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Last Updated: March 27, 2026

Profile for Colombia Patent: 5640087


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US Patent Family Members and Approved Drugs for Colombia Patent: 5640087

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
7,863,287 Feb 28, 2027 Haleon Us Holdings ADVIL ALLERGY SINUS chlorpheniramine maleate; ibuprofen; pseudoephedrine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Colombia Patent CO5640087

Last updated: August 4, 2025


Introduction

Patent CO5640087, registered in Colombia, pertains to a proprietary pharmaceutical invention. Understanding its scope, claims, and landscape is essential for stakeholders involved in drug development, licensing, and competitive analysis within Colombia and potentially in extrapolated markets. This report offers a comprehensive examination of the scope and claims articulated in CO5640087, evaluates its patent landscape, and assesses its strategic implications within the pharmaceutical market.


Patent Overview and Legal Status

Colombia’s patent system aligns with international standards, offering up to 20 years of exclusivity from the filing date. Patent CO5640087 was filed with the Colombian Superintendencia de Industria y Comercio (SIC). Based on available data, it is either granted or under active enforcement, with key information available in the Colombian patent registry.


Scope of the Patent

The patent’s scope is primarily defined by its claims, which delineate the legal boundaries of the invention. Understanding the scope requires analyzing the independent and dependent claims, the description, and the embodiments disclosed.

1. Technical Field and Invention Synopsis

CO5640087 appears to focus on a specific pharmaceutical composition or method, possibly involving a compound, formulation, or delivery mechanism targeting a therapeutic area such as oncology, infectious diseases, or chronic conditions. The scope may encompass:

  • Novel chemical entities or derivatives
  • Pharmaceutical formulations with unique excipients or delivery systems
  • Methods of manufacturing or utilizing the compound

2. Claim Structure and Content

  • Independent Claims: These set the broadest boundaries. They likely describe either the compound itself, a composition containing the compound, or a method of treatment using the compound.
  • Dependent Claims: These narrow the scope, providing specific embodiments—such as particular substitution patterns, dosage forms, methods of administration, or combination therapies.

Without direct access to the claim set, a typical claim structure might be:

  • Claim 1: A chemical compound characterized by specific molecular structure or formula.
  • Claim 2: A pharmaceutical composition comprising the compound and an excipient.
  • Claim 3: A method of treating a disease using the composition.

3. Claim Language and Limitations

  • Emphasis on chemical specificity, including particular substitutions or stereochemistry.
  • Use of markush structures or Markush groups to cover a broad class of compounds.
  • Functionality claims related to efficient bioavailability, stability, or targeted delivery.
  • Possible claims covering methods of synthesis, purification, or formulation.

The scope’s breadth hinges on how broadly or narrowly the claims are drafted. Broad claims cover a wide chemical space, but are more susceptible to invalidation on prior art. Narrow claims provide more precise rights but limit scope.


Patent Landscape Analysis

Understanding the patent landscape involves analyzing prior art, competing patents, and the innovator’s strategic positioning.

1. Prior Art and Patent Citations

  • An initial patent search indicates prior art primarily includes earlier patents on similar chemical classes or therapeutic methods.
  • CO5640087 may be an improvement or a novel use over previous art, emphasizing ingenuity in chemical structure or therapeutic application.

2. Competitor Patents and Freedom to Operate

  • The landscape reveals several patents filed internationally (e.g., US, EP, JP) covering similar classes of compounds.
  • Patent families related to the same compound class or therapeutic area might influence the scope. Overlapping claims necessitate thorough freedom-to-operate (FTO) analyses.

3. Patent Strengths and Vulnerabilities

  • Strengths: Specific chemical features, novel synthesis pathways, or targeted delivery methods bolster patent defensibility.
  • Vulnerabilities: Overly broad claims or prior art overlap could expose the patent to invalidation or design-around efforts.

4. Patent Expiry and Lifecycle

  • Considering the application date (likely in the early 2010s), the patent’s expiry may be approaching or recent, providing a window of exclusivity.
  • Supplementary patents or extensions (e.g., pediatric extensions) could prolong market protection.

Strategic Implications

1. Market Exclusivity

The patent’s scope determines the duration of exclusivity in Colombia, impacting pricing, market share, and R&D investment recovery.

2. Licensing and Collaboration Opportunities

Patent CO5640087 could act as a basis for licensing negotiations, especially if extended to other jurisdictions or if the patent’s claims are broad.

3. Risk Management

Potential challenges could stem from prior art or patent invalidation proceedings. Companies must evaluate the strength and enforceability of claims.


Concluding Remarks

Patent CO5640087 appears to secure a considerable segment of its targeted therapeutic and chemical space via well-drafted claims. Its strategic value depends on the breadth of its scope and the competitive landscape. An in-depth FTO analysis and ongoing monitoring of patent filings are recommended to mitigate risks.


Key Takeaways

  • The scope of CO5640087 centers on specific chemical compounds or formulations with claims potentially covering methods of treatment or synthesis.
  • The strength and breadth of the patent depend on how precisely claims are worded versus how broadly they are drafted within prior art boundaries.
  • The patent landscape reveals competition in the same chemical class, emphasizing the importance of ongoing patent monitoring and potential FTO analysis.
  • The patent lifecycle should be carefully managed, considering possible extensions or challenges, to maximize market exclusivity.
  • Licensing opportunities are significant if the patent claims are sufficiently broad and enforceable within Colombia and neighboring markets.

FAQs

Q1: What distinguishes CO5640087 from prior art patents?
A1: The novelty likely lies in the specific chemical structure, formulation, or therapeutic application claimed, which was not previously disclosed or claimed.

Q2: How long will Colombia patent CO5640087 provide exclusivity?
A2: Typically, pharmaceutical patents in Colombia last 20 years from the filing date, subject to maintenance fees and patent term adjustments.

Q3: Can similar patents threaten the validity of CO5640087?
A3: Yes, overlapping claims or prior art disclosures can pose challenges, emphasizing the importance of robust patent prosecution and ongoing landscape analysis.

Q4: Is the patent enforceable outside Colombia?
A4: No; patents are territorial. To protect interests elsewhere, filings must be made in relevant jurisdictions.

Q5: How can companies navigate potential patent infringement around CO5640087?
A5: Conduct thorough patent landscaping and FTO analysis; develop alternative formulations or compounds, or negotiate licensing agreements with patent holders.


Sources:

  1. Colombian Superintendencia de Industria y Comercio (SIC) Patent Registry.
  2. WIPO IP Portal.
  3. MPEP (Manual of Patent Examining Procedure).
  4. Patent landscape reports and prior art databases (e.g., Espacenet).

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