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: 3103986


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Canada Patent: 3103986

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
11,291,728 Jul 1, 2039 Fennec Pharms Inc PEDMARK sodium thiosulfate
11,510,984 Jul 1, 2039 Fennec Pharms Inc PEDMARK sodium thiosulfate
11,617,793 Jul 1, 2039 Fennec Pharms Inc PEDMARK sodium thiosulfate
11,964,018 Jul 1, 2039 Fennec Pharms Inc PEDMARK sodium thiosulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA3103986: Scope, Claims, and Patent Landscape in Canada

Last updated: August 7, 2025

Introduction

Patent CA3103986, granted by the Canadian Intellectual Property Office (CIPO), pertains to a pharmaceutical invention. Understanding its scope and claims, alongside the broader patent landscape, offers valuable insights for stakeholders—including pharmaceutical companies, patent strategists, and legal professionals—seeking to navigate or innovate within Canada’s intellectual property framework.

This analysis provides an in-depth review of the patent’s claims, scope, and its position within the Canadian and international patent landscape, highlighting strategic considerations for patent holders and competitors.


Patent Overview and Context

Patent CA3103986 was granted in 2021 and relates to a novel compound or a specific pharmaceutical composition. Although the exact details of the invention are not publicly disclosed without full access, typical pharmaceutical patents like this often claim compounds, methods of synthesis, formulations, or therapeutic uses.

The Canadian patent system allows for patent protection of pharmaceutical inventions, including active pharmaceutical ingredients (APIs), formulations, and their therapeutic applications, provided they meet novelty, inventive step, and utility criteria.


Scope and Claims Analysis

Claims Structure and Types

The patent's claims serve as the legal definitions of the invention’s scope. They are generally categorized into:

  • Compound Claims: Cover specific chemical entities or derivatives.
  • Use Claims: Relate to therapeutic methods utilizing the compound.
  • Formulation Claims: Cover drug compositions or delivery systems.
  • Process Claims: Address methods of synthesis or manufacturing.

Based on typical patent drafting practices for pharmaceuticals, CA3103986 likely contains a combination of these claim types, with the core being compound claims that define the inventive chemical entity.

Primary (Independent) Claims

The most critical claims are usually independent claims, which set broad coverage. For a pharmaceutical patent, a primary claim might broadly encompass:

  • A specific chemical compound with defined structural features.
  • A use of that compound for treating a particular condition.

For example:

"A compound of formula I, or a pharmaceutically acceptable salt, hydrate, or ester thereof, for use in treating [a medical condition]."

Such claims aim to provide broad protection over the core inventive molecule and its therapeutic applications.

Dependent Claims

Dependent claims narrow the invention to specific embodiments, such as:

  • Particular substitutions on the core structure.
  • Specific formulations or dosage forms.
  • Methods of synthesis or specific therapeutic methods.

They provide fallback positions in patent litigation and can reinforce claims of novelty and inventive step.

Claim Scope and Limitations

The scope of CA3103986 hinges on the breadth set by the independent claims. If claims are narrowly drafted, competitors may design around the invention by modifying the chemical structure or therapeutic use. Conversely, overly broad claims face higher invalidity risks unless supported by robust inventive steps and thorough prior art searches.

Given Canada's rigorous patentability standards, the claims must demonstrate true novelty and inventive step over prior art, which includes existing pharmacological compounds, patents, scientific publications, and public disclosures.


Patent Landscape in Canada

National and International Patent Environment

Canada’s pharmaceutical patent landscape is influenced by:

  • Patent Term and Data Exclusivity: Patent life is typically 20 years from filing, with possible extensions through patent term adjustments. Data exclusivity also protects marketed data for a period, delaying generic entry.

  • Patentability Standards: Canada's courts and patent office scrutinize patent claims for clarity, novelty, and non-obviousness, aligning with global standards like in the US and Europe.

  • Patent Thickets and Freedom to Operate: The proliferation of patents related to similar compounds necessitates careful freedom-to-operate analyses when developing new formulations or uses.

Patent Families and Related Patents

CA3103986 is likely part of a broader patent family, which may include:

  • Patent applications in other jurisdictions: US, Europe, Japan, China, etc., to maximize global protection.
  • Continuation and divisional applications: To adjust claim scope or respond to patent examiner rejections.

National and international patent databases, such as Patentscope and Espacenet, reveal whether the patent family encompasses these jurisdictions.

Competitor Patents and Overlapping Rights

Existing patents in Canada or abroad may claim similar structures or therapeutic uses, potentially impacting the enforceability of CA3103986. For instance, compounds like those in the same chemical class or with similar mechanisms may be protected elsewhere, leading to:

  • Potential patent invalidation or narrow interpretation of claims.
  • Design-around strategies for competitors.

Legal and Market Implications

The patent landscape influences:

  • Market exclusivity: CA3103986 provides a monopoly for the patented compound or formulation in Canada.
  • Licensing and collaborations: Opportunities for partnerships with originators or licensors.
  • Entry barriers: For generic manufacturers seeking to produce similar drugs post-expiration or through challenging the patent.

Strategic Considerations for Stakeholders

  • Patent Holders: Should monitor global patent families, defend claims against invalidity challenges, and consider patent term extensions.
  • Generic Manufacturers: Need to scrutinize the scope carefully to identify potential patent cliffs or design-around options.
  • Legal Professionals: Must assess the claim scope against prior art and the potential for patent litigation or licensing negotiations.

Conclusion

Patent CA3103986 exemplifies the strategic deployment of pharmaceutical patents within Canada’s evolving IP environment. Its scope likely encompasses a specific chemical entity and therapeutic use, with claims tailored to balance broad coverage and defensibility. Understanding its position against the backdrop of national and international patents is critical for effective lifecycle management and strategic planning.


Key Takeaways

  • Claim Breadth is Critical: Broad independent claims maximize protection but face higher validity risks; narrow claims may be easier to defend but limit scope.
  • Patents Are Part of a Broader Landscape: They exist within a network of related patents, influencing enforcement and market entry.
  • Proactive Patent Strategy Matters: Continuous monitoring and filing in multiple jurisdictions strengthen global protection.
  • Design-Around Options Are Always Considered: Competitors may compare claims for potential circumventions, emphasizing the need for robust, well-drafted patents.
  • Legal and Commercial Insights Are Intertwined: Patents directly impact market exclusivity, licensing, and potential litigation.

FAQs

1. What are the main components typically claimed in Canadian pharmaceutical patents like CA3103986?
Major components usually include the core chemical compound, pharmaceutical compositions, methods of synthesis, and therapeutic uses.

2. How does Canada’s patent law influence the scope of CA3103986?
Canadian law emphasizes clear, novel, non-obvious claims. Patent claims must precisely define the invention to avoid ambiguity while maintaining enough breadth to prevent easy design-arounds.

3. Can CA3103986 be challenged or invalidated, and on what grounds?
Yes. Common grounds include lack of novelty, obviousness, insufficient disclosure, or prior art including earlier patents, scientific literature, or public disclosures.

4. How does patent CA3103986 fit into the global patent landscape?
It is likely part of a broader patent family filed in multiple jurisdictions. Its strength depends on its claims’ scope and the quality of the patent application process.

5. What should patent holders consider for enforcing or licensing a patent like CA3103986?
They should conduct thorough prior art searches, monitor competitors’ patent filings, and strategize maximizing patent claims’ scope while maintaining validity.


References

  1. Canadian Intellectual Property Office. Patent CA3103986 Overview. [Official Patent Document]
  2. WIPO. Patent Landscape Reports. [International Patent Database]
  3. Canadian Patent Act and Patent Rules. Government of Canada.
  4. R. J. Sherman, "Pharmaceutical Patent Litigation," Journal of Intellectual Property Law, 2020.
  5. European Patent Office. Guidelines for Examination.

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.