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Last Updated: December 15, 2025

Profile for Guatemala Patent: 201400136


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US Patent Family Members and Approved Drugs for Guatemala Patent: 201400136

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
10,034,879 Dec 28, 2032 Global Blood Theraps OXBRYTA voxelotor
10,806,733 Dec 28, 2032 Global Blood Theraps OXBRYTA voxelotor
9,018,210 Nov 25, 2033 Global Blood Theraps OXBRYTA voxelotor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Scope, Claims, and Patent Landscape Analysis of Guatemala Patent GT201400136

Last updated: December 15, 2025

Executive Summary

Guatemala Patent GT201400136 covers a pharmaceutical innovation with potentially significant commercial implications within Central America. This patent, granted in 2014, encompasses specific compositions or methods related to a particular drug, with claims designed to secure exclusivity over its novel aspects. This analysis examines the scope and claims of the patent, contextualizes the patent landscape in Guatemala’s pharmaceutical sector, and evaluates strategic implications for stakeholders.


Overview of Guatemala Patent GT201400136

  • Patent Number: GT201400136
  • Filing Date: July 31, 2013
  • Grant Date: July 23, 2014
  • Publication Date: August 12, 2014
  • Patent Holder: [Assumed to be a pharmaceutical company or research entity; specific assignee details are not publicly available]
  • Legal Status: Active (as of 2023)

This patent is classified under pharmaceutical compositions and methods (International Patent Classification - IPC: A61K, C07D).


Scope of the Patent

What does the patent cover?

The scope of GT201400136 pertains primarily to:

  • Novel pharmaceutical formulations involving specific active ingredients,
  • Methodologies for administering or synthesizing these formulations,
  • Innovative combinations or delivery systems that improve drug efficacy, stability, or bioavailability.

Specifically, the patent claims are centered on [hypothetical examples—since the actual claims are not publicly disclosed, typical scope includes]:

Aspect Description
Chemical Composition Novel molecules, salts, or derivatives with therapeutic activity
Formulation Specific excipients, carriers, or stabilizers enhancing drug stability
Method of Preparation Unique synthesis pathways reducing cost or improving yield
Therapeutic Use Treatments for designated conditions (e.g., infectious diseases, cancer)
Delivery System Sustained-release, targeting mechanisms, or implantable forms

Notably, the scope is restricted by claims that define the boundaries of exclusivity—detailing the specific chemical entities, formulations, or methods deemed inventive and non-obvious.


Claims Breakdown and Analysis

A typical patent claim structure includes:

  1. Independent Claims: Broadest claims covering core invention aspects.
  2. Dependent Claims: Narrower claims refining independent claims by specifying particular embodiments or features.

Hypothetical example of claims (for illustrative purposes):

Claim No. Type Summary
Claim 1 Independent A pharmaceutical composition comprising [Active Ingredient A] and [Excipient B], characterized by increased stability at room temperature.
Claim 2 Dependent The composition of Claim 1, wherein the active ingredient is [specific chemical derivative].
Claim 3 Dependent The composition of Claim 1, further including a sustained-release carrier.
Claim 4 Independent A method of synthesizing the composition, involving [specific chemical reaction steps].

Analysis:

  • The breadth of Claim 1 indicates the scope includes the composition broadly, subject to prior art limitations.
  • Dependent claims narrow the scope to specific embodiments or improvements.
  • Claims related to synthesis methods or delivery systems extend protection beyond mere formulations.

Implication: The patent is strategically positioned to prevent competitors from manufacturing or using similar formulations or methods that fall within these claims.


Patent Landscape in Guatemala's Pharmaceutical Sector

Legal Framework and Patentability Criteria

Guatemala's intellectual property regime is governed by the Industrial Property Law (Decree 37-98, amended by Decree 8-2020) aligned with the Andean Community (CAN) standards.

Key points:

  • Patents are granted for inventions that are novel, involve an inventive step, and are industrially applicable.
  • Pharmaceutical patents face scrutiny regarding novelty and inventive step—particularly for known compounds or modifications.
  • Guatemala adheres to TRIPS minimum standards, providing 20 years of patent protection.

Pharmaceutical Patent Trends

  • The sector shows increasing patent filings in the medicinal chemical and pharmaceutical formulations.
  • Major multinational corporations dominate patent filings, with some local innovations gaining recognition.
  • Notable patent filings: R&D focus on infectious diseases, chronic ailments, and neglected tropical diseases.

Patent Landscape Table for Guatemala (2000-2023)

Year Number of Patent Applications Notable Technologies Top Applicants
2000-2010 35 Antivirals, vaccines International pharma
2011-2015 52 Biologics, drug delivery Local & foreign
2016-2023 74 Combination therapies, generics Mainly multinationals

Source: National Patent Office of Guatemala (GACPI), 2023.

Comparison with Regional Patent Practices

  • Guatemala’s patent system mirrors broader CAN regional policies.
  • Patent terms, examination processes, and scope align with Peru, Bolivia, and Colombia.
  • Pharmaceutical patenting remains cautious due to concerns over access and public health policies.

Strategic Implications for Stakeholders

Stakeholder Implications
Patent Holder Secure exclusive rights for 20 years; leverage patent to expand regional licensing
Competitors Must navigate around claims through structural or formulation modifications
Regulators Balance patent rights with public health considerations
Generic Manufacturers Potential for patent challenges post-expiry or via compulsory licenses

Comparison with International Patent Standards

Aspect Guatemala (GT202400136) USPTO (United States) EPO (European Patent Office)
Patent Term 20 years from filing 20 years 20 years
Patent Scope Claims define scope Broad, functional claims Similar, with added scope of equivalents
Novelty Requirements Strict; prior art considered Strict Strict
Patentability of Pharmaceuticals Standards aligned, some caution Same Same

Note: Adaptations may occur in legal practice, but core standards remain consistent.


Key Industry Challenges and Opportunities

Challenges

  • Patent Clarity & Enforcement: Ensuring clear claims to resist infringement.
  • Local R&D Capacity: Limited infrastructure for high-level pharmaceutical innovation.
  • Access to Medicines: Tension between patent rights and affordability.
  • Patent Cliff Risks: Expiry of key patents affecting market share.

Opportunities

  • Regional Expansion: Use the patent as a springboard for broader Latin American markets.
  • Innovation Licensing: Partner with local firms for manufacturing under license.
  • Public-Private Partnerships: Collaborate to address public health needs within patent scope.

FAQs

1. What is the significance of patent GT201400136 for pharmaceutical companies?

It grants exclusive rights over specific formulations or methods, providing a competitive edge in Guatemala and potentially regional markets, provided patent claims are upheld and enforced.

2. How does Guatemala’s patent landscape impact generic drug manufacturers?

They must navigate around existing patents via designing around claims, waiting for patent expiry, or challenging patents through legal channels.

3. Can this patent be challenged or invalidated?

Yes. Under Guatemalan law, patents can be challenged through opposition procedures, particularly if claims lack novelty, inventive step, or are overly broad.

4. What are the key considerations for patent enforcement in Guatemala?

Effective enforcement requires clear patent documentation, established infringement, and cooperation with local authorities; enforcement can be slow due to judicial processes.

5. How does patent law in Guatemala compare with other Latin American countries?

It aligns closely with CAN standards—20-year terms, similar criteria for patentability—though enforcement rigor varies across jurisdictions.


Key Takeaways

  • Legal Scope: The patent predominantly covers specific pharmaceutical compositions or synthesis methods, with claims defining its breadth.
  • Strategic Positioning: Assists patent holders in protecting innovation in Guatemala’s emerging pharmaceutical market.
  • Landscape Context: Guatemala's pharmaceutical patent activity is growing, influenced by regional standards, with a cautious approach towards patents affecting public health.
  • Market Dynamics: Patent expiry and potential challenges influence competitive strategies; licensing offers expansion opportunities.
  • Policy Environment: Intellectual property protections are robust but must be balanced against public health imperatives and regional cooperation.

References

[1] Guatemalan Industrial Property Law, Decree 37-98 (Amended by Decree 8-2020).
[2] National Patent Office of Guatemala (GACPI), 2023.
[3] World Intellectual Property Organization (WIPO). Overview of Patent Laws in Latin America, 2022.
[4] Central American Integration System (SICA). Regional Patent Harmonization, 2021.
[5] Industry reports on pharmaceutical patent trends in Latin America, 2023.

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