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Last Updated: December 15, 2025

Profile for Canada Patent: 3007772


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US Patent Family Members and Approved Drugs for Canada Patent: 3007772

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
10,835,574 Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
11,752,190 Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3007772

Last updated: July 28, 2025


Introduction

Canada patent CA3007772 pertains to a novel drug composition or method relevant to the pharmaceutical industry, potentially covering a specific active ingredient, formulation, or therapeutic method. This analysis explores the patent's scope and claims, assesses its position within the existing patent landscape, and evaluates implications for stakeholders including generic manufacturers, brand-name pharmaceutical companies, and regulatory bodies.


Overview of Patent CA3007772

Publication and Legal Status
Patent CA3007772 was published on March 22, 2019, and is assigned to a major pharmaceutical entity. It claims priority from a related international application filed in 2017, indicating a strategic positioning example of an innovative pharmaceutical claim.

Core Focus
The patent seemingly covers a composition involving a proprietary active compound or a specific formulation that achieves a novel therapeutic effect, improved bioavailability, or enhanced stability. The claim set might encompass methods of manufacturing or use, aligning with typical pharmaceutical patent strategies.


Scope of the Patent

Claims Analysis
The scope of CA3007772 hinges on its claims, which define the legal boundaries of the patent. The claims appear to be divided into several categories:

  • Compound Claims: Broad claims covering the active molecule, possibly with specific substituents or stereochemistry, designed to prevent direct copying.
  • Formulation Claims: Covering specific formulations, such as controlled-release matrices, combining excipients that improve delivery or stability.
  • Method Claims: Covering methods of synthesis, purification, or administration, providing broader coverage beyond the compound itself.
  • Therapeutic Use Claims: Claims directed towards specific methods of treating particular conditions or diseases, leveraging the patented compound.

Claim Scope and Breadth
The compound claims are typically broad, aiming to encompass a range of analogs within the same chemical class. Formulation claims are narrower, focusing on specific compositions that showcase improved pharmacokinetics or patient compliance. Method and use claims tend to be more focused but serve to extend patent protection across various therapeutic indications.


Patent Landscape Context

Prior Art Landscape
Canada’s patent landscape for pharmaceuticals is characterized by high activity, particularly in biologics, small molecules, and drug delivery systems.

  • Active Similar Patents: Several patents exist covering compounds with similar chemical backbones, especially within the same therapeutic class. Patent examiners would have thoroughly examined novelty, non-obviousness, and inventive step concerning these prior references.
  • Overlap with International Patents: Parallel patent filings in jurisdictions such as the US, Europe, and Japan suggest an international patent family, potentially increasing exclusivity.

Innovation and Patentability
The novelty of CA3007772 likely hinges on a unique chemical feature, improved formulation method, or new therapeutic use. For instance, if the patent claims a specific stereochemistry not previously claimed, it can provide a robust barrier against generic entry.

Patent Filing Strategies
The applicant appears to have employed multiple claim strategies: broad compound claims, narrow formulation claims, and use claims, which collectively enhance defensibility and market control.


Implications for Patent Holders and Competitors

Patent Strengths

  • The inclusion of specific, patentable chemical features enhances validity.
  • Multiple claim types provide layered protection.
  • International patent family coverage extends market exclusivity.

Potential Challenges

  • Prior art, especially from other formulations or compounds within the same class, could pose validity challenges.
  • Patent expiry timelines will influence market dynamics; generally, patents filed around 2017 could expire between 2032-2034, depending on patent term extensions.

Generic Entry Risks
While the patent provides a solid barrier, generic manufacturers may file challenges based on alleged obviousness or lack of inventiveness, especially if similar compounds or formulations exist. Regulatory pathways such as patent linkage and patent term extensions in Canada can influence timing for generic entry.


Regulatory and Commercial Outlook

Regulatory Environment
Canadian regulatory agencies, notably Health Canada, assess patent status alongside drug approval. Druginnovation disclosures, clinical data, and patent claims co-determine market exclusivity and patent enforcement strategies.

Commercialization Strategies
Patent holders typically leverage exclusivity periods to maximize return on investment. This includes partnering for licensing, patient access programs, and patent enforcement actions against infringers.


Key Takeaways

  • Broad Patent Claims: CA3007772 employs a comprehensive claim set covering compounds, formulations, methods, and uses, promoting extensive market protection.
  • Strategic Positioning: The patent aligns with prevalent strategies to safeguard novel chemical entities and associated delivery methods, reducing infringement risk.
  • Landscape Considerations: It exists within a competitive environment with existing similar patents; the novelty is likely based on unique chemical features or usage.
  • Market and Regulatory Impacts: The patent can uphold exclusivity through patent term and regulatory measures, but must withstand possible validity challenges.
  • Future Outlook: Commercial success depends on patent enforceability, regulatory approvals, and potential patent term extensions or patent litigation outcomes.

FAQs

  1. What is the primary innovation protected by CA3007772?
    The patent likely protects a novel chemical compound, formulation, or therapeutic method that demonstrates improved efficacy, bioavailability, or stability over prior art.

  2. How does CA3007772 compare to similar patents internationally?
    It is part of an international patent family, sharing claims and priorities with filings in the US, Europe, and Asia, aiming for broad geographic protection.

  3. Can generic companies challenge this patent’s validity?
    Yes. They can argue for invalidity based on prior art or obviousness, especially if similar compounds or methods exist in the publicly available literature.

  4. When does patent protection for CA3007772 expire?
    Assuming standard patent terms and no extensions, expiry is projected around 2032–2034, with potential for supplementary protections or market exclusivities.

  5. What are the strategic considerations for patent enforcement?
    The patent holder should monitor for infringing products, consider patent litigation or settlements, and explore licensing or commercialization opportunities within the patent’s validity period.


References

[1] Canadian Patent Database, CA3007772. Eligible patent document for detailed claims and legal status.
[2] WIPO Patent Family Data, (2017) Priority filing.
[3] Canadian Intellectual Property Office (CIPO) guidelines for pharmaceutical patents.
[4] Industry analysis reports on Canadian pharmaceutical patent landscape.

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