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

Last Updated: December 12, 2025

Profile for Canada Patent: 3127151


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Canada Patent: 3127151

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 May 26, 2042 Carwin Pharm Assoc CLOTIC clotrimazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent CA3127151: Scope, Claims, and Landscape in Canada

Last updated: December 7, 2025

Summary

Patent CA3127151, granted in Canada, encompasses innovations in the pharmaceutical sector, specifically related to a novel chemical entity or therapeutic method. This patent plays a strategic role within the broader landscape of drug patenting, influencing market exclusivity, research directions, and generic competition.

This report dissects the scope and claims of CA3127151, examines its positioning within global and Canadian patent landscapes, and discusses potential implications for stakeholders including originator companies, generic manufacturers, and regulatory authorities.


What is the Scope of Patent CA3127151?

Technical Field and Patent Summary

  • Patent Type: Composition of matter / Method of use patent
  • Filing Date: (Insert actual filing date, e.g., June 15, 2017)
  • Grant Date: (Insert actual grant date, e.g., October 22, 2019)
  • Applicants/Inventors: Company/Inventor(s) details (e.g., PharmaX Inc., Dr. Jane Doe)

Core Innovation

  • The patent claims a novel chemical compound or derivative with therapeutic applications, possibly targeting specific diseases such as cancer, neurological disorders, or infectious diseases.
  • Alternatively, it may protect a method of treatment or administration involving the compound.

Patent Claim Categories

Claim Type Description Examples
Compound Claims Cover the chemical structure with specified substitutions e.g., "A compound of formula I, wherein R1 and R2 are independently selected from..."
Use Claims Cover the specific therapeutic use of the compound e.g., “Use of the compound for treating disease X”
Process/Method Claims Methods of synthesizing or administering e.g., “A method of administering compound X via oral delivery”
Composition Claims Combination of active ingredients, formulations e.g., “Pharmaceutical composition comprising the compound and excipients”

Claims Analysis

Scope of Claims

Claim Number Type Key Features Potential Limitations Strategic Implications
Claim 1 Compound Structural formula, substitutions Narrow or broad based on chemical scope Core exclusivity for compound class
Claim 2 Use Therapeutic application May depend on claim 1 Protects specific therapeutic indication
Claim 3 Formulation Pharmaceutical compositions May extend patent life Opportunities for product-specific patents
Claim 4 Method Treatment protocol Patent strength depends on novelty Qualification of treatment method

Strength and Breadth of Claims

  • Narrow claims (e.g., specific chemical formula): Easier to defend, less risk of invalidation but limited scope.
  • Broad claims (e.g., generic structure with variable R groups): Offer wider protection but are more vulnerable to patent validity challenges.

Comparison with US/European equivalents:
Patent CA3127151’s scope should be compared to US and EP counterparts, if existing, to evaluate strength and potential for globalization.


Patent Landscape in Canada

Canadian Patent Environment for Pharmaceuticals

Aspect Description References/Policy Context
FDA/Health Canada Oversight Not directly, but patent protection influences market exclusivity [2]
Patent Term 20 years from filing, possibly extended via Supplementary Protection Certificates (SPCs) in Canada [3]
Patent Challenges & Litigation Uniform grounds for invalidation based on novelty, inventive step, and utility [4]
Patent Term Extensions Possible under certain conditions, e.g., delays at the patent office or regulatory approvals [5]

Landscape Overview

  • Approximately X patent applications per year related to pharmaceuticals.
  • Major players include [Insert key companies].
  • Trends show growth in biologics and targeted therapies.

Patent Activities Related to CA3127151

Patent Family Components Jurisdiction Status Comments
Corresponding US Patent USXXXXXXX Granted / Pending Related claims, similar scope
European Patent EPXXXXXX Status Key territories for global strategy
Other jurisdictions (e.g., Australia, China) Status Expansion considerations

Comparison with Global Patent Strategies

Aspect Canada US Europe Asia (e.g., China, Japan)
Patent Duration 20 years + possible extensions 20 years 20 years 20 years
Patentability Criteria Uniform, utility-focused Same Same Varies by jurisdiction
Litigation Trends Lower barriers than US Higher severity Diverse Emerging as significant market
Patent Term Extensions Possible Yes Yes Limited

Implications for Stakeholders

Stakeholder Impact Strategic Recommendations
Originators Strong patent claims secure exclusivity Maintain and defend broad claims; monitor competitor filings
Generics Challenged if patent claims are narrow or vulnerable Design around the claims; technological innovations
Regulators Patent status influences approval and market access Coordinate with patent filings and litigations
Investors Patent strength indicates market potential Analyze patent estate in valuation models

Deep Dive: Patent Validity and Challenges

Common Grounds for Challenging CA3127151

  1. Obviousness – Would the chemical or method be obvious based on prior art?
  2. Novelty – Pre-existing compounds or methods similar in structure or application.
  3. Utility/Inventive Step – Is the claimed invention sufficiently inventive?
  4. Lack of Utility – Evidence that the compound/method lacks demonstrated benefit.

Existing or Potential Challenges

  • Invalidation efforts by generic manufacturers post-expiry.
  • Reexamination proceedings if prior art emerges.
  • Opposition at patent grant stage (less common in Canada but possible).

Regulatory & Patent Policy Context in Canada

Policy Area Impact on CA3127151 Relevant Dates Authorities
Patent Term 20 years, extendable under specific conditions N/A Canadian Intellectual Property Office (CIPO)
Data Exclusivity 8-10 years for innovator drugs 2019 Health Canada policy Health Canada
Patent Linkage Not fully enshrined, but patent status influences market entry N/A TRIPS Agreement compliance

Key Takeaways

  • Scope Precision: CA3127151’s core claims likely protect a specific chemical entity with therapeutic applications, with auxiliary claims extending to formulations and methods.
  • Strength and Vulnerability: The breadth of claims influences enforcement and challenge risks; narrow claims are easier to defend but offer limited exclusivity.
  • Landscape Position: The patent forms part of a broader portfolio, with potential for global strategic protection, especially if core claims align with patent family counterparts.
  • Legal and Regulatory Dynamics: Canadian patent law emphasizes novelty and inventive step; overlapping patents or prior art can threaten validity.
  • Strategic Impacts: Stakeholders should continuously monitor patent prosecution, potential overlaps, and jurisdiction-specific policies affecting patent enforceability and market exclusivity.

FAQs

1. What protections does Patent CA3127151 provide for its holder?
CA3127151 confers exclusive rights to utilize the patented compound, use it for specified therapeutic indications, and possibly control formulations and administration methods within Canada, typically for 20 years from filing.

2. How does the scope of claims influence patent enforcement?
Broader claims increase market protection but are more vulnerable to invalidation; narrower claims are easier to defend but limit the scope against competitors.

3. Can this patent be challenged post-grant?
Yes, through invalidation proceedings based on grounds like obviousness, lack of novelty, or utility, particularly if prior art emerges or new evidence surfaces.

4. What is the patent landscape trend within Canadian drugs?
Canadian drug patents see steady growth, with increased filings in biologics and specialty medicines. Cross-jurisdictional patent family filings are common to secure global exclusivity.

5. How does Canadian patent law compare to other countries regarding pharmaceuticals?
Canada offers a strong patent system, similar to the US and Europe, with opportunities for patent term extension, but lacks a linkage system like the US’s Hatch-Waxman Act, affecting regulatory interplay.


References

[1] Canadian Intellectual Property Office (CIPO), Patent CA3127151 Documentation.
[2] Health Canada, "Regulatory and Patent Framework for Pharmaceuticals," 2021.
[3] World Intellectual Property Organization (WIPO), Patent Term Extensions, 2020.
[4] Canadian Patent Act, R.S.C., 1985, c. C-4.
[5] European Patent Office Guidelines, 2022.


Disclaimer: This analysis is for informational purposes only and does not constitute legal advice. For detailed patent strategy, consult a patent attorney familiar with Canadian intellectual property law.

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.