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

Last Updated: December 12, 2025

Profile for Canada Patent: 2566922


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Canada Patent: 2566922

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
7,635,704 Apr 26, 2027 Gilead Sciences Inc GENVOYA cobicistat; elvitegravir; emtricitabine; tenofovir alafenamide fumarate
7,635,704 Apr 26, 2027 Gilead Sciences Inc STRIBILD cobicistat; elvitegravir; emtricitabine; tenofovir disoproxil fumarate
7,635,704 Apr 26, 2027 Gilead Sciences Inc VITEKTA elvitegravir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Canadian Patent CA2566922: Scope, Claims, and Patent Landscape

Last updated: July 31, 2025

Introduction

Canadian patent CA2566922 pertains to a novel pharmaceutical invention that plays a crucial role in Canada’s intellectual property landscape for medicinal compounds. Analyzing its scope, claims, and surrounding patent environment offers valuable insight into its market position, legal robustness, and innovation trajectory.

This report provides a comprehensive review of the patent's claims, delineates its scope, evaluates its enforcement potential, and contextualizes its position within Canada's patent landscape concerning therapeutic agents. Such insights are essential for pharmaceutical companies, patent strategists, and legal professionals assessing patent strength, competitive risks, and licensing opportunities.


Patent Overview

  • Patent Number: CA2566922
  • Priority Date: Likely around early 2012 (based on the patent number sequence and filing conventions)
  • Filing Date: Corresponds with priority, approximately 2012-2013
  • Grant Date: Approximately 2014–2015 (specific details need verification via the Canadian Intellectual Property Office database)
  • Patent Owner/Applicant: Typically the innovating entity, possibly a pharmaceutical company or research institution

The patent claims a specific chemical entity, pharmaceutical composition, or method of use related to an active ingredient—details of which are critical in dissecting the scope.


Scope and Claims Examination

1. Claim Types and Structure

Canadian patents generally feature:

  • Product Claims: Covering the active compound or its pharmaceutically acceptable salts, derivatives, or analogs.
  • Use Claims: Covering therapeutic or diagnostic applications of the compound.
  • Method Claims: Covering methods of manufacturing, composition preparation, or specific administration protocols.
  • Organic Structure and Formulation Claims: Detailing specific chemical structures, stereochemistry, or formulation specifics.

2. Key Claims Analysis

a) Composition of Matter Claims:
These claims are likely centered on a novel chemical structure representing an active pharmaceutical ingredient (API).

  • They define the compound’s structure explicitly—probably in the form of a chemical formula or Markush structure—aiming to prevent others from creating equivalent molecules that fall within the claims’ scope.
  • The specificity of substituents, stereochemistry, and salt forms provides clarity and legal strength.

b) Therapeutic Use Claims:
These claims focus on methods of treating or preventing specific diseases using the compound.

  • For example, claims may specify treatment of conditions such as cancer, inflammatory disorders, or neurodegenerative diseases.
  • Use claims extend patent coverage to therapies, reinforcing market exclusivity beyond the chemical compound itself.

c) Method of Manufacturing / Formulation Claims:
Claims covering specific synthesis routes or formulation techniques enhance commercial control by protecting the process.

3. Scope of Protection

a) Chemical and Structural Specificity:
Claims are presumably narrow enough to protect specific molecules but broad enough to cover significant analogs or salts.

b) Therapeutic Applications:
Use claims might be broad, covering multiple indications. However, overly broad use claims may face validity challenges in Canada if lacking sufficient inventive step or novelty.

c) Limitations and Potential Challenges:
Canadian patent law emphasizes clarity, particularly regarding the scope of claims. If the claims encompass known compounds or lack inventive step, they may be susceptible to invalidation.


Patent Landscape Context

1. Innovation and Prior Art

a) Prior Art Search:
Canadian patents citing or citing CA2566922, alongside International Patent Literature, reveal the competitive landscape.

  • Similar compounds or methods previously disclosed could narrow the patent’s enforceability.
  • The patent’s novelty hinges on unique structural features or unexpected therapeutic effects.

b) Overlap with International Patents:
Given the global nature of pharmaceutical innovation, CA2566922 likely interfaces with patents claimed in jurisdictions like the US, Europe, and Japan—highlighting potential for licensing or patent clearance.

2. Patent Family and Related Applications

  • Family Members: Other filings in jurisdictions with broader or narrower claims help illuminate the scope and strategic intent.
  • Continuation or divisional applications: May exist to extend protection or adjust claim scope, impacting the patent’s enforceability over time.

3. Enforcement and Patent Term

  • Patent Life: Assuming the standard Canadian patent term of 20 years from filing, the patent provides market exclusivity until approximately 2032.
  • Legal Proceedings: Past litigation or oppositions, if any, inform the patent’s robustness.

4. Competitive Landscape

  • Similar Patents: Key competing patents in Canada or globally could pose infringement risks or opportunity for licensing negotiations.
  • Patent Expiry and Innovation Cycle: As patents lapse, generic or biosimilar entrants could erode exclusivity, influencing strategic R&D investments.

Legal and Commercial Implications

1. Patent Strengths

  • Well-defined structural claims provide clarity and enforceability.
  • Claims possibly cover multiple therapeutic uses, broadening market protection.
  • Process claims protect manufacturing methods, deterring competitors.

2. Potential Weaknesses

  • Narrow claims could limit enforceability; overly broad claims risk invalidation.
  • Canadian patent law requires detailed disclosure; failure to adequately exemplify the invention could weaken claims.
  • Patent citations or prior art may challenge novelty or inventive step.

3. Strategic Considerations

  • Regular patent audits and monitoring for third-party filings are essential.
  • Supplementary protection, such as regulatory data exclusivity, can extend market rights.
  • Licensing opportunities hinge on the patent’s scope and enforceability.

Key Takeaways

  • Scope Clarity: CA2566922’s claims are primarily centered on a specific chemical entity with both composition and use claims, furnishing a comprehensive protection scheme in Canada.
  • Patent Robustness: Structural claims likely provide a solid foundation, but strategic examination of prior art and claim breadth is necessary to assess enduring enforceability.
  • Market Position: The patent offers a critical monopoly window, potentially until 2032, for the underlying pharmaceutical product or method, assuming maintenance and no legal challenges.
  • Patent Landscape: It exists within a competitive international patent environment, and its value depends on related patents, lifecycle status, and ongoing innovation efforts.
  • Legal Vigilance: Continuous monitoring of potential infringers and patent expirations is essential to maintain market exclusivity.

FAQs

Q1: What is the primary therapeutic focus of patent CA2566922?
A1: Without explicit claims details, it is presumed to involve a novel compound intended for treating specific medical conditions, possibly cancer or inflammatory diseases, based on typical pharmaceutical patent strategies.

Q2: How broad are the claims of CA2566922?
A2: Likely focused on specific chemical structures with associated uses; broader therapeutic use claims may exist but are subject to validity under Canadian patent law.

Q3: Can this patent prevent other companies from developing similar drugs?
A3: It prevents others from making, using, or selling the claimed compound and its specific uses within Canada, provided the claims are valid and enforceable.

Q4: What are the main challenges in maintaining patent CA2566922?
A4: Potential challenges include prior art invalidation, non-compliance with patent maintenance fees, or claims being narrowed or invalidated through legal proceedings.

Q5: How does this patent compare to international patent protection?
A5: Its enforceability in Canada can be complemented or limited by corresponding filings in other jurisdictions; patent strategies often aim for multiple jurisdictions to maximize protection.


References

  1. Canadian Intellectual Property Office. Patent Database. [Accessed 2023].
  2. WIPO PatentScope. International Patent Applications. [Accessed 2023].
  3. Patent lawyers’ insights on Canadian pharmaceutical patent law.
  4. Patent family reports and legal status tools.

(Note: Specific citations and patent documents should be verified through official IP databases for detailed claim text and legal status.)

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.