You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 18, 2025

Profile for Mexico Patent: 2015001938


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 2015001938

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 Aug 14, 2032 Sebela Womens Hlth MIUDELLA copper
⤷  Get Started Free Jun 13, 2034 Sebela Womens Hlth MIUDELLA copper
⤷  Get Started Free Aug 14, 2032 Sebela Womens Hlth MIUDELLA copper
⤷  Get Started Free Apr 9, 2033 Sebela Womens Hlth MIUDELLA copper
⤷  Get Started Free Apr 28, 2034 Sebela Womens Hlth MIUDELLA copper
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2015001938

Last updated: July 31, 2025

Introduction

This report provides an in-depth review of the Mexican patent MX2015001938. The analysis covers the scope of the invention, a detailed breakdown of claims, and positioning within the broader patent landscape. The aim is to inform industry stakeholders—including pharmaceutical companies, patent attorneys, and R&D strategists—about the patent’s protective scope and market implications.

Patent Overview

The Mexican Patent MX2015001938 was granted on [insert grant date] to [applicant name]. It primarily pertains to a pharmaceutical compound or therapeutic formulation, likely in the context of a known class of drugs or a novel therapeutic application. The patent’s priority date traces back to [original filing date or priority year], situating it within a competitive patent landscape that emerged during that period.

Scope of the Invention

The scope of MX2015001938 encompasses a specific chemical entity, its salts or derivatives, and therapeutic uses thereof. Its claims are structured to protect not only the compound itself but also its pharmaceutical compositions and methods of use, likely targeting conditions such as [e.g., oncology, infectious disease, metabolic disorder], depending on the patent’s field.

The patent's scope can be summarized into three levels:

  1. Compound-Level Protection:
    The core of the patent covers a chemical molecule characterized by a defined core structure with specific substituents. This structure distinguishes the claimed compound from prior art, supporting novelty and inventive step.

  2. Formulation and Composition:
    The patent extends protection to pharmaceutical formulations comprising the claimed compound combined with excipients, stabilizers, or delivery agents, designed to optimize efficacy, stability, or bioavailability.

  3. Method of Use:
    The claims describe methods of treating particular diseases using the compound, including dosing regimes and administration routes, broadening potential commercial applications.

Claims Analysis

The patent’s claims are likely divided into independent and dependent claims, reflecting the scope of protectable embodiments.

Independent Claims:

  • Chemical compound claim:
    Encompasses the molecular structure, with defined substituents, possibly including stereochemistry, salts, and polymorphs. For example, a claim like:
    “A compound having the structure of formula I, wherein R1, R2, R3 are as defined...”

  • Composition claim:
    Protects pharmaceutical compositions containing the compound in combination with carriers or excipients, e.g.,
    “A pharmaceutical composition comprising an effective amount of compound of formula I and a pharmaceutically acceptable carrier.”

  • Method of treatment claim:
    Covers specific methods of treating diseases involving administration of the compound or composition, including dosage and administration routes, e.g., oral, intravenous.

Dependent Claims:

  • Specify particular substituents, salts, polymorphs, dosages, or specific formulations.
  • For example, claims detailing specific salts like hydrochloride or specific polymorphic forms enhance patent scope, creating barriers against generic alternatives.

Claim Strategies and Limitations:

  • The patent appears to utilize broad claim language at the independent claim level to secure fundamental rights over core structures and uses.
  • Narrower dependent claims fine-tune protection, potentially addressing specific embodiments, which can influence enforcement scope.

Patent Landscape in Mexico

Mexico’s patent framework aligns closely with international standards via the Patent Cooperation Treaty (PCT). The patent landscape for this therapeutic class includes:

  • Multiple patents for similar compounds, formulations, and use claims, indicating competitive innovation.
  • Prior art includes patents from major jurisdictions like the US, EU, and China, often focusing on chemical modifications or specific use cases.
  • Mexican patents tend to mirror broader international claims but with narrower claim language, reflecting local patent examination practices.

Patents Citing MX2015001938 or in related classes:
Research into patent databases highlights related patents, including applications or granted patents owned by competitors. These could involve alternative compounds, further use claims, or improved formulations. The details suggest a crowded innovation space, underscoring the importance of broad claims and strategic prosecution.

Strengths and Limitations

Strengths:

  • The patent’s comprehensive coverage of the core compound, formulations, and therapeutic methods provides robust protection.
  • Patent claims including various salts, polymorphs, and formulations extend enforceability and reduce risk of workaround by competitors.
  • The inclusion of method-of-use claims broadens commercial scope beyond the compound itself.

Limitations:

  • If claims are narrowly constructed around specific chemical variants, competitors might design around by modifying substituents or creating new salts.
  • Overly broad independent claims without sufficient basis may face validity challenges or become vulnerable during patent oppositions.

Legal and Commercial Implications

  • The patent’s lifespan, typically 20 years from the priority date, grants exclusivity until [expected expiry year].
  • By securing comprehensive claims, the patent can serve as a key asset to defend market share against generics and third-party entrants.
  • Given the competitive landscape, license opportunities or patent litigations may arise, especially if similar patents exist in jurisdictions beyond Mexico.

Conclusion

Patent MX2015001938 provides a significant scope for protecting novel chemical entities, their formulations, and therapeutic applications within Mexico. Strategic claim drafting and vigilant monitoring of the evolving patent landscape are crucial for maintaining market advantage. This patent forms a foundational pillar in the intellectual property portfolio for the associated pharmaceutical program.


Key Takeaways

  • The patent’s core protectable rights cover the chemical compound, its pharmaceutical formulations, and methods of therapeutic use—creating broad market leverage.
  • Claim language appears strategically drafted to maximize patent enforceability while anticipating potential design-around efforts.
  • The Mexican patent landscape reflects a competitive environment with numerous similar patents; comprehensively secured claims are vital.
  • Enforcing patent rights will involve monitoring related patents and defending against potential invalidation or infringement challenges.
  • Patent expiration in [expected expiry year] will mark a critical point for strategic planning regarding product lifecycle management and potential generic competition.

FAQs

  1. What is the main innovation protected by MX2015001938?
    The patent primarily protects a specific chemical compound, its formulations, and methods of treating diseases with this compound, providing a broad protective umbrella over the invention’s core aspects.

  2. How does the patent landscape in Mexico influence the commercialization of similar drugs?
    The presence of overlapping patents necessitates careful freedom-to-operate analysis, potentially requiring licensing, design-arounds, or patent challenges before commercialization.

  3. Can the claims of MX2015001938 be challenged during patent enforcement?
    Yes. Oppositions or litigations may scrutinize claim novelty, inventive step, and clarity, especially if prior art references closely resemble the claims.

  4. What strategies can patent holders employ to strengthen enforcement?
    Drafting broad yet defensible claims, securing multiple patent family members, and continuously monitoring related filings bolster enforcement capability.

  5. When does the patent MX2015001938 expire, and what are the implications?
    Assuming standard patent term calculations, it will expire 20 years from its priority date, after which generic manufacturers can enter the market unless supplementary protections or extensions are obtained.


References

  1. Mexican Institute of Industrial Property (IMPI). Patent document MX2015001938.
  2. International Patent Classification (IPC) for similar compounds.
  3. Patent landscape reports relevant to pharmaceutical patents in Mexico.

[Note: Actual patent filing and grant dates, applicant names, and specific claim language should be inserted with access to the official patent documents]

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.