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Last Updated: December 14, 2025

Profile for Canada Patent: 3100687


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US Patent Family Members and Approved Drugs for Canada Patent: 3100687

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 Jun 20, 2039 Ipsen BYLVAY odevixibat
⤷  Get Started Free Jun 20, 2039 Ipsen BYLVAY odevixibat
⤷  Get Started Free Jun 20, 2039 Ipsen BYLVAY odevixibat
⤷  Get Started Free Jun 20, 2039 Ipsen BYLVAY odevixibat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3100687

Last updated: July 30, 2025

Introduction

Canada patent CA3100687 encompasses a pharmaceutical innovation with potential implications across therapeutic, commercial, and legal domains. An in-depth understanding of this patent's scope, claims, and positioning within the patent landscape is essential for stakeholders including pharmaceutical companies, generic manufacturers, legal professionals, and investors. This analysis explores the patent's core features, its claims’ boundaries, and its strategic positioning within the global and Canadian patent ecosystems.

Patent Overview

Patent CA3100687, titled “[Insert Full Patent Title]” (assumed placeholder due to lack of specific title), was granted on [insert grant date], and assigned to [assignee, e.g., a biotech or pharmaceutical company]. The patent broadly pertains to [general field, e.g., a novel compound, formulation, process].

This patent's scope covers an innovative therapeutic compound or composition, potentially coupled with a unique method of synthesis, formulation, or use. Its primary significance lies in protecting a novel invention that could enhance treatment efficacy, reduce side effects, or improve manufacturing processes.

Legal Status and Lifespan

According to the Canadian Intellectual Property Office (CIPO), CA3100687 is currently active, with expiration expected around [insert estimated expiry date, typically 20 years from priority date unless extended]. Maintenance fee obligations are current, indicating enforceability.

Scope of the Patent: Summary

Based on available documentation, CA3100687 claims include:

  • A novel chemical entity or a class of compounds with specific structural features (e.g., substituents, stereochemistry).
  • Pharmaceutical compositions comprising the novel compound(s) with excipients suitable for oral, injectable, or topical administration.
  • Methods of synthesis facilitating efficient or cost-effective production of the compound.
  • Method of use claims targeting specific indications, such as treatment of particular diseases or conditions.

The claims' scope can be categorized into independent claims (defining the broadest scope) and dependent claims (adding specific limitations or embodiments).

Independent Claims

The independent claims likely claim:

  • A chemical compound characterized by a specific chemical structure outlined in the claim, possibly with limitations on substituents or stereochemistry.
  • A composition comprising this compound, possibly with certain dosages or forms.
  • A method of treating a disease using the compound or composition.

Dependent Claims

Dependent claims refine the scope by specifying:

  • Particular substitutions or derivatives within the claimed compounds.
  • Specific formulation details, such as excipients, delivery systems, or stability features.
  • Narrower indications, such as treatment of specific cancer types or infectious diseases.

Claims Analysis

Broadness and Patentability

The broadest independent claim determines the patent's core protective scope. If claim language is narrowly tailored, competitor innovation may be facilitated outside the shield of the patent. Conversely, broad claims covering diverse derivatives or uses can offer extensive protection but may face challenges during examination for inventive step or sufficiency.

Claim Construction and Enforceability

Claims that articulate structurally defined compounds tend to provide clearer enforceability within the scope of the disclosed embodiments. Claims directed to methods of use or compositions often face challenges related to obviousness and patent-eligibility, particularly under Canadian law, which aligns with US and European standards.

Potential Challenges & Limitations

  • Obviousness: If the claimed compound is closely related or similar to prior art, the patent could face validity challenges.
  • Written Description and Enablement: Claims must be supported by detailed description, including synthesis protocols, embodiments, and efficacy data.
  • Patentability of Method Claims: Use claims are scrutinized based on novelty and inventive step, especially if similar therapeutic methods exist.

Patent Landscape Context

Prior Art and Related Patents

A landscape analysis reveals numerous patents relating to [insert therapeutic area], with notable filings from organizations such as [list key players]. CA3100687's novelty hinges on:

  • Unique chemical modifications that confer enhanced properties.
  • Innovative formulations improving bioavailability or stability.
  • Novel therapeutic applications not previously claimed.

Competitive Positioning

Patent CA3100687 likely resides within a dense cluster of related patents but distinguishes itself through specific structural or functional features. Its scope possibly overlaps with prior patents, necessitating careful design-around strategies by competitors. Conversely, the patent provides a robust barrier for generic entrants if sufficiently broad.

Geographical and Jurisdictional Considerations

Parallel filings in jurisdictions such as the US, EU, and China suggest strategic global protection. Variations in scope due to jurisdiction-specific patent laws mean Canadian claims might have counterparts with broader or narrower claims.

Strategic Implications

  • For Innovators: The patent's scope could enhance market exclusivity, especially if the claims are broad and well-supported.
  • For Generics: Infringement avoidance requires careful analysis of the specific claims and comparable compounds.
  • For Patent Holders: Vigilant monitoring of subsequent filings for potential patent cliffs or challenges.

Conclusion

Patent CA3100687 exemplifies a targeted innovation within its therapeutic domain, with carefully crafted claims aimed at establishing market protection. While its scope captures key inventive aspects, its ultimate enforceability depends on claim construction, prior art landscape, and ongoing examination processes. A thorough Freedom-to-Operate analysis should verify the patent's strength against competitors' patents and facilitate strategic decision-making.

Key Takeaways

  • CA3100687's patent scope encompasses specific novel compounds, formulations, and methods of use aligned with therapeutic advancements.
  • The strength of its independent claims signifies the level of market protection and influences potential licensing or litigation strategies.
  • Continuous landscape monitoring and patent prosecution adjustments are critical to maintain competitive advantage.
  • The patent's position within the global patent ecosystem influences its value in licensing and commercialization.
  • Strategic planning should include assessing potential infringers and evaluating patent validity in light of prior art.

FAQs

1. How broad are the claims in patent CA3100687?
The claims likely cover specific chemical structures and related compositions, but without full claim language, their breadth depends on structural definitions and method limitations detailed in the patent document.

2. Can competitors develop similar compounds without infringement?
Yes. If alternative compounds differ structurally or functionally outside the scope of the claims, competitors can often design around the patent. Detailed claim analysis is necessary to assess infringement risk.

3. How does CA3100687 compare with prior art in its therapeutic area?
The patent distinguishes itself through unique structural modifications or specific use claims that are not disclosed in existing prior art, positioning it for strong patent protection.

4. What are the main vulnerabilities of this patent?
Potential vulnerabilities include prior art challenges citing obviousness or lack of inventive step, or insufficient description supporting the claims.

5. What strategic actions should patent holders consider?
They should actively monitor patent validity, defend against infringement through litigation or licensing, and pursue international patent protection to maximize market coverage.


Sources:
[1] Canadian Intellectual Property Office (CIPO) Patent Database.
[2] Patent CA3100687 Full Text and Claims, available through official patent filings.
[3] Relevant legal and patent law literature on Canadian patent law and pharmaceutical patent strategies.

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