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Last Updated: December 12, 2025

Profile for Canada Patent: 2875824


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US Patent Family Members and Approved Drugs for Canada Patent: 2875824

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
10,980,795 Jun 12, 2033 Ipsen ONIVYDE irinotecan hydrochloride
11,369,597 Jun 12, 2033 Ipsen ONIVYDE irinotecan hydrochloride
12,364,691 Jun 12, 2033 Ipsen ONIVYDE irinotecan hydrochloride
9,339,497 Jun 12, 2033 Ipsen ONIVYDE irinotecan hydrochloride
9,364,473 Jun 12, 2033 Ipsen ONIVYDE irinotecan hydrochloride
9,452,162 Jun 12, 2033 Ipsen ONIVYDE irinotecan hydrochloride
9,492,442 Jun 12, 2033 Ipsen ONIVYDE irinotecan hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2875824

Last updated: August 3, 2025

Introduction

Canada patent CA2875824 pertains to innovative developments within the pharmaceutical sector, possibly related to novel drug formulations, delivery mechanisms, or therapeutic methods. To fully appreciate its strategic importance, an in-depth analysis of its scope, claims, and the broader patent landscape is essential. This review provides a comprehensive examination, useful for pharmaceutical stakeholders, patent professionals, and legal entities involved in drug development and intellectual property management in Canada.


Scope of Patent CA2875824

The scope of a patent determines the breadth of protection conferred by its claims. Patent CA2875824's scope hinges on its specific claims and descriptive content, delineating the boundaries of exclusivity.

Overview of the Patent Content

Although detailed specifics of CA2875824 are not publicly available in this context, typical pharmaceutical patents in Canada encompass:

  • Compound patents: Covering novel chemical entities or biologics.
  • Use patents: Relating to new therapeutic indications or diagnostic methods.
  • Formulation patents: Protecting specific pharmaceutical compositions or delivery systems.
  • Process patents: Covering manufacturing or synthesis methods.

Given the typical structure, CA2875824 likely emphasizes one or multiple of these categories, aiming to secure exclusive rights over a novel compound, its therapeutic use, or an innovative formulation.

Canadian Patent Law Context

Canadian patent law, governed by the Patented Medicine (Notice of Compliance) Regulations and Patent Act, emphasizes the novelty, inventive step, and utility of pharmaceutical inventions. The patent’s scope is interpreted analytically through its claims, which must be clear, concise, and supported by the description.


Claims Analysis of CA2875824

The patent's claims define its legal scope and are critical for licensing, infringement, and litigation considerations.

Type of Claims

Based on standard practice, CA2875824 may include:

  • Independent claims: Broad claims outlining the core inventive concept.
  • Dependent claims: Narrower claims that specify particular embodiments or innovations.

Hypothetical Claim Structure

  • Compound Claims: Claiming a chemical entity with specific structural features, such as a novel molecular scaffold, stereochemistry, or substituents.
  • Use Claims: Claiming the use of the compound for treating particular diseases, e.g., cancer, neurological disorders, or infectious diseases.
  • Formulation Claims: Covering unique formulations, such as controlled-release matrices or combination therapies.
  • Process Claims: Detailing synthesis methods or formulation processes.

Evaluation

The strength and scope depend on the specificity of the claims—broad claims afford extensive protection but are more vulnerable to invalidation, whereas narrow claims provide limited scope but stronger defensibility.

Claim Language and Patent Validity

Canada’s patent doctrine emphasizes that claims must meet the criteria of novelty, inventive step, and utility:

  • Novelty: No prior art must disclose the same invention.
  • Inventive Step: The invention must be non-obvious to those skilled in the art.
  • Utility: The invention must have a specific, substantial, and credible utility.

If the claims are sufficiently differentiated from existing patents and prior art, they can withstand legal challenges.


Patent Landscape for Similar Technologies in Canada

Understanding the patent environment around CA2875824 is vital, especially considering existing patents, prior art, and prospective freedom-to-operate (FTO).

Existing Patent Frailties and Opportunities

  • Overlap with prior art: Key patents concerning similar chemical scaffolds or therapeutic uses may exist, potentially creating infringement risks.
  • Patent Thickets: The pharmaceutical landscape often involves dense patent clusters, making FTO assessments critical before commercialization.
  • Litigation and Litigation Risks: Canadian courts have seen increased patent disputes around biologics and drug formulations, influencing strategic patenting.

Competitive Landscape

  • International Patent Families: Many pharmaceutical innovations are protected via patents across multiple jurisdictions, including the U.S., Europe, and China, impacting Canadian patent strength.
  • Patentability Trends: Trends show increased patent protection for biologics, personalized medicine, and combination therapies, aligning with technological progress.

Strategic Implications for Patent CA2875824

Innovation Positioning

Given the evolving pharmaceutical landscape, CA2875824's protection should aim at encompassing core innovations and subsequent refinements:

  • Broad Claims Strategy: To establish a protective moat, especially if the innovation involves a novel compound or use.
  • Dependent Claims: To provide fallback positions and safeguard incremental improvements.

Patent Term & Lifecycle

  • Patent Term: Generally 20 years from the filing date, which must be optimized with patent filing strategies to maximize market exclusivity.
  • Evergreening Strategies: Filing divisional applications or related patents can extend market control.

Freedom to Operate & Licensing Opportunities

  • FTO Analyses: Essential prior to commercialization to avoid infringing existing patents.
  • Partnerships and Licensing: Opportunities for licensing may arise if CA2875824 overlaps with or complements existing patent portfolios.

Conclusion: Patent CA2875824’s Position and Future Outlook

While specific claims details are not publicly disclosed, the general analysis suggests that CA2875824 represents a targeted effort to protect a novel drug or formulation. Its scope likely balances broad protection with claim specificity, aligning with Canadian patent law. The patent landscape indicates a competitive environment necessitating strategic claim drafting, vigilant freedom-to-operate analysis, and ongoing patent portfolio management to sustain market advantage.


Key Takeaways

  • Scope and claims: Well-drafted claims centered on a novel chemical entity, therapeutic use, or formulation are crucial for enforceability.
  • Patent landscape: Dense patent environments in Canada require thorough FTO analyses to mitigate infringement risks.
  • Strategic positioning: Broad but defensible claims, combined with continuous patent prosecution strategies, enhance market exclusivity.
  • Legal considerations: Claims must meet Canadian patentability standards, emphasizing novelty, inventive step, and utility.
  • Ongoing patent management: Regular portfolio assessment and potential licensing can maximize the patent's value in competitive markets.

FAQs

1. What types of claims are most common in pharmaceutical patents like CA2875824?
Most commonly, pharmaceutical patents include compound claims, use claims, formulation claims, and process claims, each serving to protect different aspects of the invention.

2. How does Canadian patent law differ from other jurisdictions in pharmaceutical patenting?
Canada emphasizes inventive step and utility with a rigorous examination process. It also offers specific provisions, such as the patent linkage mechanism with drug approval processes, which influence patent strategies.

3. How can patent CA2875824 be validated against prior art?
A comprehensive prior art review must be conducted, analyzing previous patents, publications, and proprietary disclosures to ensure claims are novel and non-obvious over existing knowledge.

4. What are the risks of patent infringement in Canada for a drug similar to CA2875824?
The primary risk stems from overlapping claims with existing patents. An FTO analysis helps identify potential infringement threats, informing licensing, design-around strategies, or patent challenges.

5. What strategic considerations are key for maintaining CA2875824’s patent protection?
Maximizing patent lifespan through timely filings, pursuing divisional or continuation patents, extending claims via patent families, and monitoring competitor activity are vital.


References

  1. Canadian Patent Office, Guide to Patentability, 2022.
  2. CIPO Patent Landscape for Pharmaceuticals, 2021.
  3. Canadian Patent Act, R.S.C., 1985, c. P-4.
  4. F. P. Van Dongen, Pharmaceutical Patent Law in Canada, Intellectual Property Journal, 2020.
  5. World Intellectual Property Organization (WIPO), PatentScope Database.

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