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

Last Updated: December 18, 2025

Profile for Colombia Patent: 2021015067


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Colombia Patent: 2021015067

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 Aug 5, 2041 Pfizer PAXLOVID (COPACKAGED) nirmatrelvir; ritonavir
⤷  Get Started Free Oct 31, 2041 Pfizer PAXLOVID (COPACKAGED) nirmatrelvir; ritonavir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Colombia Patent CO2021015067

Last updated: August 5, 2025

Introduction

Colombia Patent CO2021015067, granted in 2021, pertains to an innovative formulation or method involving a pharmaceutical compound or combination. Its scope, claims, and landscape analysis reveal significant insights into its innovation breadth, competitive positioning, and potential implications within the Colombian and global pharmaceutical patent environment. This review systematically dissects these elements to facilitate strategic decision-making for stakeholders.


Patent Overview and Context

Colombia's patent system aligns with international standards, notably TRIPS, providing robust protection for pharmaceutical innovations. Patent CO2021015067 encompasses a specific novel invention, likely related to a therapeutic compound or pharmaceutical formulation. The patent's filing and grant dates suggest an emphasis on recent technological advancements, possibly in specialized areas like biologics, novel delivery systems, or combination therapies.


Scope of the Patent

The scope of CO2021015067 primarily depends on its claims, which define the legal boundaries of protection. Here, the scope can be categorized into core and auxiliary claims:

Core Claims

The core claims typically cover the primary invention—say, a new compound, formulation, or method—embodying the inventive step. These claims articulate the fundamental features that distinguish it from prior art. For instance, if the patent centers on a novel drug delivery system, the claims would specify the unique structural or functional elements.

Dependent and Auxiliary Claims

Dependent claims refine the core claims, adding specific embodiments, such as particular dosages, use cases, or manufacturing methods. Auxiliary claims might extend the scope, covering alternative embodiments, different dosage forms, or methods of use, thus broadening the patent's protective envelope.

Geographic and Regulatory Scope

Being a Colombian patent, the geographic scope is initially national; however, its strategic value increases if the patent family extends to regional (e.g., Andean Community) or international filings via mechanisms like PCT. The scope's strength depends on claims' breadth and how well they withstand prior art challenges, especially in key therapeutic areas.


Claims Analysis

A detailed claims analysis requires examining the granted claims' language:

Independent Claims

These define the essential protection. For example, an independent claim might state:

"A pharmaceutical composition comprising Compound X and a carrier, wherein said composition is suitable for the treatment of Disease Y."

Such claims typically focus on:

  • The specific chemical structure or formulation.
  • The method of preparation or use.
  • The combination with other therapeutic agents.

Scope and Novelty

The novelty hinges on whether the claims introduce unique structural features, unexpected synergistic effects, or innovative delivery methods not previously disclosed. For example, if the claims cover a previously unknown polymorph of a drug, the scope could be quite narrow but highly valuable.

Claims Strength and Validity

  • Breadth: Broad claims offer extensive protection but face higher scrutiny for obviousness or inventive step.
  • Narrow Claims: Focused on specific compounds or methods, more defensible but potentially easier to circumvent.
  • Potential Overreach: Claims that attempt to cover too broad a territory risk invalidation if prior art exists.

Claim Dependencies

Dependent claims enhance scope by adding limitations—protecting specific embodiments—while also serving as fallbacks if broader claims are invalidated.


Patent Landscape in Colombia

The Colombian patent landscape for pharmaceuticals is characterized by:

Innovation Hotspots

Key areas include biopharmaceuticals, targeted therapies, and novel drug delivery platforms. Colombia's innovation activity is influenced by local research institutions, multinational corporations, and emerging biotech startups.

Patent Density and Filing Trends

Recent years show increasing patent filings in the pharmaceutical sector, emphasizing R&D efforts. The Colombian Patent Office (Superintendencia de Industria y Comercio) actively examines patents, with a trend toward stringent examination of inventive step and novelty.

Patent Family and Extension

While CO2021015067 is Colombian-specific, the patent family likely extends to regional (PCT) and international filings, reflecting a strategy for broader market protection.

Patent Challenges and Litigation

In Colombia, patent enforcement remains developing. Patent opposition and invalidation procedures are accessible and can influence the patent's enforceability and licensing potential.


Comparative and Competitive Landscape

Understanding the patent landscape involves assessing:

  • Existing Patents: Similar patents in Colombia and nearby jurisdictions (e.g., patents in Brazil, Mexico, or the US). Overlaps may indicate crowded fields or freedom-to-operate challenges.
  • First-to-File vs. First-to-Create: Colombia follows a first-inventor-to-file principle, making early filing crucial.
  • Patent Thickets: Overlapping claims by multiple patentees may complicate commercialization.
  • Innovation Clusters: Integration with research institutions or collaborations enhances patent strength and commercialization opportunities.

Implications for Stakeholders

Pharmaceutical Innovators

Strategic patent drafting (broad vs. narrow claims) balances breadth and defensibility. International filings enhance global competitiveness. Patent CO2021015067's positioning affects market exclusivity and potential licensing.

Generic Manufacturers

The patent landscape guides lifecycle management. Challenging weak claims or invalidating overly broad patents can open pathways for generics. Understanding claim scope is vital for designing non-infringing products.

Regulatory and Commercial Strategies

Patent protection supports regulatory exclusivity claims, facilitating market entry timing. Licensing deals hinge on patent strength and scope clarity.


Conclusion

Patent CO2021015067 encompasses a strategically significant piece within Colombia’s pharmaceutical IP framework. Its scope, predominantly governed by detailed claims, offers protection around a specific inventive concept. The breadth of those claims impacts enforcement, potential for litigation, and competitive positioning.

The overall patent landscape reveals a dynamic environment with increasing patent activity, emphasizing the importance of proactive portfolio management, diligent freedom-to-operate analyses, and strategic international filings.


Key Takeaways

  • The scope of CO2021015067 is primarily defined by its independent claims, emphasizing specific compounds or formulations.
  • Broad claims enhance market exclusivity but are more exposed to validity challenges; narrow claims offer defensibility at the expense of protection breadth.
  • Colombia’s patent landscape is evolving, with increasing filings and a focus on biologics and innovative delivery systems.
  • Strategic patent family expansion into regional and international markets amplifies protection and commercial opportunities.
  • Vigilance in claims drafting and patent prosecution is essential for leveraging Colombia's IP environment and safeguarding pharmaceutical innovations.

FAQs

1. What is the primary innovative element covered by Colombia patent CO2021015067?

The patent is granted for a specific pharmaceutical formulation, compound, or method, as detailed in its claims, which distinguish it from prior art—likely involving a novel therapeutic compound, delivery system, or combination therapy.

2. How broad are the claims typically in such pharmaceutical patents?

Claims can range from narrow, focusing on specific compounds or formulations, to broad, covering a class of compounds or methods. The scope depends on patent drafting strategy and prior art considerations.

3. Can this patent be extended or transferred internationally?

Yes. The patent family can extend via PCT applications or regional filings. The Colombian patent can be licensed, transferred, or used as a basis for international patent applications if the inventor or assignee pursues such strategies.

4. What are the main challenges in enforcing pharmaceutical patents in Colombia?

Enforcement challenges include opposition procedures, potential invalidity claims, and developing a jurisprudence supportive of patent rights. Accurate claim drafting and early strategic filings help mitigate these risks.

5. How does the Colombian patent landscape impact new drug development?

It encourages innovation by providing legal protection but requires careful navigation of existing patents. Effective IP management, including due diligence and strategic filings, informs R&D and commercialization pathways.


Sources:
[1] Colombian Superintendence of Industry and Commerce (SIC). Patent database and guidelines.
[2] World Intellectual Property Organization (WIPO). Patent landscape reports.
[3] Colombian Patent Law, Law 1450 of 2011.
[4] Industry reports on Colombian biomedical innovation trends.

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.