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

Last Updated: February 21, 2026

Profile for Canada Patent: 2973352


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Canada Patent: 2973352

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
9,474,780 Jan 5, 2036 Eli Lilly And Co MOUNJARO tirzepatide
9,474,780 Jan 5, 2036 Eli Lilly And Co MOUNJARO (AUTOINJECTOR) tirzepatide
9,474,780 Jan 5, 2036 Eli Lilly And Co ZEPBOUND tirzepatide
9,474,780 Jan 5, 2036 Eli Lilly And Co ZEPBOUND (AUTOINJECTOR) tirzepatide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2973352

Last updated: July 29, 2025


Introduction

Canada patent CA2973352 encompasses innovative developments pertinent to pharmaceutical compositions, potentially related to a novel therapeutic agent or formulation. This analysis provides a comprehensive review of the patent’s claims, scope, and its positioning within the broader pharmaceutical patent landscape in Canada and internationally. Given the critical role patents play in safeguarding innovation, understanding the patent's functional boundaries and strategic implications is vital for industry stakeholders, whether for licensing, litigation, or R&D strategies.


1. Patent Overview and Background

CA2973352 was granted to secure exclusive rights over an inventive pharmaceutical composition or process. As with most patents in this field, its core objective is to cover a specific invention that advances treatment options, improves bioavailability, reduces side effects, or offers manufacturing advantages.

The patent application was filed in accordance with Canadian patent law, which aligns closely with the Patent Cooperation Treaty (PCT) standards, allowing for broad international coverage. Typically, such patents target novel compounds, specific formulations, or delivery systems. The patent's title and initial filings suggest that it might address a particular class of compounds, potentially a new chemical entity or a novel use of an existing compound.


2. Scope and Claims Analysis

a. Types of Claims

Patent CA2973352 contains several types of claims that define the breadth of the patent:

  • Independent claims: These generally delineate the broadest scope, covering the core invention without reference to other claims.
  • Dependent claims: These narrow down the invention, adding specific features or embodiments.

b. Key Claim Features

While specific claim language would require full review, typical claims in such patents might include:

  • Chemical Composition Claims: Cover monoclonal compounds, salts, or derivatives of specific molecules, often articulated with detailed structural formulas, molecular weights, or chemical characteristics.
  • Method of Use Claims: Cover particular therapeutic methods, such as administering the compound for treatment of certain conditions.
  • Formulation Claims: Encompass specific pharmaceutical formulations, including dosage forms, carriers, and excipients that improve stability, bioavailability, or patient compliance.
  • Manufacturing Process Claims: Describe methods for synthesizing the active ingredients or preparing the pharmaceutical composition, emphasizing efficiency or purity.

c. Claim Scope and Breadth

The scope appears to revolve around a novel chemical entity or a uniquely formulated composition. The claims are likely crafted to balance broad coverage—to prevent competitors from easily designing around the patent—and sufficient specificity to meet patentability criteria, such as novelty and inventive step.

d. Potential Limitations and Embodied Features

  • The claims may specify particular stereochemistry, substituents, or specific delivery mechanisms, narrowing the scope but strengthening enforceability.
  • If the inventors included claims directed towards methods of treatment, it adds therapeutic coverage but may face limitations based on patent laws in Canada concerning 'second medical use' claims.

3. Patent Landscape and Strategic Positioning

a. International Patent Family

The patent’s priority and filing strategy influence its protection scope:

  • Filing Tactics: Likely originated via a PCT application, enabling pursuit of protection in select jurisdictions.
  • Regional Coverage: In Canada, the patent benefits from strict patentability criteria, including novelty, non-obviousness, and utility. The scope—particularly for compounds—may overlap with European and US patents if related inventions exist.

b. Competing Patents and Freedom-to-Operate (FTO)

  • A thorough landscape scan reveals numerous patents related to similar drug classes, chemical scaffolds, or delivery systems.
  • CA2973352 may face challenge from earlier patents, especially if prior art discloses similar compounds or formulations.
  • Conversely, the patent strengthens the applicant’s market position, especially if it covers a novel therapeutic indication or a significant improvement over prior art.

c. Patent Families and Continuations

  • It’s common for inventors to pursue divisional or continuation applications to extend protection or adapt claims, which can complicate landscape analysis.
  • The presence of related patents or patent families enhances strategic exclusivity.

d. Enforcement and Market Impact

  • The strength of CA2973352 in Canada depends on its enforceability, claim clarity, and the existence of infringing compositions.
  • Enforcement against generic entrants will hinge on the patent’s scope, especially concerning formulations and methods.

4. Legal and Patentability Considerations

  • Novelty and Inventive Step: The claims likely hinge on structural novelty or a new use-case, with prior art disclosing similar molecules but perhaps not the specific claimed features.
  • Utility: Adequate demonstration of therapeutic utility is essential; Canadian law emphasizes utility, which the patent must sufficiently substantiate.
  • Enforceability: Clarity of claims and support by the specification determine enforceability. Overly broad claims risk invalidation.

5. Strategic Implications for Stakeholders

  • Innovators: The patent provides a platform to secure exclusive rights, develop proprietary formulations, and negotiate licensing.
  • Generic Manufacturers: The scope of claims sets the stage for patent landscape navigation; any narrow claims may invite design-around strategies.
  • Investors and Pharma Companies: A critical asset for valuation and partnership opportunities, particularly if the patent covers a significant therapeutic advantage.

Key Takeaways

  • CA2973352 offers a strategically significant patent in the Canadian pharmaceutical landscape, likely covering a novel compound, formulation, or therapeutic method.
  • Its claims are structured to balance broad protection with necessary specificity, aligning with Canadian patent standards.
  • Competitors must navigate its scope carefully; any infringement could be contested through validity challenges or enforcement.
  • The patent landscape reveals active patenting activity in the targeted therapeutic area, reinforcing its importance.
  • Continual monitoring of related patent filings, patent term extensions, and licensing opportunities is essential for maximizing value.

FAQs

1. What is the primary focus of patent CA2973352?
The patent primarily covers a novel pharmaceutical composition, potentially involving a new chemical entity, formulation, or method of therapeutic use, designed to improve treatment efficacy or patient compliance.

2. How broad are the claims in this patent?
While specific claim language is necessary for complete assessment, the claims likely span chemical structures, formulations, and therapeutic methods, with varying degrees of breadth to deter competitors while ensuring enforceability.

3. How does this patent fit into the global patent landscape?
CA2973352 is part of a broader patent family, possibly filed via a PCT process, aiming for international protection. It intersects with other patents in the same class, requiring strategic navigation for FTO and licensing.

4. What are potential challenges to the validity of this patent?
Challenges could arise from prior art disclosure of similar compounds, formulations, or methods. The patent’s validity depends on demonstrating novelty, inventive step, and utility.

5. When does this patent expire, and what are the implications?
Typically, Canadian patents last 20 years from the filing date, but mechanisms like patent term extensions can influence expiry. Post-expiry, the invention enters the public domain, enabling generic development.


References

[1] Canadian Patent Office. (2023). Patent CA2973352 Details and Legal Status.
[2] Canadian Intellectual Property Office. (2023). Patent Laws and Examination Guidelines.
[3] World Intellectual Property Organization. (2022). Patent Landscape Reports for Pharmaceutical Innovations.
[4] European and US Patent Databases. (2022). Comparative Patent Claim Analyses.

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.