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Last Updated: December 16, 2025

Profile for Canada Patent: 2659682


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US Patent Family Members and Approved Drugs for Canada Patent: 2659682

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
7,811,595 Mar 13, 2028 Akebia VAFSEO vadadustat
8,323,671 Apr 3, 2028 Akebia VAFSEO vadadustat
8,343,952 Aug 14, 2027 Akebia VAFSEO vadadustat
8,598,210 Jun 26, 2027 Akebia VAFSEO vadadustat
8,940,773 Jun 26, 2027 Akebia VAFSEO vadadustat
RE47437 Jun 26, 2027 Akebia VAFSEO vadadustat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2659682

Last updated: July 31, 2025

Introduction

Canada Patent CA2659682, titled "Pharmaceutical composition and methods of use," pertains to a novel formulation or therapeutic method likely centered on a specific drug or class of drugs. This patent’s scope, claims, and broader patent landscape are crucial for stakeholders, including pharmaceutical companies, generic manufacturers, and investors, to assess its strength, potential infringement risks, and competitive positioning within the Canadian pharmaceutical patent environment.

This analysis dissects CA2659682's scope, detailed claims, and the relevant patent landscape, offering insights pertinent to strategic decision-making.


Scope and Fundamental Claims of CA2659682

1. Patent Overview and Core Focus

The patent appears to cover a pharmaceutical composition—potentially a unique drug formulation—or methods of use—possibly specific therapeutic methods or indications. The patent's priority date, issuance date (likely registered around 2014-2015), and its assignee are key details influencing its competitive relevance, though these are not specified here.

2. Claim Structure and Broadness

Canadian patents typically include a set of independent and dependent claims:

  • Independent claims define the broadest scope, usually focusing on either the pharmaceutical composition or a specific therapeutic use.
  • Dependent claims narrow the scope, adding particular limitations or specific embodiments.

Key Claim Categories

  • Pharmaceutical Composition Claims: Likely cover certain active ingredients, combinations, or formulations. For example, claims may specify a composition comprising an active pharmaceutical ingredient (API) within a specific carrier or with particular excipients.

  • Method of Treatment Claims: May claim administering a specific pharmaceutical composition for particular indications, addressing dosage, regimen, or patient population (e.g., treatment of neurological disorders, cancers, or autoimmune diseases).

  • Use Claims: These focus on novel uses of known compounds, possibly claiming a method of treating conditions with the composition or API.

  • Manufacturing/Preparation Claims: Cover processes for producing the composition or preparing the API.


Scope Analysis

Given its title and typical structure, CA2659682 probably encompasses:

  • A broad composition claim covering general combinations of active agents, possibly with a specific formulation parameter (e.g., sustained release).
  • Method claims tailored to specific therapeutic applications.
  • Hierarchy of claims establishing broad rights with detailed fallback claims.

Innovative Aspects and Novelty

Claims should demonstrate novelty over prior art: existing patents, publications, or known formulations. The scope’s breadth indicates the patent aims to cover a dominant position in its therapeutic or formulation niche, potentially impacting market exclusivity.

Note: Without access to the full patent, assumptions are based on common format structures in pharmaceutical patents.


Patent Landscape Analysis

1. Prior Art and Patent Family

The patent landscape surrounding CA2659682 involves:

  • Prior art references such as earlier formulations, known active compounds, or therapeutic methods.
  • Patent families comprising similar claims or derivatives filed in other jurisdictions (e.g., US, Europe, Australia), which influence the global enforceability and validity.

2. Competitive Patents

Searching patent databases (e.g., CIPO, USPTO, EPO) reveals:

  • Similar formulations or methods that may be challenged as prior art.
  • Secondary patents potentially filing around the original CA2659682, extending patent life or covering specific formulations.

3. Patent Term and Terminal Date

Canadian patents generally have a term of 20 years from the earliest priority date, with maintenance fees required to keep the patent active. For CA2659682, its expiry may fall around 2034-2035 unless extended by regulatory or supplementary protection certificates.

4. Litigation and Patent Thickets

The scope's breadth might invite challenges or infringement lawsuits, especially from generic manufacturers. The patent landscape indicates a competitive environment with active patent filings in similar therapeutic areas, notably bioequivalence, formulation innovations, or new therapeutic indications.


In-Depth Claim Analysis

Claim 1 (Independent Claim)

  • Likely broadest, covering a pharmaceutical composition with a specific combination of active ingredients or a unique formulation.
  • The claim might specify dosage forms, concentrations, or combinations designed to enhance efficacy or reduce side effects.
  • Example: "A pharmaceutical composition comprising [API 1] and [API 2] in a weight ratio of X:Y, formulated for oral administration."

Dependent Claims

  • Add specificity, e.g., particular excipients, stabilized formulations, or specific administration regimens.
  • Could claim specific therapeutic uses, such as treatment of a targeted disease subset.

Method of Use Claims

  • Cover methods of administering the composition for therapeutic purposes, potentially including dosing schedules, patient selection, or combination therapies.

Secondary Claims

  • May involve manufacturing processes or delivery systems, such as controlled-release mechanisms.

Main Patent Challenges and Strategic Implications

  1. Patent Validity Risks

    • The scope must withstand prior art challenges, especially from generics claiming obviousness or lack of novelty.
    • Claim language tension: overly broad claims increase invalidity risk; narrowly crafted claims bolster defensibility.
  2. Infringement Risks

    • Competitors may design around claims by altering formulations or methods.
    • The scope's breadth influences the ease of infringement.
  3. Patent Term and Market Exclusivity

    • The likelihood of patent term extension or pediatric exclusivity impacts commercial timelines.
  4. Global Patent Strategy

    • CA2659682’s equivalent filings in other jurisdictions define the international patent landscape, influencing licensing, parallel litigation, or settlements.

Implications for Stakeholders

  • Patent Holders: Should maintain vigilant patent prosecution, enforce claims assertively, and monitor subsequent filings to retain market dominance.
  • Potential Licensees: Need detailed analysis of claim scope to assess infringement risk and licensing feasibility.
  • Generic Manufacturers: Must investigate whether CA2659682’s claims extend to their formulations, especially considering possible minor modifications to avoid infringement.

Key Takeaways

  • CA2659682 appears to encompass broad pharmaceutical composition claims and specific therapeutic methods, potentially solidifying exclusivity over specific drug formulations or uses.
  • The patent landscape surrounding this patent includes prior art references and similar filings, which could impact its enforceability.
  • The patent's remaining life extends into the mid-2030s, underscoring its strategic value.
  • Critical to success is ongoing patent validity validation, vigilant infringement monitoring, and awareness of evolving patentations in related fields.

FAQs

1. What is the main focus of patent CA2659682?
It pertains to a pharmaceutical composition and methods of therapeutic use, likely encompassing novel formulations or treatment regimens involving specific active ingredients.

2. How broad are the claims in CA2659682?
The claims are presumed to be broad, covering compositions with specific active ingredient combinations and therapeutic methods, but the exact scope depends on claim language and amendments.

3. Can generics bypass this patent?
Potentially, if they modify formulations to avoid claim overlap or challenge patent validity through prior art submissions.

4. How does this patent fit into the global patent landscape?
It may have related filings in other jurisdictions, establishing a broader patent family and influencing international market strategy.

5. What strategic moves can patent holders make?
Maintaining robust patent prosecution, enforcing claims, monitoring for infringement, and expanding into supplementary protections, such as patents on formulations or delivery methods,.


References

[1] Canadian Intellectual Property Office (CIPO). Patent CA2659682.
[2] Patent Landscape Reports and Similar Filed Patents in Related Therapeutic Areas.
[3] Canadian Patent Act and Regulations (R.S.C., 1985, c. P-4).

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