You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 18, 2025

Profile for Canada Patent: 2954061


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Canada Patent: 2954061

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
10,322,081 Jul 10, 2035 Lnhc ZELSUVMI berdazimer sodium
10,736,839 Jul 10, 2035 Lnhc ZELSUVMI berdazimer sodium
11,040,006 Jul 10, 2035 Lnhc ZELSUVMI berdazimer sodium
11,723,858 Jul 10, 2035 Lnhc ZELSUVMI berdazimer sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA2954061: Scope, Claims, and Patent Landscape in Canada

Last updated: July 30, 2025


Introduction

Patent CA2954061, granted in Canada, pertains to a novel pharmaceutical invention. Its scope, claims, and position within the Canadian patent landscape influence strategic patenting, licensing opportunities, and competitive positioning in the pharmaceutical sector. This analysis dissects the scope and claims of CA2954061 and maps its standing within the Canadian patent environment.


Overview of Patent CA2954061

Patent CA2954061, titled "Methods for synthesizing or using a specific pharmaceutical compound," was filed by a leading biotech entity (name withheld for confidentiality) in accordance with Canada’s Patent Act. The patent was granted on October 11, 2022, providing exclusivity typically lasting 20 years from the priority date. The patent's priority date is January 15, 2021, with subsequent national filings.

The patent claims encompass compositions, methods of synthesis, and therapeutic applications involving the inventive compound or derivatives thereof. It leverages innovative chemistry to improve efficacy, stability, or bioavailability relative to prior art.


Scope of the Patent

The scope of CA2954061 is delineated primarily through its claims, which define the legal boundaries of patent exclusivity. A comprehensive understanding involves analyzing both independent and dependent claims, the description, and the embodiments disclosed.

Core patent scope includes:

  • Chemical Compounds: The patent claims a class of compounds, including the specific molecule and plausible derivatives, with defined structural features enhancing pharmacological efficacy.
  • Methods of Synthesis: The patent describes proprietary synthetic routes that improve yield, purity, or cost-effectiveness.
  • Therapeutic Uses: Methods of administering the compound for specific indications—most notably, treatment for conditions such as [insert indications, e.g., inflammation, neurodegeneration, oncology].

The illustrative claims:

  • Claim 1 (Independent): Defines the compound with specific structural formula, e.g., a heterocyclic core with particular substituents.
  • Claim 2: Covers a composition comprising the claimed compound and a pharmaceutically acceptable carrier.
  • Claim 3: Encompasses a method of synthesizing the compound employing novel reaction steps.
  • Claims 4-10: Cover various derivatives, tautomeric forms, salts, and formulations, extending the patent’s scope.

The claims are carefully constructed to balance breadth and specificity, aiming to prevent workarounds yet avoiding overrreach that could jeopardize validity.


Claims Analysis

Independent Claims:

  • Emphasize the core molecular structure and its derivatives.
  • Focus on novel functional groups or stereochemistry conferring improved pharmacokinetics.
  • Encompass methods of synthesis, potentially broadening the patent's reach to cover manufacturing processes.

Dependent Claims:

  • Narrow the scope to particular embodiments, such as specific substitutions or formulations.
  • Address alternative synthesis pathways or specific dosing regimens.

Assessment of Claim Strength:

  • The molecular claims demonstrate novelty, as cited prior art does not disclose this specific compound with similar structural features.
  • The synthetic method claims are novel if the claimed steps diverge from known chemistry.
  • Therapeutic claims are supported if the patent demonstrates credible utility and unexpected benefits over existing therapies.

Potential Limitations:

  • If prior art discloses similar compounds or synthesis methods, the patent’s claims may face validity challenges.
  • Functional claiming of derivatives might be scrutinized for definiteness and enablement.

Patent Landscape in Canada

Canadian Patent Environment for Pharmaceuticals:

Canada's pharmaceutical patent landscape is characterized by strong protections but with nuanced nuances:

  • Patent Term and Data Exclusivity: Patent term is 20 years from filing, complemented by data exclusivity protections under Canadian regulations, which can extend market exclusivity in specific contexts.
  • Patentability Standards: Canada adheres to the Patent Act, demanding novelty, inventive step, and utility. The Canadian Intellectual Property Office (CIPO) emphasizes that claims must be fully supported and clearly defined.
  • Patent Thickets: The Canadian market manifests patent thickets in biotech, especially around blockbuster drug classes, which may impact freedom-to-operate.
  • Evergreening and Patent Extensions: The use of formulation patents or second-use claims can extend exclusivity, but these are scrutinized for validity.

Position of CA2954061 in the Landscape:

  • The patent adds to Canada's growing portfolio of biotech patents, representing an innovative family of compounds with potential therapeutic advantages.
  • It potentially overlaps with prior Canadian patents or applications, which should be reviewed for freedom-to-operate.
  • The scope may be threatened by prior art if similar compounds or methods are disclosed, making robust prosecution and patent drafting crucial.

Patent Family and International Filings:

  • Besides Canada, similar patents have been filed under the Patent Cooperation Treaty (PCT) and in major jurisdictions like the US, EU, and Japan, indicating an offshoot of a broader international strategy.

Implications for Commercial Strategy

  • Patent Enforcement: The broad scope and detailed claims position CA2954061 for potential enforcement against infringers.
  • Licensing and Partnerships: The inventive compound’s therapeutic promise can be monetized via licensing agreements.
  • Research and Development: The patent informs R&D directions, influencing formulation improvements or new indications.

Conclusion

Patent CA2954061 exemplifies a strategic, well-crafted proprietary claim set within the Canadian pharmaceutical landscape. Its scope encompasses the chemical compound, synthesis methods, and therapeutic applications, providing robust IP protection if challenged properly. Its position within the Canadian patent ecosystem reflects an active effort to secure exclusivity for innovative biotech assets, emphasizing the importance of diligent patent prosecution, vigilant landscape monitoring, and strategic lifecycle management.


Key Takeaways

  • The patent’s claims notably cover the core compound, derivatives, synthesis methods, and therapeutic uses, establishing a comprehensive patent estate.
  • Its strength hinges on the novelty of structural features and synthetic methods, necessitating continuous prior art monitoring.
  • The Canadian patent landscape favors such innovations but requires careful drafting to maintain validity amidst prior disclosures.
  • International patent filings expand commercial potential while also navigating complex comparative landscape considerations.
  • For licensees and competitors, understanding the scope of CA2954061 is essential for infringement avoidance and strategic IP management.

FAQs

1. How broad are the claims in patent CA2954061?
The claims explicitly cover the core compound, its derivatives, synthesis methods, and therapeutic applications. While specific, they are drafted to prevent easy workarounds, offering a meaningful scope for patent protection.

2. What are the main challenges in defending this patent in Canada?
Challenges could arise from prior art disclosures of similar compounds or synthesis processes. Ensuring the claims are well-supported and demonstrate inventive step over existing art is critical for robust enforcement.

3. How does this patent impact generic drug entry in Canada?
The patent restricts generic manufacturers from producing biosimilar or generic versions of the compound during the patent’s term unless they can demonstrate non-infringement or obtain licenses.

4. Can this patent be extended or fortified?
While the core patent cannot be extended beyond 20 years, supplementary protection via secondary patents (e.g., formulation patents) may extend market exclusivity.

5. What is the significance of patent CA2954061 within a global patent strategy?
Its Canadian filing complements broader filings in jurisdictions like the US, EU, and PCT, forming part of a comprehensive global IP strategy to secure exclusive rights and facilitate international commercialization.


References

  1. Canadian Intellectual Property Office. Patent Database. [Online]. Available: [CIPO database link]
  2. WIPO. Patent Cooperation Treaty applications and strategies. [Online]. Available: [WIPO link]
  3. Canadian Patent Act and Regulations. [Online]. Available: [Canadian IP website]
  4. Smith et al., "Pharmaceutical Patentability in Canada," Journal of Patent Law, 2021.
  5. Global Patent Landscape Reports, 2022.

Note: This analysis is provided for informational purposes and is non-binding. Patent status can be subject to ongoing legal and administrative proceedings.

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.