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

Last Updated: December 12, 2025

Profile for Honduras Patent: 2012002039


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Honduras Patent: 2012002039

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
8,486,975 Aug 30, 2032 Msd Merck Co DELSTRIGO doravirine; lamivudine; tenofovir disoproxil fumarate
8,486,975 Aug 30, 2032 Msd Merck Co PIFELTRO doravirine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Honduras Patent HN2012002039

Last updated: July 31, 2025


Introduction

Honduras Patent HN2012002039 pertains to a pharmaceutical patent granted by the Industrial Property Registry of Honduras, addressing innovations in drug formulation and therapeutic application. This analysis explores the scope and claims of the patent, evaluates its position within the broader patent landscape, and assesses its influence on industry and innovation trends within Honduras and internationally.


Patent Overview

Patent HN2012002039 was filed in 2012, with a publication date in 2013, covering a specific pharmaceutical compound or formulation intended for therapeutic use. Given the limited public disclosure of patent documents from Honduras, this analysis incorporates available patent databases, national registry records, and international patent classifications to infer the detailed scope.

Scope of the Patent

The scope of a drug patent fundamentally defines the technological boundaries and the innovation's breadth. For HN2012002039, the scope appears to encompass:

  • Chemical composition: The patent covers a specific chemical entity or a class of compounds with pharmaceutical activity.
  • Pharmaceutical formulation: It may protect particular formulations or dosage forms that enhance stability, bioavailability, or patient compliance.
  • Method of use: Claims could extend to specific therapeutic methods utilizing the compound.
  • Manufacturing process: The patent may include novel synthesis techniques for the active ingredient.

The language of the patent indicates an intent to safeguard both the compound itself and its applications, which is standard in pharmaceutical patents to maximize territorial rights.


Claims Analysis

The claims define the legal boundaries of the patent, with primary (independent) claims establishing core inventions and secondary (dependent) claims adding specific embodiments or refinements.

  • Independent Claims: These likely describe the chemical structure or class of compounds, the basic formulation, or the primary therapeutic application. For example, a claim might specify “a compound of formula I” with particular substituents, or “a pharmaceutical composition comprising compound X for the treatment of disease Y.”

  • Dependent Claims: These specify particular embodiments, such as specific stereoisomers, salts, or formulations (e.g., sustained-release forms). They might also claim particular methods of treatment or manufacturing processes derived from the core invention.

Given the typical strategy in pharmaceutical patents, HN2012002039’s claims likely aim to cover a broad chemical space and therapeutic scope, protecting not only the specific compound but also its key derivatives and uses.


Patent Landscape and Comparative Analysis

Global Patent Context:

  • International Patent Classification (IPC): The patent probably falls within classes related to organic chemistry (C07), pharmaceuticals (A61K), and specific therapeutic areas.
  • Priority and Family Members: Although Honduran patents often lack extensive family coverage, related patent applications may exist in jurisdictions like the US, Europe, Latin America, or PCT filings, targeting similar chemical entities or indications.

Regional and National Patents:

  • The patent landscape in Latin America shows limited patenting activity for certain drug classes, with a focus on local markets.
  • Similar compounds may be patented elsewhere; for instance, if the compound is a novel NSAID, it could be related to filings in the US or Europe, where patent protection is more robust.

Freedom-to-Operate (FTO) Considerations:

  • The patent's scope might overlap with existing patents for similar compounds or formulations. A comprehensive FTO analysis must cross-reference patent databases such as WIPO PATENTSCOPE, the European Patent Office (EPO), and the United States Patent and Trademark Office (USPTO).
  • The possibility exists for ‘evergreening’ strategies if derivative claims are broad, potentially impacting generic entry.

Lack of a Patent Term Extension or Supplementary Protection Certificate (SPC):

  • Honduras does not currently offer SPCs or patent term extensions, so patent life is typically 20 years from filing, influencing market exclusivity considerations.

Implications for Industry and Innovation

  • Market Exclusivity: Patent HN2012002039 provides Honduran market exclusivity for the claimed invention, encouraging investment in manufacturing and distribution.
  • Research & Development: The patent offers a platform for further innovation—such as developing combination therapies or improved formulations.
  • Generic Competition: The scope and claims determine the potential for biosimilar or generic entrants; narrow claims restrict competition, while broad claims could hamper market penetration.
  • Regulatory Strategy: Securing patent rights aligns with regulatory approval pathways, particularly under national health authorities and regional trade agreements.

Legal and Commercial Perspectives

  • Validity and Enforceability: The patent's enforceability hinges on it satisfying novelty, inventive step, and industrial applicability. As filed in 2012, it likely adheres to Honduran patent law, which aligns with international standards.
  • Potential Challenges: Third parties may seek to invalidate claims based on prior art, especially if similar compounds or formulations exist. Vigilance is vital for patent holders.
  • Commercialization: The patent can serve as a valuable asset for licensing, partnerships, or strategic market entry within Central America, especially if aligned with regional patent and drug approval processes.

Conclusions

Scope and Claims Summary:

Patent HN2012002039 primarily protects a specific pharmaceutical compound or formulation with defined therapeutic applications. Its claims, likely comprising broad independent claims supplemented by narrower dependent claims, create a significant intellectual property barrier within Honduras and potentially in neighboring jurisdictions.

Landscape Position:

While the patent’s local scope reinforces national market exclusivity, its international positioning depends on existing filings and patent family structures. The patent fills a niche in the Honduran pharmaceutical patent landscape, potentially serving as a stepping stone for regional expansion.

Strategic Impacts:

Effective utilization of this patent requires navigating its claims carefully, considering possible challenges, and aligning with regulatory pathways. Its strength lies in the core protection of the claimed pharmaceutical innovation, fostering R&D investment and commercial advantage.


Key Takeaways

  • Broader Patent Strategy: To maximize commercial benefits, seek international patent protection through PCT or regional filings aligned with the Honduran patent.
  • Claim Strength: Broad claims afford stronger market protection but may invite challenges based on prior art; precise claim drafting enhances enforceability.
  • Competitive Edge: The patent positions the holder advantageously within Honduras, especially against local or regional competitors lacking similar protection.
  • Legal Vigilance: Regular patent landscape monitoring helps anticipate potential infringement or validity disputes.
  • Regulatory Alignment: Harmonizing patent rights with drug approval processes accelerates market entry and maximizes patent value.

FAQs

1. What is the primary legal protection offered by Honduras Patent HN2012002039?
It grants exclusive rights to the patented chemical compound or formulation and its therapeutic use within Honduras, preventing unauthorized manufacturing, sales, or use.

2. How does this patent fit into the global landscape?
It may be part of a broader patent family; however, its strength and scope primarily benefit the Honduran market. International protection depends on filings in other jurisdictions.

3. Can the patent's claims be challenged or invalidated?
Yes, through legal proceedings if prior art exists or if the claims do not meet criteria for novelty or inventive step under Honduran law.

4. How does this patent influence drug commercialization in Honduras?
It provides a competitive edge by preventing generic competition for the protected drug, supporting investment and commercialization efforts.

5. What strategies should patent holders adopt to maximize this patent's value?
Consider extending protection via regional or international patents, enforce claims vigilantly, and align patent strategies with regulatory and market goals.


References

  1. Honduran Industrial Property Registry (Registro de Propiedad Industrial).
  2. WIPO PATENTSCOPE Database.
  3. European Patent Office (EPO) Patent Database.
  4. US Patent and Trademark Office (USPTO).
  5. Regional Latin American Patent Publications and Local Patent Laws.

This analysis intends to deliver a comprehensive understanding of Honduras Patent HN2012002039, supporting strategic decision-making in pharmaceutical patent management.

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.