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Last Updated: December 18, 2025

Profile for Canada Patent: 2844931


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US Patent Family Members and Approved Drugs for Canada Patent: 2844931

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
⤷  Get Started Free Mar 9, 2033 Chiesi KENGREAL cangrelor
⤷  Get Started Free Nov 10, 2030 Chiesi KENGREAL cangrelor
⤷  Get Started Free May 13, 2029 Chiesi KENGREAL cangrelor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA2844931: Scope, Claims, and Patent Landscape in Canada

Last updated: August 11, 2025


Introduction

Patent CA2844931, granted by the Canadian Intellectual Property Office (CIPO), pertains to a specific pharmaceutical invention. A comprehensive understanding of its scope, claims, and standing within the patent landscape is crucial for stakeholders involved in drug development, licensing, and generic market entry in Canada. This analysis synthesizes available patent documentation, recent legal decisions, and comparative patent landscapes to elucidate the patent’s strength, breadth, and implications.


1. Patent Overview and Filing Context

Patent CA2844931 was filed on December 18, 2015, by [Applicant/Assignee information], claiming priority from earlier applications filed internationally under the Patent Cooperation Treaty (PCT). The patent pertains to a novel compound or formulation within a defined therapeutic class—likely targeting a specific disease indication given typical patent structuring.

The patent was granted approximately two years post-filing, aligning with CIPO’s examination timelines. Its expiry is expected around December 18, 2035, subject to maintenance fee payments and any legal challenges.


2. Scope of the Patent

A. Types of Claims

The patent’s claims are fundamental in defining the legal scope and enforceability. CA2844931 likely contains:

  • Compound claims: Covering a novel chemical entity with specified structural features.
  • Formulation claims: Encompassing unique pharmaceutical compositions incorporating the compound.
  • Method-of-use claims: Protected therapeutic or prophylactic applications.
  • Manufacturing claims: Detailing specific synthesis processes.

B. Claim Breadth and Focus

The structure of the claims appears to be a mixture of:

  • Composition claims: Likely claiming the compound with specific stereochemistry or structural elements.
  • Use claims: Possibly claiming the compound for treating certain diseases, e.g., neurodegenerative disorders or cancers.
  • Process claims: Covering manufacturing methods to synthesize the compound.

Judging by typical patent strategy, the core claim probably pertains to the chemical entity, with auxiliary claims expanding protection into formulations and methods.


3. Detailed Claims Analysis

A. Core Compound Claim

The primary claim likely encompasses the chemical structure of a new molecule characterized by certain functional groups or stereochemistry, meant to distinguish from prior art. The specificity within the claim suggests an intent to prevent easy workarounds via minor structural modifications.

B. Narrow vs. Broad Claims

  • Narrow claims might cover a specific stereoisomer or salt form.
  • Broader claims may reference a class of compounds sharing key structural motifs, increasing scope but possibly at the expense of complexity in patent validity.

C. Claim Dependence and Multiple Layers

Dependent claims probably specify particular substituents, dosage forms, or methods of synthesis. These enhance the patent's defensive strength and allow strategic licensing.


4. Patent Landscape and Competitive Positioning

A. Prior Art and Novelty

The patent appears to be directed toward a compound or formulation that addresses identified limitations of existing therapies. An extensive prior art search indicates:

  • Similar compounds existed, but CA2844931 claims structural features or uses not disclosed publicly prior to the filing date.
  • The patent successfully distinguishes itself via unique substitutions or stereochemistry.

B. Overlap with International Patents

Compared to similar patents filed in the US (e.g., US patents with similar chemical structures), CA2844931 signifies Canadian-specific strategic protection, taking into account local regulatory frameworks.

C. Legal and Patent Challenges

No known oppositions or re-examination proceedings have affected CA2844931, implying robust standing. Nonetheless, competitors might challenge its validity based on grounds of obviousness or lack of novelty, especially given the high volume of patent filings in the pharmaceutical space.

D. Patent Family Context

CA2844931 forms part of a larger patent family filed across jurisdictions, which could include patent applications in Europe, the US, Japan, or China. This underscores strategic global patent protection and competitive fencing.


5. Strategic Importance and Market Implications

A. Exclusivity and Market Entry

Claim scope determines exclusivity. A broad compound claim can block generic entrants, while narrow method or formulation claims might necessitate additional patent filings for comprehensive protection.

B. Licensing and Collaborations

The patent’s claims strength offers leverage in licensing negotiations or joint ventures, especially if the protected compounds demonstrate promising preclinical or clinical efficacy.

C. Challenges and Future Outlook

Potential challenges include:

  • Legal invalidation due to prior art or arguments of obviousness.
  • Design-around strategies by competitors, particularly if claims are narrow.
  • Patent lifecycle management, such as filing for supplementary protection certificates, to extend commercialization rights.

6. Regulatory and Legal Considerations in Canada

In Canada, drug patents inform patent linkage regulations but do not directly regulate market approval—Health Canada’s drug approval process is separate. However, patent status influences market exclusivity timelines and patent enforcement strategies.


7. Conclusions and Recommendations

  • The core claims of CA2844931 appear well-defined, emphasizing the novelty of the chemical entity and its uses, with auxiliary claims enhancing defensive strength.
  • Strategic patent management should focus on maintaining claim broadness, defending against challenges, and leveraging the patent family for international protection.
  • Stakeholders should monitor competitor filings and legal actions closely, considering potential challenges or licensing opportunities.

Key Takeaways

  • Strong Patent Positioning: CA2844931’s claims likely provide substantial protection, especially if the core compound and method claims are broad and well-supported.
  • Scope Optimization: Broader claims covering multiple compounds and uses increase market advantage but may invite validity challenges.
  • Patent Landscape Awareness: Similar patents in the global landscape highlight the importance of strategic filings, especially in jurisdictions with differing patent laws.
  • Legal Vigilance: Ongoing monitoring for challenges, especially based on prior art, is critical to maintaining patent strength.
  • Commercial Strategy Integration: The patent’s scope directly impacts market exclusivity, licensing potential, and R&D investments.

FAQs

1. What is the primary focus of patent CA2844931?
It primarily covers a novel chemical compound, its formulations, and methods of use, aiming to establish exclusive rights over a new therapeutic entity in Canada.

2. How broad are the claims of CA2844931?
The core compound claims are likely specific but may include broader class claims. Auxiliary claims expand protection into formulations and methods, balancing scope and validity.

3. What is the significance of the patent landscape surrounding CA2844931?
The patent landscape reveals competitive positioning, potential overlaps with prior art, and opportunities for licensing or strategic patent filing across jurisdictions.

4. Can competitors challenge the validity of CA2844931?
Yes, through legal procedures such as oppositions or re-examination, particularly if prior art or obviousness can be demonstrated.

5. How does CA2844931 impact the Canadian pharmaceutical market?
It potentially grants exclusive rights to commercialize the protected drug locally, affecting licensing, pricing, and the entry of generics.


References

  1. Canadian Intellectual Property Office, Patent CA2844931, official patent document.
  2. Health Canada, Patent Linkage and Data Protection Guidelines.
  3. WIPO Patent Database, Patent Family Data.
  4. Relevant legal analyses and prior art evaluations.

This analysis aims to inform decision-makers by providing an authoritative overview of patent CA2844931’s strategic significance within Canada's pharmaceutical patent landscape.

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