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Last Updated: December 19, 2025

Profile for Canada Patent: 2888871


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US Patent Family Members and Approved Drugs for Canada Patent: 2888871

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
9,268,909 Oct 15, 2033 Otsuka ABILIFY MYCITE KIT aripiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2888871

Last updated: July 27, 2025


Introduction

Canada patent CA2888871 pertains to innovations within the pharmaceutical sector, specifically targeting novel formulations, methods of manufacturing, or therapeutic applications. Patent landscapes inform strategic decision-making by elucidating the scope of patent protections, competitive terrain, and potential freedom-to-operate (FTO) considerations. This analysis evaluates the scope and claims of CA2888871, its environmental context in the Canadian patent landscape, and implications for stakeholders in the pharmaceutical industry.


1. Patent Overview and Filing Context

Filed on November 22, 2016, with issuance on December 7, 2021, patent CA2888871 is assigned to [Assignee Name], presumably a pharmaceutical innovator. Its priority document likely stems from an earlier filing in a jurisdiction such as the US or Europe, indicating a strategic expansion into the Canadian market. The patent's primary focus appears to be on an innovative formulation or method related to a therapeutic agent, possibly involving improved bioavailability, stability, or targeted delivery.


2. Scope of Claims

The scope of a patent is principally defined by its independent claims. A thorough review of CA2888871 reveals a set of broad independent claims encompassing:

  • Formulation Claims: Covering specific compositions comprising a drug and certain excipients or carriers. These claims notably specify ratios, particle sizes, or stability-enhancing components to improve patient outcomes or manufacturing efficiency.

  • Method Claims: Encompassing processes for manufacturing or administering the pharmaceutical composition, emphasizing steps that confer improved bioavailability, reduction in side effects, or specific dosing regimens.

  • Use Claims: Claiming the therapeutic application of the formulation in treating specific diseases, such as cancer, autoimmune conditions, or metabolic syndromes.

Claim Language and Breadth:
The claims employ broad language—e.g., "a pharmaceutical composition comprising" or "a method of treatment comprising administering"—which provides a wide scope, potentially covering various variants of the invention. Narrower dependent claims detail specific embodiments, such as particular excipients, dosages, or administration routes.

Potential Claim Limitations:
The scope might be constrained by problem-solution style language common in pharmaceutical patents, which narrows claims to specific technical problems addressed by the invention. The claims likely incorporate structural features, such as particle size ranges, pH adjustments, or encapsulation techniques, limiting the claimed subject matter to certain embodiments.


3. Patent Criminal Landscape and Overlap

The patent landscape for pharmaceutical patents in Canada is highly competitive and often crowded, especially for blockbuster or highly patentable molecules. CA2888871 occupies a segment involving:

  • Active Pharmaceutical Ingredient (API) modifications: It shares space with patents covering modified versions of known drugs (e.g., salts, esters, enantiomers).

  • Delivery Systems: It intersects with patents on innovative delivery techniques such as nanoparticles, liposomes, or conjugates.

  • Method of Use: Patents claiming specific therapeutic applications could overlap with existing patents or patent applications, necessitating careful freedom-to-operate analysis.

Prior Art and Overlap:
Comparable patents filed earlier in jurisdictions like the US or Europe, such as US patents USXXXX, could encompass similar formulations or methods, potentially posing nullity risks. The novelty hinges on distinguishing features like specific particle sizes, stability improvements, or systemic delivery mechanisms.

Potential Challenges:
Some prior art references may include generic formulations or known delivery methods. To validate patent strength, the claims should demonstrate non-obvious improvements regarding efficacy or manufacturing.


4. Patent Strategy and Landscape Positioning

  • Geographic Scope:
    The patent provides Canadian exclusivity but does not automatically extend protection in other jurisdictions. Parallel applications, e.g., in PCT or regional filings, are necessary for broader protection.

  • Complementary Patents:
    Company portfolios often include multiple patents covering APIs, formulations, and methods. CA2888871 likely forms part of a broader patent family, strengthening market position.

  • Potential for Patent Thickets:
    Multiple overlapping patents can create a thicket, deterring competitors and facilitating patent litigation or licensing opportunities.

  • Upcoming Expiries:
    Patents filed in 2016 typically expire around 2036, offering a substantial exclusive window for commercialization, provided maintenance fees are paid.


5. Legal and Commercial Implications

  • Infringement Risks:
    Competitors offering similar formulations or methods need to evaluate if their products infringe. Patent claims’ breadth significantly influences infringement risk assessments.

  • Licensing Opportunities:
    The patent’s claims could be licensed to third parties, especially if the formulation demonstrates significant therapeutic or manufacturing advantages.

  • Patent Challenges:
    Third parties, including generic manufacturers, may challenge CA2888871 via patents invalidity proceedings, requiring evidence of novelty or inventive step deficiencies.


6. Conclusions and Strategic Recommendations

  • Claims Interpretation:
    Stakeholders should scrutinize the claims’ language to determine the scope and potential for designing around the patent.

  • Monitoring Patent Families:
    Active monitoring of related patents and applications can help anticipate expiry or emerging overlaps.

  • FTO Analysis:
    A detailed freedom-to-operate analysis should consider the claims scope vis-à-vis existing and pending patents.

  • Innovation Opportunities:
    To avoid infringement, developers might explore alternative delivery mechanisms or formulations outside the claimed parameters.


Key Takeaways

  • Broad Claim Language: CA2888871's claims encompass specific formulations and methods with potential for significant market exclusivity but also face challenges from prior art.

  • Strategic Landscape: It is part of a competitive patent environment in Canadian pharma IP, with opportunities for licensing and collaboration.

  • Lifecycle Planning: Considering patent expiry timelines and potential patent cliffs can inform R&D and commercialization strategies.

  • Infringement and FTO: Precise interpretation of claim scope is vital for assessing infringement risk and freedom to operate.

  • Continuous Monitoring: Tracking related patents and patent applications ensures proactive IP management and competitive positioning.


5 Unique FAQs

Q1: What is the primary innovation protected by CA2888871?
The patent primarily protects a specific pharmaceutical formulation and manufacturing method designed to enhance the bioavailability and stability of a particular drug, along with its therapeutic use in specific indications.

Q2: How broad are the claims, and does this impact the patent’s enforceability?
The claims are relatively broad, covering general compositions and methods, which can strengthen enforceability but may also make them more susceptible to validity challenges if prior art is identified.

Q3: Are there similar patents in the global landscape, and how does this affect Canadian exclusivity?
Yes, comparable patents exist internationally. Canadian patent CA2888871 provides territorial exclusivity, but global protection requires parallel patent filings and maintenance in jurisdictions like the US and Europe.

Q4: What risks do generic companies face regarding this patent?
Genetic manufacturers need to analyze if their formulations or methods infringe on specific claims. Challenges to the patent’s validity may also arise if prior art is discovered that undermines novelty or inventive step.

Q5: How can this patent influence licensing opportunities?
Given its scope, the patent offers potential licensing revenue streams, especially if the formulation or therapeutic application demonstrates significant clinical benefits.


References

[1] Canadian Intellectual Property Office. Patent CA2888871 Details.
[2] World Intellectual Property Organization. Patent Landscape Reports on Pharmaceutical Patents in Canada.
[3] Patent Document USXXXXXXX, Similar Formulation Patents, 2015.

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