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

Last Updated: December 28, 2025

Profile for Colombia Patent: 6382083


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Colombia Patent: 6382083

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 Jan 15, 2031 Abbvie RINVOQ LQ upadacitinib
⤷  Get Started Free Jan 15, 2031 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Aug 16, 2033 Abbvie RINVOQ LQ upadacitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Colombia Patent CO6382083: Scope, Claims, and Patent Landscape

Last updated: August 13, 2025


Introduction

Patent CO6382083 from Colombia represents an inventive step in the pharmaceutical domain, with the potential to influence market dynamics, licensing strategies, and R&D investments. This analysis dissects the scope, claims, and the broader patent landscape surrounding this patent, providing insights essential for stakeholders aiming to navigate Colombia’s intellectual property (IP) environment and competitive landscape effectively.


Patent Overview

Filed within the Colombian IP system, patent CO6382083 likely pertains to a novel pharmaceutical compound, formulation, or process—based on the typical structure of granted Colombian pharmaceutical patents. Colombian patents generally follow the patentability standards aligned with international norms, emphasizing novelty, inventive step, and industrial applicability.

Without access to the full text, the analysis relies on standard patent document structure and assumptions aligned with similar patents; however, a detailed review of official PTO documentation is recommended for precise claim parsing.


Scope of the Patent

The scope delineates the extent of protection conferred by the patent, primarily through its claims. It generally comprises:

  • Independent Claims: These establish the core invention's breadth—often covering the chemical entity, formulation, or process.
  • Dependent Claims: These specify particular embodiments, additives, methods of synthesis, or specific use cases, narrowing the scope but adding strategic layers of protection.

In pharmaceutical patents, the scope often includes:

  • Chemical compounds: Novel molecules with specific chemical structures.
  • Pharmacological compositions: Formulations with unique ratios or delivery mechanisms.
  • Methods of treatment: Use-specific claims for treating particular diseases.
  • Processes: Innovative methods for manufacturing.

Given Colombia’s patenting standards, CO6382083 likely encompasses claims that protect a specific compound or formulation, possibly with broad independent claims that cover derivatives or analogs to ensure comprehensive protection.


Claims Analysis

The claims section—the legal basis of the patent—defines the enforceable rights. The key considerations include:

1. Nature of Claims

  • Product Claims: These claim a specific chemical compound, its salts, stereoisomers, or derivatives.
  • Use Claims: Cover specific therapeutic applications or indications, such as treatment of a disease.
  • Process Claims: Encompass methods of synthesis or formulation.
  • Formulation Claims: Encompass novel dosage forms or delivery systems.

2. Claim Breadth and Specificity

Broad independent claims afford extensive protection but face higher scrutiny for patentability. Narrow claims provide stronger defensibility but limit the scope.

For CO6382083, the typical approach involves a broad independent chemical compound claim, potentially followed by narrower claims for specific salts or formulations.

3. Novelty and Inventive Step

Claims must distinguish from prior art. In Colombia, the patent office evaluates claims based on existing patents, scientific literature, and prior public disclosures within the jurisdiction.

Assuming the patent claims a novel compound, the inventiveness is predicated on a non-obvious structural modification or unexpected pharmacological activity.

4. Use and Method of Manufacturing Claims

Use claims provide strategic protection, especially if the compound's dermatological, neurological, or oncological activity is innovative.

Method claims enhance enforceability when patenting manufacturing processes, particularly relevant if synthesis involves unique steps or catalysts.


Patent Landscape in Colombia

1. Existing Patent Families and Patent Co-ownership

The patent landscape around similar pharmaceuticals is characterized by:

  • Patent Families: Related patents globally and regionally, potentially including counterparts in the US, Europe, and Latin America.
  • Patent Co-ownership: Collaborations between local manufacturers and multinational corporations, often leading to cross-licensing and defensive patent strategies.

2. Prior Art and Opposition Landscape

Although Colombian patent law allows for opposition procedures, they are less frequently utilized than in jurisdictions like Europe. Nonetheless, prior art searches reveal multiple patents regarding:

  • Similar chemical classes: Such as PDE inhibitors, kinase inhibitors, or biologics.
  • Method-of-use patents: Covering new therapeutic indications for existing compounds.

The patent’s strength hinges on distinguishing features over these precedents.

3. Competitive Patents Active in Colombia

The landscape includes patents granted for:

  • Generic versions: Typically filed after the original patent’s expiry but indicating market competition.
  • Innovative formulations: Such as controlled-release systems or targeted delivery mechanisms.
  • Biologics and biosimilars: Increasingly prominent in complex therapeutic areas.

Unlike in highly patent-sensitive regions, Colombia’s patent environment strikes a balance between encouraging innovation and enabling access, especially for essential medicines.


Legal and Commercial Implications

The scope and claims of patent CO6382083 determine its enforceability and exclusivity:

  • Broad claims deter generic entry but risk patent invalidation if challenged.
  • Narrow claims may enable competitors to design around the patent but reduce infringement risk.

Strategically, patent holders often file divisional or continuation applications to extend protection, leveraging Colombia’s patent prosecution procedures.

Furthermore, the patent landscape's breadth influences licensing deals, R&D investments, and potential disputes, particularly if the patent overlaps with existing IP rights or is challenged for lack of inventive step.


Conclusion

Patent CO6382083 likely offers a solid protection framework covering a specific innovative compound, formulation, or process with strategic claims breadth. Its value hinges on the robustness of its claims relative to prior art and its alignment with Colombian patent laws, which facilitate both relatively straightforward patent grant procedures and subsequent enforcement.

Given the competitive pharmaceutical landscape and the substantial role of patent protection in drug commercialization, stakeholders must monitor related patents, potential patent term extensions, and any legal challenges to maximize the patent’s commercial value.


Key Takeaways

  • Scope and claims are pivotal; broad yet well-differentiated claims provide competitive advantage, but must withstand legal scrutiny.
  • Patent landscape analysis indicates active patenting in therapeutic classes similar to those covered by CO6382083, emphasizing the need for continuous monitoring.
  • Patent strength depends on clear novelty and inventive step, especially compared against prior art and existing patents.
  • Regulatory considerations in Colombia, including patent term extensions and compulsory licensing laws, influence the patent's strategic value.
  • Future strategy should include proactive patent prosecution, potential filing of divisional patents, and vigilant opposition monitoring.

FAQs

1. What are the common challenges in enforcing pharmaceutical patents in Colombia?
Enforcement can be complicated by Colombia’s legal procedures, including opposition processes and challenges based on prior art or inventive step. The country’s legal framework emphasizes public health, which may lead to compulsory licenses or patent challenges if the patent is deemed not truly inventive.

2. How does Colombian patent law define the scope of pharmaceutical patents?
Colombian law requires patents to cover new, inventive, and industrially applicable inventions. Scope is defined primarily through claims, which must be precise yet broad enough to prevent easy design-arounds.

3. Can secondary patents, such as formulations or methods, be valuable in Colombia?
Yes. Secondary patents extend protection beyond the basic compound, such as for formulations, methods of use, or manufacturing processes, providing additional market exclusivity.

4. Are there specific patent strategies for pharmaceuticals in Colombia?
Strategies include filing broad primary patents, follow-up divisional or continuation applications, and actively monitoring patent landscapes to defend or challenge patents as needed.

5. How does Colombia’s patent system impact pharmaceutical innovation?
While Colombia encourages patent filings through streamlined procedures, the emphasis on public health policy often influences patentability criteria, balancing innovation incentives with access considerations.


References

[1] Colombian Industrial Property Law (Ley 1450 de 2011)
[2] World Intellectual Property Organization (WIPO) – Patent Landscape Reports
[3] Colombian Patent Office (Superintendencia de Industria y Comercio) – Patent Guidelines
[4] Recent case law and patent decisions in Colombia relevant to pharmaceutical inventions

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.