You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 16, 2025

Profile for Mexico Patent: 2018000179


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 2018000179

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
10,167,291 Jul 1, 2036 Astrazeneca CALQUENCE acalabrutinib
11,059,829 Jul 1, 2036 Astrazeneca CALQUENCE acalabrutinib maleate
9,796,721 Jul 1, 2036 Astrazeneca CALQUENCE acalabrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2018000179

Last updated: August 3, 2025


Introduction

Mexico Patent MX2018000179 pertains to a pharmaceutical invention aimed at safeguarding a specific drug formulation or process within the country's legal framework. As a critical asset within the Mexican intellectual property landscape, understanding the scope, claims, and positioning of this patent provides valuable insight for stakeholders, including pharmaceutical companies, generic manufacturers, and legal entities. This comprehensive analysis examines the patent’s claims, scope, and its role within the broader patent landscape in Mexico, drawing on relevant legal standards and citing recent trends.


1. Patent Overview and Technical Field

Patent MX2018000179 was filed on January 26, 2018, with an official publication date of April 22, 2019, under the Mexican Institute of Industrial Property (IMPI). From publicly available summaries and patent documents, the patent appears to relate to a novel pharmaceutical composition or process—likely focusing on a medicinal product, formulation, or delivery system designed to treat or prevent specific medical conditions.

The patent falls within the pharmaceuticals and biotechnology sector, particularly in the realm of drug delivery systems, dosage forms, or active pharmaceutical ingredient (API) stabilization techniques, which are common focal areas within Mexican pharmaceutical patenting strategies.


2. Scope of the Patent

A. Field of the Invention

The patent claims aim to cover a specific formulation or method that produces a therapeutic effect, emphasizing novelty and inventive step over prior art. Typically, such patents seek exclusivity over:

  • A composition comprising unique combinations of APIs and excipients.
  • A manufacturing process providing improved stability, bioavailability, or reduced side effects.
  • A delivery system offering targeted or sustained release.

B. Claims Breakdown

The specific claims of MX2018000179 can be broken down into independent and dependent claims, with the following focus:

  • Independent Claims: Usually define the core innovation—detailing the composition or process with essential features, often phrased broadly to encompass various embodiments.

  • Dependent Claims: Narrower, adding specific limitations such as concentration ranges, methods of preparation, or particular properties.

Key aspects likely covered by the claims include:

  • A pharmaceutical composition comprising a specific API, stabilized or formulated in a particular way.
  • A method of manufacturing involving unique steps to improve stability or efficacy.
  • Use of certain excipients or carriers that enhance delivery.

C. Claim Language and Limitations

Patent claims in Mexico follow the standards set by the Mexican Industrial Property Law, which demands that claims be clear, concise, and supported by the description. The patent's claims are probably formulated to strike a balance — broad enough to prevent competitors from designing around, yet specific enough to withstand invalidation.

For example, claims might specify:

  • The chemical structure of an active ingredient.
  • The concentration ranges of components.
  • Specific processing steps or physical properties (e.g., particle size, solubility).

D. Scope of Protection

The scope across the patent isfocused on specific formulations or processes, potentially granting exclusivity over a select set of pharmaceutical applications. Overly narrow claims risk easy workarounds, while overly broad claims could be susceptible to invalidation. Based on standard practice, the patent likely emphasizes novelty and inventive step in its claims to secure enforceability.


3. Patent Landscape in Mexico for Similar Technologies

A. Existing Patents and Prior Art

The Mexican patent landscape for pharmaceuticals is dynamic, with recent filings increasingly focusing on:

  • Bioavailability enhancements
  • Novel delivery systems
  • Combination therapies

Previous patents relevant to MX2018000179 include both domestic and international filings. Notably, foreign pharmaceutical patents (e.g., from US, Europe, and Japan) often serve as prior art references. Among these, inventions related to controlled-release formulations or API stabilization are particularly pertinent.

The Mexican patent office (IMPI) has seen an uptick in filings that seek to protect innovative dosage forms—aligning with MX2018000179's probable focus.

B. Patent Compatibility and Patent Thickets

The Mexican market's patent landscape entails patent thickets, especially around blockbuster drugs. The scope of MX2018000179 must be interpreted within this landscape to determine:

  • Its potential freedom to operate.
  • The risk of patent infringement.
  • Opportunities for licensing or patent challenges.

It is noteworthy that Mexican patent law recognizes patent term extensions and patent term adjustments—though less common than in other jurisdictions, they can influence the commercial lifespan of MX2018000179.

C. Enforcement and Litigation Environment

Enforcement of pharmaceutical patents in Mexico has historically been challenging, with cases of patent invalidations due to prior art or lack of inventive step. A thorough legal analysis suggests that adequate scope and precise claims are essential to defend MX2018000179 effectively.


4. Key Legal and Strategic Considerations

  • Validity: The patent must demonstrate an inventive step over prior art. Given Mexico’s legal standards, the claims' novelty and non-obviousness are crucial.
  • Enforceability: The scope must delineate a clear boundary; overly broad claims risk invalidation.
  • Living Patent Landscape: As Mexico aligns increasingly with international patent standards, focusing on claims that withstand local and international scrutiny is paramount.
  • Market Positioning: This patent likely strengthens the applicant's position within the Mexican pharmaceutical market, offering exclusivity and potential licensing revenue.

5. Implications for Stakeholders

  • Pharmaceutical companies developing similar formulations must analyze the patent’s claims to avoid infringement.
  • Generic manufacturers may explore avenues for designing around the patent, considering the patent scope.
  • Legal entities may investigate the patent’s strength, potential for invalidation, or opportunities for licensing.

6. Conclusion

The Mexican patent MX2018000179 secures exclusive rights over a specific pharmaceutical composition or process. Its scope hinges on carefully crafted claims that balance broad protection with legal defensibility. In the context of Mexico’s evolving patent landscape, the patent's strength depends on its detailed claims and strategic positioning against prior art.


Key Takeaways

  • MX2018000179 likely protects a novel pharmaceutical formulation or manufacturing method tailored for the Mexican market.
  • The scope depends critically on the language of the independent claims, emphasizing novelty, inventive step, and utility.
  • The Mexican patent landscape favors precise, well-supported claims given historical enforcement challenges.
  • Stakeholders should conduct comprehensive freedom-to-operate analyses considering existing patents and prior art.
  • Effective patent strategies involve aligning claims to withstand local invalidity grounds while securing competitive advantages.

FAQs

Q1: How does Mexican patent law define a patentable pharmaceutical invention?
A1: Mexican law requires the invention to be new, inventive, and industrially applicable, with specific criteria for pharmaceuticals relating to novelty of the composition or process as supported by the description.

Q2: Can MX2018000179 be challenged or invalidated?
A2: Yes, through legal proceedings such as declaratory judgment or opposition based on prior art, lack of novelty, or obviousness, especially if prior similar formulations exist.

Q3: How can companies design around this patent?
A3: By developing alternative formulations, using different active ingredients, or modifying synthesis processes that fall outside the scope of claims.

Q4: What is the typical duration of patent protection in Mexico?
A4: Twenty years from the date of filing, subject to maintenance fees; patent term extensions are rare but can apply in certain cases.

Q5: Does the patent provide exclusive rights across Latin America?
A5: No, it covers only Mexico. For regional protection, separate patents or regional filings (e.g., within the ARIPO or through PCT applications) are necessary.


References:
[1] Mexican Institute of Industrial Property (IMPI). Patent Database.
[2] Mexican Patent Law (Ley de la Propiedad Industrial).
[3] WIPO. PCT Patent Systems.
[4] Recent Mexican pharmaceutical patent filings and legal cases.

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.