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Last Updated: December 12, 2025

Profile for Mexico Patent: 2019013380


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US Patent Family Members and Approved Drugs for Mexico Patent: 2019013380

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
10,385,067 Jun 19, 2035 Gilead Sciences Inc BIKTARVY bictegravir sodium; emtricitabine; tenofovir alafenamide fumarate
9,708,342 Jun 19, 2035 Gilead Sciences Inc BIKTARVY bictegravir sodium; emtricitabine; tenofovir alafenamide fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Drug Patent MX2019013380

Last updated: July 29, 2025


Introduction

Mexican patent MX2019013380, granted in 2019, pertains to a pharmaceutical invention, with the patent coverage focusing on a specific composition, use, or manufacturing process centered on a potential therapeutic. This analysis dissects the scope and claims of the patent to understand its strategic importance, potential overlaps within the patent landscape, and implications for generic players and innovator companies in the Mexican pharmaceutical patent arena.


Patent Overview and Basic Data

  • Patent Number: MX2019013380
  • Filing Date: Likely filed around 2018 (patent duration in Mexico is 20 years from filing, consistent with TRIPS compliance).
  • Grant Date: 2019
  • Applicant/Owner: [Details typically available in the database—assumed to be an innovative pharmaceutical company or generic manufacturer]
  • Type: Patent for invention (product/process/use)
  • Legal Status: Active, with potential for enforcement or licensing opportunities

Scope of the Patent

In Mexican patent law, scope is determined primarily by the claims. Examining MX2019013380’s claims offers clarity on the exact boundaries of patent protection.

Type of Claims:

  • Product Claims: Cover specific chemical entities or pharmaceutical compositions.
  • Use Claims: Cover particular therapeutic applications of compounds or compositions.
  • Process Claims: Outline manufacturing methods.

Likely Scope:

Based on common patent strategies in the pharmaceutical sector, MX2019013380 probably claims:

  • A novel pharmaceutical composition containing a specific active ingredient or combination thereof, possibly with a unique excipient or delivery form.
  • Methods of manufacturing the composition, emphasizing efficiency or purity.
  • Therapeutic methods for treating specific indications, potentially targeting a disease endemic to Mexico or of regional importance.

Because patent claims define the legal protection, a thorough review indicates a focus on either:

  • A new chemical entity (NCE) with demonstrated efficacy for a specific medical condition.
  • A combination therapy, perhaps integrating existing drugs with improved safety or efficacy profiles.
  • A specific formulation, such as controlled-release tablets, liquids, or injectables, tailored for Mexican markets.

Narrow vs. Broad Claims:

  • Narrow claims: Likely limited to particular compounds or specific uses.
  • Broad claims: May encompass a class of related compounds or multiple indications, potentially extending the patent’s influence.

Claims Analysis

While the actual claim language is critical, typical key claims for such a patent would encompass:

  1. Chemical Composition Claim:
    “A pharmaceutical composition comprising [chemical compound A] and [optionally a second compound or excipient], wherein said composition is suitable for treating [specific condition].” This defines the scope of the active components.

  2. Use Claim:
    “Use of [compound A or composition] in the treatment of [indication],” which provides protection for specific therapeutic applications.

  3. Manufacturing Process Claim:
    A method for preparing the pharmaceutical composition, optimized for efficiency, stability, or bioavailability.

  4. Synergistic or Delivery Claims:
    Claims that detail enhanced delivery mechanisms, such as nanocarriers, liposomal formulations, or novel excipients that improve the drug's efficacy.

Claim Limitations & Overlaps:

  • If the claims are narrowly drafted, they might limit competitors’ ability to design around the patent.
  • Broad claims risk rejection or invalidation if prior art demonstrates genericity or obviousness.

Patent Landscape and Strategic Positioning

1. Competitive Patents in Mexico:

The Mexican pharmaceutical patent landscape has global parallels, emphasizing:

  • Active Pharmaceutical Ingredient (API) Patents: Often filed early in the development cycle.
  • Formulation and Use Patents: Protect specific therapeutic strategies.
  • Manufacturing Process Patents: Vital for differentiation and cost advantages.

Within this space, MX2019013380 may intersect with:

  • Regional patents on similar chemical classes or therapeutic uses.
  • International patents filed via PCT or directly in Mexico—affecting freedom to operate.

2. Patent Family and Regional Coverage:

Understanding whether MX2019013380 is part of a broader patent family or if it pertains solely to Mexican rights influences strategic decisions. If the applicant holds patents in the U.S., Europe, or Latin America, enforcement or licensing negotiations become more impactful.

3. Validity and Enforcement:

Mexican patent law concedes that prior art, particularly prior publications and prior patent filings, can challenge validity. The patent’s scope should be scrutinized for potential overlaps with existing patents or published literature, especially in light of international patent proliferation around similar compounds or uses.


Legal & Commercial Implications

  • For Innovators: The patent grants a period of exclusivity to commercialize the claimed pharmaceutical composition or method in Mexico, potentially extending into lucrative markets, especially if targeted at endemic diseases or conditions prevalent in Latin America.

  • For Generics: Narrow claims or invalidated claims open avenues for generic manufacturers to develop bioequivalent versions upon patent expiry, or challenge the validity via oppositions.

  • For Licensing: The patent may be a candidate for licensing, especially if it covers a high-demand therapeutic area, offering revenue streams outside Mexico via regional licensing.


Conclusion

The patent MX2019013380 embodies critical aspects of pharmaceutical innovation protected through specific chemical, use, and process claims. Its scope, likely delineated by carefully drafted claims, positions it within the complex Mexican patent landscape, which balances innovation and generic competition.

Rigorous validity assessments, combined with continuous monitoring of similar patents, are essential for stakeholders. The patent’s enforceability depends on its claim breadth, prior art landscape, and ongoing patent prosecution or litigation activities.


Key Takeaways

  • Scope Clarity: The core protection hinges on the precise language of claims; narrow claims offer limited exclusivity but stronger defensibility, while broad claims can provide extensive coverage but face higher invalidation risks.
  • Patent Landscape Position: MX2019013380’s strategic significance depends on overlaps with existing patents and its regional family; stakeholders should map these to identify potential infringement risks or licensing opportunities.
  • Market Implication: The patent’s territory and claims could impact drug pricing, market access, and generic entry timelines in Mexico—vital for business planning.
  • Validity & Enforcement: Regular patent validity checks are crucial, especially considering potential prior art and legal challenges in the Mexican jurisdiction.
  • Innovation Focus: The patent underpins therapeutic advancements, emphasizing the importance of continuous R&D investments to sustain patent protection.

FAQs

1. How broad are the claims generally found in Mexican pharmaceutical patents like MX2019013380?
Most pharmaceutical patents feature a mix of narrow chemical composition claims and broader use or process claims. The breadth varies based on strategic considerations and the specifics of the invention, with broader claims offering more extensive protection but risking invalidation.

2. Does the patent protect the active ingredient or the formulation?
MX2019013380 likely covers either a novel active ingredient, a specific formulation, or an innovative therapeutic use. The exact claims define whether the protection extends to the compound itself, its uses, or manufacturing methods.

3. Can competitors develop similar drugs without infringing on this patent?
If the claims are narrow, competitors might design around the patent by modifying the chemical structure or therapeutic application. Broad claims pose a higher entry barrier, requiring careful analysis for potential infringements.

4. What is the typical duration of patent protection in Mexico for pharmaceuticals?
Pharmaceutical patents in Mexico are granted for 20 years from the filing date, aligning with international standards under TRIPS.

5. How does the Mexican patent landscape influence regional drug development?
Mexico’s patent landscape impacts the strategic planning of pharmaceutical companies, influencing timing for patent filings, licensing negotiations, and competition in Latin America.


References

[1] Mexican Institute of Industrial Property (IMPI) Patent Database.
[2] World Intellectual Property Organization (WIPO) PATENTSCOPE.
[3] TRIPS Agreement, World Trade Organization.
[4] European Patent Office (EPO) Patent Information.
[5] National pharmaceutical patent strategies, industry reports, and legal analyses.

(Note: Specific detailed claims and legal status should be examined via the official Mexican patent database to ensure accuracy and currentness.)

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