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

Last Updated: December 18, 2025

Profile for Honduras Patent: 2011000699


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Honduras Patent: 2011000699

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 Apr 29, 2033 Novartis VIJOICE alpelisib
⤷  Get Started Free Apr 29, 2033 Novartis PIQRAY alpelisib
⤷  Get Started Free Sep 10, 2029 Novartis VIJOICE alpelisib
⤷  Get Started Free Sep 10, 2029 Novartis PIQRAY alpelisib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Honduras Drug Patent HN2011000699

Last updated: August 1, 2025


Introduction

The patent HN2011000699, filed and granted in Honduras, centers on a pharmaceutical invention. As a key asset in the country's patent landscape, understanding its scope and claims is crucial for stakeholders involved in drug development, licensing, intellectual property strategies, and market competition. This report provides an in-depth analysis of the patent's scope, claims, and its positioning within the global patent environment.


Overview of Honduran Patent HN2011000699

Honduras, under its intellectual property laws aligned with the Andean Community and TRIPS (Trade-Related Aspects of Intellectual Property Rights), grants patents that typically have a 20-year term from the filing date. Patent HN2011000699 was likely filed around 2011, given its publication number, and consequently, its expiration date would be approximately 2031, assuming maintenance fees are paid.

The patent relates to a specific pharmaceutical composition or process, claiming innovations that potentially target a particular therapeutic indication. The scope of protection hinges on the precise wording of the claims, which delineate the invention's boundaries.


Scope of the Patent: Analyzing the Claims

Claims Structure and Types

Patent claims are the defining legal boundaries that determine the scope of protection. In pharmaceutical patents, claims often fall into two categories:

  • Product claims – Cover the chemical entities, compositions, or formulations.
  • Process claims – Encompass the methods of manufacturing or use.

For HN2011000699, the claims are presumed to include:

  • Independent Claims: Broadly define the core invention—possibly a novel drug compound or formulation.
  • Dependent Claims: Narrower claims that specify particular embodiments, such as dosage forms, concentration ranges, or methods of administration.

Key Claim Elements

Although the explicit language requires access to the original patent document, in typical pharmaceutical patents, the claims may incorporate:

  • Novel compound or derivatives: Claiming unique chemical entities or modifications.
  • Pharmaceutical compositions: Encompassing specific combinations of active ingredients with excipients.
  • Method of treatment: Claims that cover administering the compound for particular therapeutic indications.
  • Manufacturing process: Innovations in synthesis or formulation techniques.

Scope Analysis

  • Breadth: The scope’s breadth is determined by how broad the independent claims are drafted. If broad, they could potentially cover a wide class of compounds or use methods.
  • Specificity: Narrow claims tied to specific compounds or doses limit third-party infringement but provide strong protection for the claimed embodiments.
  • Potential for Patent Thicket: Multiple dependent claims covering various embodiments can create layered protection but may also invite patent clearance complexities.

Legal Robustness

The enforceability of these claims depends on:

  • Novelty: The claims must distinguish from prior art. In the pharmaceutical realm, this involves demonstrating new chemical structures, unexpected results, or novel therapeutic uses.
  • Inventive Step: The claims should involve an inventive step over existing drugs, formulations, or processes.
  • Clarity and Support: The claims must be clear and supported by the description and drawings.

Patent Landscape Context

Global Patent Environment

Honduras, while a member of the TRIPS Agreement, has a relatively nascent pharmaceutical patent landscape compared to jurisdictions like the US, EU, or China. Nonetheless, the patent likely aligns with international standards, facilitating potential extensions or family filings elsewhere.

Comparative Patent Landscape

  • Regional Patents: In Latin America, similar patents may exist in countries with more comprehensive pharmaceutical patent regimes, such as Mexico and Brazil.
  • Patent Families: Inventors often file patent families to secure protection across multiple jurisdictions; the absence or presence of such extensions influences the freedom-to-operate.

Prior Art and Innovation Landscape

The scope and strength of claims depend heavily on prior art:

  • Chemical Databases: Known drugs and chemical structures from the Merck Index, PubChem, or patent databases.
  • Literature: Scientific publications revealing similar compounds or formulations.
  • Existing Patents: Prior patents, especially those from multinational pharmaceutical companies, that may have overlapping claims.

An analysis of patent databases (e.g., Espacenet, INPI, EPO) indicates whether comparable patents exist, which dictates patent validity and enforcement potential in Honduras and beyond.

Infringement and Freedom-to-Operate

Given the possible scope, competitors must evaluate:

  • Whether their drug candidates or manufacturing processes infringe on claim scope.
  • The risk of invalidation based on prior art challenges.
  • Opportunities for licensing or cross-licensing agreements.

Legal and Commercial Significance

The patent's broad or narrow claims directly impact:

  • Market exclusivity: Protects the innovator’s commercial interests.
  • Research and development: Defines the-able to change or improve the patented invention.
  • Compulsory licensing risks: In some jurisdictions, overly broad claims may trigger gov’t intervention in public health crises.

In Honduras, enforcement depends on local courts, but the patent provides a foundation for legal action against infringers, assuming proper maintenance and valuation.


Conclusion

Patent HN2011000699 encapsulates a pharmaceutical invention with protected claims that likely cover a specific compound, formulation, or therapeutic application. The scope, dictated by claim language, is critical for determining enforcement rights and potential overlap with other patents. Its landscape in Honduras is modest but integral within the Latin American pharmaceutical patent domain, presenting valuable exclusivity for the patent holder in the regional market.


Key Takeaways

  • The patent's claims define the extent of protection; broad claims offer wider rights but face higher validity hurdles.
  • The scope influences strategic considerations such as licensing, legal enforcement, and R&D focus.
  • Cross-jurisdiction patent filings can extend protection and mitigate risk from regional patent challenges.
  • Regular patent landscape analysis is necessary to monitor potential infringements and avoid patent thickets.
  • Engagement with local legal counsel enhances enforcement effectiveness and compliance in Honduras.

FAQs

1. What is the primary legal significance of patent HN2011000699?
It grants exclusive rights to the patent holder within Honduras, preventing competitors from manufacturing, using, selling, or importing the patented pharmaceutical invention without permission.

2. Can the scope of the patent's claims be challenged or narrowed?
Yes. During patent opposition or litigation, claims can be challenged for lack of novelty or inventive step, potentially leading to narrowing or invalidation.

3. How does the patent landscape in Honduras compare to other Latin American countries?
Honduras's patent environment is less mature and has fewer filings compared to countries like Mexico and Brazil; however, harmonized treaties facilitate regional patent protection.

4. Is this patent commercially valuable outside Honduras?
Potentially, if similar or identical filings exist elsewhere. Patent families or international applications (via PCT routes) extend protection and maximize market exclusivity.

5. What strategic steps should a pharmaceutical company consider regarding this patent?
Assess infringement risks, explore licensing opportunities, monitor local enforcement, and consider patenting innovations that improve or modify the protected invention.


References

  1. Honduras Intellectual Property Office (CPI). Official patent granting procedures and legal standards.
  2. TRIPS Agreement. Minimum standards of patent protection protected under WTO.
  3. European Patent Office (EPO). Patent landscape analyses and searching tools for prior art.
  4. WIPO Patent Scope Database. For patent family and related family data.
  5. Latin American Patent Databases. Comparative insights on regional patent protections and filings.

Note: Access to the full patent document is necessary for a precise claim-by-claim analysis and to confirm specific claim language. This report is based on typical patent structures and available background information.

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.