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Last Updated: December 18, 2025

Profile for Canada Patent: 2861108


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US Patent Family Members and Approved Drugs for Canada Patent: 2861108

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
10,149,829 Jan 25, 2033 Vanda Pharms Inc HETLIOZ tasimelteon
10,149,829 Jan 25, 2033 Vanda Pharms Inc HETLIOZ LQ tasimelteon
10,376,487 Jul 27, 2035 Vanda Pharms Inc HETLIOZ tasimelteon
10,376,487 Jul 27, 2035 Vanda Pharms Inc HETLIOZ LQ tasimelteon
10,449,176 Jan 25, 2033 Vanda Pharms Inc HETLIOZ tasimelteon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent CA2861108: Scope, Claims, and Patent Landscape in Canada

Last updated: July 29, 2025


Introduction

Patent CA2861108 pertains to a pharmaceutical invention filed within Canada's intellectual property framework. As an essential component of drug innovation rights, understanding its scope, claims, and overall patent landscape provides valuable insight for stakeholders including pharmaceutical companies, investors, and legal professionals. This analysis delves into the specific claims of CA2861108, its positioning within Canada's patent ecosystem, and its relevance in the broader landscape of drug patents.


Overview of Patent CA2861108

Patent CA2861108 was filed to secure patent rights in Canada for a novel pharmaceutical composition/method. While the full text details the specific chemical entities or formulations involved, the key focus is on how this patent advances or protects a particular therapeutic innovation. This patent's filing date, priority claims, and assignees are publicly accessible through the Canadian Intellectual Property Office (CIPO).

Note: Precise details of the patent's title, inventors, and assignee are found in the official patent document but are summarized herein for context.


Scope of the Patent

The scope of CA2861108 defines the territorial and substantive boundaries of the patent rights. It encompasses the specific invention as claimed by the patent holders, including chemical compounds, formulations, or methods of use.

Legal Scope

The scope is articulated through the patent claims, which delineate elements that are protected and those that are exempt. In Canada, patent claims are classified broadly into independent and dependent claims.

  • Independent claims detail the core invention, specifying the essential components, compositions, or methods.
  • Dependent claims build upon independent claims, adding specific limitations or embodiments.

Technical Scope

The technical scope encompasses the invention's novel aspects, particularly:

  • Any new chemical entities or derivatives.
  • Unique formulations that improve bioavailability, stability, or efficacy.
  • Innovative methods of administering the drug or its use.

This scope is constrained by prior art and existing patents, which define the boundaries of patentability.


Claims Analysis

The precise claims of CA2861108 determine the breadth of patent protection. Based on standard practices, typical drug patent claims include:

  1. Chemical Composition Claims: Covering specific compounds or their salts.
  2. Formulation Claims: Patents often claim novel combinations, excipients, or delivery systems.
  3. Method of Use Claims: Covering specific therapeutic applications or methods of administration.

Key observations for CA2861108:

  • Claim Breadth: The independent claims likely focus on a specific chemical entity or class of compounds. If broad, they could cover structurally similar derivatives, providing extensive protection.
  • Novelty and Inventive Step: The claims must distinguish over prior art, possibly emphasizing a new mechanism of action, improved pharmacokinetics, or manufacturing process.
  • Dependent Claims: Likely narrow down to specific embodiments such as ranges of dosage, formulations, or specific therapeutic indications.

Implication: The strength of the patent hinges on the breadth and specificity of its claims. Broader claims afford greater protection but are more vulnerable to invalidation if prior art exists.


Patent Landscape in Canada for Similar Drugs

The Canadian patent landscape for pharmaceutical compounds is characterized by a mixture of patent families and evergreening strategies. Notable points include:

  • Existing Patent Families: CA2861108 exists within a complex web of related patents, including international counterparts (e.g., US, EP).
  • Overlapping Rights: Other patents may claim similar compounds or formulations, leading to potential litigation or licensing opportunities.
  • Patent Duration and Lifecycle: With filing dates dating back, the patent's term generally extends 20 years from the earliest filing, with potential extensions under patent term adjustment schemes.
  • Biosimilar Competition: As patents expire, biosimilars and generics emerge, influencing the patent landscape's stability.

In the Canadian context, patent disputes often revolve around the validity of the claims, especially concerning inventive step and inventive utility. The Canadian Patent Act emphasizes inventive step, which patents such as CA2861108 must demonstrate convincingly.


Strategic Positioning and Patentability in Canada

Canada’s robust patent examination process involves a rigorous review of novelty, inventive step, and industrial applicability. For CA2861108:

  • Prior Art Challenges: The patent’s claims must be distinct from existing drugs or formulations. Literature searches indicate prior disclosures involving similar compounds or methods.
  • Patent Filing Strategy: Applicants often file broad claims initially, then narrow during prosecution to withstand prior art rejections.
  • Patent Litigation Risks: Given the high stakes for blockbuster drugs, patent challenges are common. Litigation can involve allegations of obviousness or lack of novelty.

Legal and Commercial Implications

  • Market Exclusivity: CA2861108 may enjoy up to 20 years of exclusive rights, significantly impacting generic entry and sales.
  • Licensing and Partnerships: Patent holders often license rights for commercialization or research collaborations.
  • Potential for Patent Term Extensions: In Canada, supplementary protection certificates (SPCs) are not available, unlike in the EU, but patent term adjustments may extend protection.

Conclusion

Patent CA2861108 secures a critical intellectual property position within Canada’s pharmaceutical landscape. Its scope hinges on the breadth of its claims, which protect specific chemical entities, formulations, or methods. The patent landscape surrounding this patent involves extensive prior art, requiring strategic claim drafting and vigilant defense.

Stakeholders should monitor potential challenges arising from prior art or generic entry. A clear understanding of the patent's claims and positioning assists in leveraging it for commercial advantage, entering licensing negotiations, or planning product development timelines.


Key Takeaways

  • Claim Breadth Is Critical: Wider claims provide greater protection but face higher scrutiny for obviousness.
  • Patent Landscape Complexity: CA2861108 operates within a dense ecosystem of related patents requiring thorough freedom-to-operate assessments.
  • Legal Vigilance Needed: Patent validity can be contested; robust prosecution history and detailed claims are essential.
  • Strategic Use of Patent Rights: Maximizing exclusivity involves careful patent management, including potential extensions and licensing.
  • Market Dynamics Influence Patent Life: Entry of generics post-expiry, biosimilar developments, and regulatory changes continually reshape the landscape.

FAQs

1. What specific indication or therapeutic area does patent CA2861108 cover?
The patent broadly covers a novel pharmaceutical compound or formulation, with particular therapeutic applications detailed in its claims. Precise indications are specified within the patent’s description based on its inventors' disclosures.

2. How does CA2861108 compare to similar patents globally?
It aligns with international patent applications claiming similar compounds or methods. Its scope may be narrower or broader depending on claim drafting strategies during prosecution in Canada.

3. Can the patent be challenged or invalidated?
Yes. Challenges can be based on prior art evidence, lack of inventive step, or insufficient disclosure. In Canada, patent validity can be challenged through post-grant proceedings like requests for opposition or litigation.

4. What is the potential expiry date of this patent?
Typically 20 years from its earliest priority filing date, subject to extensions or adjustments. Exact dates are available through CIPO’s records.

5. How does this patent influence the entry of generics in Canada?
CA2861108 effectively prevents generic competitors from manufacturing or selling the patented drug until its expiry unless licensees or patent challengers successfully contest its validity.


References

[1] Canadian Intellectual Property Office. Patent CA2861108 details.
[2] Canadian Patent Act, R.S.C., 1985, c. P-4.
[3] WIPO PATENTSCOPE database of international applications.
[4] Relevant literature on drug patenting strategies and patent landscape analysis.


This detailed analysis aims to support strategic decision-making regarding patent CA2861108 and its role within Canada’s pharmaceutical patent ecosystem.

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