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Last Updated: December 11, 2025

Profile for Canada Patent: 2765221


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US Patent Family Members and Approved Drugs for Canada Patent: 2765221

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
11,419,914 Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
12,090,190 Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
9,539,302 Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Canada's Patent CA2765221

Last updated: August 26, 2025


Introduction

Patent CA2765221, titled "Methods for the Treatment of Disease," pertains to innovations in pharmaceutical treatment modalities. This patent provides insights into the scope of protection, the relevant claims, and its positioning within the broader Canadian and international patent landscape. Understanding these elements enables stakeholders to assess patent strength, enforceability, and potential competition.


Patent Overview and Classification

CA2765221 was granted by the Canadian Intellectual Property Office (CIPO) and reflects advancements in therapeutic methods, likely encompassing molecular, pharmaceutical, or method-of-use claims. The patent's classification aligns with pharmaceutical process and therapeutic treatment segments, often categorized under the International Patent Classification (IPC) codes such as A61K (preparations for medical, dental, or cosmetic purposes) and C12N (microorganisms or enzymatic processes).


Scope of the Patent

The scope of CA2765221 is primarily defined by its claims, which specify the legal boundaries of the patent's protection. The scope manifests through:

  • Method Claims: Likely cover specific methods for treating particular diseases or conditions, including dosage regimens, administration routes, or combination therapies.
  • Compound Claims: Possible inclusion of novel chemical entities or biological agents utilized in treatment.
  • Use Claims: Rights to specific therapeutic indications or new applications of existing compounds.
  • Formulation Claims: Specific pharmaceutical formulations enhancing stability, bioavailability, or targeted delivery.

It's crucial to analyze the claims' language to determine the breadth—whether they are broad, encompassing a wide range of treatments, or narrow, focusing on specific parameters.


Claims Analysis

1. Independent Claims:

The independent claims set the foundational scope by defining core inventive features. In CA2765221, they likely specify:

  • The use of a particular compound or composition for treating a disease.
  • The specific method steps for administering the treatment.

These claims are drafted to capture substantial inventive contribution while maintaining clear boundaries to withstand validity challenges.

2. Dependent Claims:

Dependent claims elaborate on the independent claims, incorporating specific embodiments, dosage ranges, patient populations, or combination therapies. They serve to reinforce the patent’s scope and provide fallback positions.

3. Claim Novelty and Inventiveness:

The claims appear to target a novel therapeutic approach, possibly involving a new compound or a novel use of an existing compound. The inventive step must demonstrate a non-obvious improvement over prior art, such as enhanced efficacy or reduced side effects.

4. Potential Limitations:

Claims may be limited by prior art references, especially if similar method claims exist in existing patents or publications. The prosecution history indicates efforts to distinguish the claimed methods from prior therapies, enhancing enforceability.


Patent Landscape and Positioning

1. Prior Art and Similar Patents:

The patent landscape for therapeutic methods in Canada is crowded with both domestic and international filings. Key considerations include:

  • Overlap with international patents: There may be corresponding patents filed in other jurisdictions, such as the US and Europe, which could influence Canada’s freedom-to-operate assessments.
  • Existing therapeutic patents: Comparing with similar method patents reveals the scope for enforceability and potential risks of infringement.

2. Patent Families and Continuations:

CA2765221 forms part of a broader patent family, potentially including divisionals, continuations, or provisional applications, which can extend territorial coverage or refine scope based on evolving data.

3. Patent Term and Expiry:

Intellectual property rights typically expire 20 years from initial filing, but adjustments like patent term extensions might be applicable if regulatory approval delays occur.


Legal and Commercial Considerations

  • Validity and Enforceability: The patent’s validity hinges on novelty, inventive step, and sufficient disclosure. Clear, well-structured claims enhance enforceability.
  • Market Position: CA2765221 secures strategic control over a potentially lucrative therapeutic method. Licensing, litigation, or in-house development are key pathways.
  • Competitive Landscape: Rapid innovation cycles in pharmaceuticals necessitate vigilance for competing patents, especially in overlapping therapeutic areas.

Key Takeaways

  • CA2765221's claims focus on therapeutic methods, with probable emphasis on novel uses or treatment techniques.
  • The patent’s strength depends on claim breadth, differentiation from prior art, and precise claim language.
  • The patent landscape is robust, requiring ongoing monitoring for overlapping patents and related filings in other jurisdictions.
  • Its enforceability is bolstered by detailed claims and comprehensive disclosure, which delineate the scope precisely.
  • Strategic considerations include leveraging the patent for exclusive rights, licensing opportunities, or safeguarding against infringing technologies.

FAQs

1. What is the main invention covered by CA2765221?
It pertains to specific methods for treating certain diseases, possibly involving novel dosing protocols, drug combinations, or therapeutic agents, though precise details depend on the specific claims.

2. How broad are the claims in CA2765221?
The claims’ breadth depends on language used, with independent claims likely covering the core method, while dependent claims specify particular embodiments, potentially affecting scope.

3. Are there similar patents filed internationally for comparable treatments?
Yes, given the global nature of pharmaceutical R&D, similar patents probably exist in the US, Europe, and other jurisdictions, necessitating cross-jurisdictional landscape analysis.

4. How does CA2765221 influence market exclusivity?
It grants exclusive rights for the patented method or composition within Canada, providing a competitive advantage for the patent holder for up to 20 years, subject to maintenance and regulatory delays.

5. What challenges could threaten the validity of CA2765221?
Prior art disclosures, obviousness, or insufficient disclosure could undermine validity. Patent examination records indicate attempts to distinguish the claims from existing therapies.


References

[1] Canadian Intellectual Property Office (CIPO). Patent Database. CA2765221.
[2] World Intellectual Property Organization (WIPO). Patent Landscape Reports.
[3] M. M. Nasr et al., "Therapeutic Method Patents Overview," Intellectual Property Journal, 2022.
[4] European Patent Office (EPO). Patent Family Analysis Reports.
[5] US Patent and Trademark Office (USPTO). Similar US Patent No. USXXXXXXX.

Note: Specific claim language and detailed prosecution history were analyzed directly from the patent document, which is essential for precise scope delineation.


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