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Last Updated: December 12, 2025

Profile for Canada Patent: 2777857


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US Patent Family Members and Approved Drugs for Canada Patent: 2777857

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
9,308,204 Oct 21, 2030 Msd Sub Merck SEGLUROMET ertugliflozin; metformin hydrochloride
9,308,204 Oct 21, 2030 Msd Sub Merck STEGLUJAN ertugliflozin; sitagliptin phosphate
9,439,901 Oct 21, 2030 Msd Sub Merck STEGLUJAN ertugliflozin; sitagliptin phosphate
9,439,902 Oct 21, 2030 Msd Sub Merck SEGLUROMET ertugliflozin; metformin hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2777857

Last updated: July 31, 2025


Introduction

Patent CA2777857, granted by the Canadian Intellectual Property Office (CIPO), encompasses innovations related to a novel therapeutic compound or formulation relevant to the pharmaceutical industry. This analysis offers a comprehensive assessment of its scope, claims, and positioning within the broader patent landscape, aimed at informing stakeholders including biotech firms, generic manufacturers, and legal professionals.


Patent Overview and Basic Information

Patent Number: CA2777857
Filing Date: (Assumed based on typical patent lifecycle; for precise details, consult CIPO records)
Grant Date: (Assumed)
Assignee: (Likely a pharmaceutical company or research institution, specifics depend on patent records)
Patent Classification: Likely falls under classes related to pharmaceuticals, chemical compositions, or drug delivery systems, e.g., CPC class A61K for medicinal preparations.


Scope of the Patent

The core of CA2777857 resides in its claims, which define the legal scope of protection. The patent appears to focus on:

  • Chemical Formulations: Specific chemical entities, including compounds or their derivatives with therapeutic activity.
  • Innovative Use: Novel applications of known compounds for particular medical conditions.
  • Manufacturing Methods: Processes for synthesizing the claimed compounds.
  • Delivery Systems: Unique formulations or delivery mechanisms enhancing bioavailability or stability.

The patent likely asserts protection over a class of compounds with specific structural features, possibly including specific substituents or stereochemistry critical for activity. It may also claim related methods, such as dosing protocols or combination therapies.


Claims Analysis

The patent's claims can be broadly segmented into two categories:

1. Composition of Matter Claims

These are the primary claims and define the protected chemical entities. Typically, such claims specify:

  • The chemical structure of the compound(s), often through Markush groups to encompass a range of derivatives.
  • Specific substituents or stereochemistry that confer therapeutic advantages.
  • Purity levels or formulations.

Example: A claim might state: "A compound of formula I, wherein R1 and R2 are independently selected from hydrogen, alkyl, or halogen, exhibiting activity against [target disease]."

2. Method Claims

Cover methods of:

  • Synthesizing the compounds.
  • Using the compounds for treating a disease.
  • Administering the compounds via specific routes or delivery systems.

Scope of Method Claims: These may be more narrow but provide additional protection for the therapeutic use, especially if composition claims face challenges.

Claim Construction and Limitations

  • The scope hinges on the breadth of the chemical structures claimed. Broad claims provide extensive protection but can be challenged for patentability.
  • Narrow claims centered on specific compounds or methods may face less infringement risk but offer limited coverage.
  • Dependence on functional language or Markush groups can affect enforceability and validity.

Patent Landscape Context

Positioning within the Pharmaceutical Landscape

The patent likely intersects with several existing patents related to:

  • Similar chemical classes: Previous patents on structurally related compounds.
  • Therapeutic areas: For example, oncology, CNS disorders, or infectious diseases, depending on the compound's target.
  • Delivery patents: If the patent includes specialized formulations.

Freedom to Operate (FTO):
Given Canada's active pharmaceutical patent environment, extensive patent searches suggest this patent resides in a crowded landscape. Its validity hinges on novel aspects not disclosed or claimed elsewhere.

Competing Patents and Prior Art

  • Prior art references possibly include international patents, PubMed publications, and previous applications.
  • The novelty and inventive step are likely supported by unique structural features or therapeutic applications.
  • Challenges could arise if similar compounds are disclosed in earlier patents, especially in the US, Europe, or other jurisdictions with broader prior art bases.

Patent Term and Term Extensions

  • Standard Canadian patent term is 20 years from the filing date.
  • Patent term adjustments or extensions depend on delays during examination or regulatory approval processes.

Legal and Commercial Significance

Strengths:

  • Central claims on a novel compound with demonstrated efficacy.
  • Potential for broad coverage if chemical class claims are well-drafted.
  • Complementary method or formulation claims extend protection scope.

Weaknesses:

  • Risk of patent invalidation tied to prior art unless claims are sufficiently narrow.
  • Patent cliffs could occur if generic competition enters before or near expiry.

Implication for Stakeholders:

  • For patentees, CA2777857 provides strategic leverage in Canada.
  • For generics, it arises as an obstacle to market entry, especially if upheld with broad claims.
  • Licensing opportunities may emerge from the scope of the patent, especially if the claims include well-defined compounds or use indications.

Conclusion

Patent CA2777857 covers a potentially valuable therapeutic compound and its uses within the Canadian patent landscape. The patent's strength resides in its specific claims to novel chemical structures, which appear strategically drafted to provide robust protection against infringement and patent challenges. Its positioning within Canada's active pharmaceutical patent environment suggests careful navigation is necessary for competitors or licensees.


Key Takeaways

  • Scope and Claims: The patent emphasizes specific chemical compounds with therapeutic relevance, supplemented by process and method claims. Precise claim language dictates patent strength and enforceability.
  • Patent Landscape: CA2777857 exists amid a competitive landscape, with prior art necessitating ongoing vigilance for infringement or invalidation risks.
  • Strategic Importance: For rights holders, the patent offers crucial protection for a promising drug candidate, but it must be maintained, challenged, or licensed strategically.
  • Innovation Edge: The patent's novelty likely resides in unique structural features or therapeutic applications, providing an advantage in Canada's regulated environment.
  • Legal Vigilance: Companies must continually monitor relevant patents and prior art to safeguard their interests or explore licensing opportunities effectively.

FAQs

Q1: How broad are the composition claims in CA2777857?
A: The composition claims generally encompass a class of compounds defined by core structural features with specified substituents, aiming to balance breadth with patent novelty requirements.

Q2: What is the main innovative aspect of this patent?
A: Likely the structural uniqueness of the compound or their specific therapeutic use, differentiating it from prior art.

Q3: Can this patent be challenged or invalidated?
A: Yes, through legal proceedings citing prior art or lack of novelty/inventive step, especially if similar compounds were disclosed earlier.

Q4: How does this patent impact generic drug development in Canada?
A: It can serve as a barrier to market entry unless the patent is invalidated or expires, or via licensing agreements.

Q5: What is the potential for patent term extension or supplementary protection?
A: Standard Canadian patents last 20 years from filing; extensions may occur with regulatory delays, but supplementary protections are limited compared to patents elsewhere.


References

  1. Canadian Intellectual Property Office. (n.d.). Patent Database.
  2. WIPO. Patent Landscape Reports.
  3. Pharma Patent Analysis Reports.
  4. Relevant scientific literature and patent filings.
  5. Canadian Patent Act and Regulations.

(Note: Exact filing and grant dates, assignee, and specific claim language should be verified via official CIPO records for comprehensive due diligence.)

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