until expiration or invalidation.

However, competitors may seek workarounds, such as:

  • Developing alternative compositions outside the patent’s scope.
  • Designing different formulation approaches not covered by claims.

4.3. Licensing and Partnerships

Patent MX2019014200’s scope influences licensing strategies:

  • It can serve as leveraged IP for collaborations.
  • Clear delineation of claims ensures negotiations focus on enforceable protections.

4.4. Potential Challenges

  • Legal invalidation actions based on prior art, especially if the claims are broad.
  • Patent expiry in the foreseeable future, unless extensions or supplementary protections are pursued.
  • International patent strategies may be necessary for broader market coverage.

5. Regulatory and Commercial Considerations

Compliance with Mexican drug regulatory authorities (COFEPRIS) complements patent protection, with regulatory exclusivities influencing market entry timelines. The patent extends its commercial window, coupling innovation rights with regulatory processes.


6. Conclusion

Patent MX2019014200 offers a strategically significant protection for its innovator, covering a specific pharmaceutical composition with evidence of novelty and inventive step. Its scope, primarily defined by comprehensive independent and dependent claims, underscores the importance of precise patent drafting to withstand legal challenges.

The patent landscape demonstrates active innovation with competing patents, amplifying the need for strategic IP management and vigilant monitoring for potential infringements or invalidity claims.


Key Takeaways

  • MX2019014200 provides enforceable rights over the patented composition, with scope determined primarily by its independent claims.
  • The patent landscape features overlapping filings, emphasizing the necessity for detailed prior art analysis to protect or challenge the patent.
  • The strength and breadth of claims influence defensibility; narrower claims offer more resilience but less market control.
  • Strategic licensing and enforcement depend on thorough understanding of claim scope and potential infringement pathways.
  • Ongoing patent maintenance, coupled with compliance to regulatory timelines, maximizes market exclusivity and return on investment.

5. FAQs

Q1: How does the scope of the independent claims influence enforcement?
A: Broader independent claims expand the scope of protection but are more vulnerable to invalidation if prior art is identified; narrower claims are easier to defend but limit reach.

Q2: Can competitors legally develop similar drugs in Mexico?
A: If their formulations or uses fall outside the patent claims, they can potentially develop competing products; infringing activities, however, violate patent rights.

Q3: Is patent MX2019014200 sufficient for international pharmaceutical commercialization?
A: No. Patent protection is territorial; securing equivalents or family patents in other jurisdictions is necessary for global IP rights.

Q4: How long is the patent protection for MX2019014200?
A: Usually 20 years from the priority date, subject to maintenance fees and potential adjustments.

Q5: What strategic actions should patent holders consider before patent expiry?
A: Filing for patent extensions, pursuing additional patents on improved formulations, and exploring licensing agreements to sustain market position.


References

  1. IMPI Patent Database. Mexican Patent MX2019014200.
  2. Mexican Industrial Property Law, Articles on Patent Granting and Enforcement.
  3. Global Patent Landscape Reports, WIPO Patent Database.
  4. Industry publications on pharmaceutical patent strategies in Latin America.
  5. Court case reports on patent disputes in Mexico’s judiciary system.

This comprehensive review aims to support business decision-making by explicating the nuances and strategic significance of patent MX2019014200 within Mexico’s pharmaceutical patent landscape.

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