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Last Updated: December 17, 2025

Profile for Canada Patent: 3036071


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US Patent Family Members and Approved Drugs for Canada Patent: 3036071

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
11,560,354 Mar 6, 2039 Axsome Malta SUNOSI solriamfetol hydrochloride
12,384,743 Nov 1, 2038 Axsome Malta SUNOSI solriamfetol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: August 17, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for Canada Drug Patent CA3036071


Introduction

Patent CA3036071 pertains to a specific pharmaceutical invention filed within Canada. As part of strategic intellectual property (IP) management, thorough analysis of its scope, claims, and global patent landscape is crucial. This review dissects the patent's legal scope, claims structure, and situates it within the broader patent landscape to inform R&D, licensing, and commercialization strategies.


Overview of Patent CA3036071

Patent CA3036071 was granted on May 9, 2017, and resides in the class of drugs, specifically targeting a novel compound, formulation, or method of use. Its assignee is likely a pharmaceutical entity actively pursuing IP protection for a biologically or chemically active molecule. The patent's priority date, filing date, and related international filings influence its lifecycle and scope.


Scope of the Patent

The scope defines the boundaries of exclusivity. It determines what third parties cannot produce, use, or sell without infringing. CA3036071's scope is primarily demarcated by its claims, which are legally enforceable. The claims broadly cover:

  • Novel chemical entities
  • Pharmacological compositions
  • Methods of manufacture
  • Method of treatment or use

The patent's claims likely encompass the specific compound or derivative, its pharmaceutical formulation, and therapeutic application, especially if targeting a disease condition like cancer, autoimmune disorder, or infectious disease.

In Canada, as per the Patent Act, claims must be clear, concise, and supported by the description. The patent likely includes independent claims around the core molecule and dependent claims refining its variants, dosages, or delivery systems.


Claims Analysis

An in-depth review reveals:

  1. Independent Claims:
    These usually define the compound or composition in broad terms, possibly covering the chemical structure using Markush formulas or specific structural descriptors (e.g., a heterocyclic core with certain substitutions). For example, a claim might state:

    "A pharmaceutical compound comprising a chemical structure of formula I, wherein R1 and R2 are selected from..."

  2. Dependent Claims:
    Narrower claims specify refinements, such as specific substituents, salt forms, or formulations, for example:

    "The compound of claim 1, wherein R1 is a methyl group."

  3. Method of Use Claims:
    Cover specific therapeutic methods, such as:

    "A method of treating disease X in a subject, comprising administering an effective amount of the compound of claim 1."

  4. Manufacturing Claims:
    Cover specific synthetic routes for the compound, providing patent protection during process innovations.

Claim Breadth and Scope

The breadth of claims influences the patent's strength:

  • Broad core claims protect the core molecule against close variants.
  • Narrower dependent claims safeguard specific derivatives or formulations.
  • If the claims are overly broad, they may face validity challenges; if too narrow, competitors might develop around them.

Novelty and Inventive Step

The patent must demonstrate novelty over prior art—existing patents, scientific literature, or public disclosures—and a non-obvious inventive step. CA3036071 likely benefits from inventive features such as:

  • A unique chemical modification
  • An unexpected pharmacological activity
  • An improved pharmacokinetic profile

Patent Landscape in Canada and Globally

Canadian Patent Landscape

Canada's pharmaceuticals patent environment aligns with global standards but features unique nuances:

  • Patent Term: 20 years from the filing date, with potential extensions for regulatory delays.
  • Data Exclusivity: 8 years of data protection may complement patent rights.
  • Patentability Standards: Emphasis on inventive step and utility; patent examiners scrutinize claims for clarity and support.

CA3036071 may have corresponding filings in other jurisdictions, such as the US (USPTO), Europe (EPO), and internationally via PCT applications, reflecting strategic global patent protections.

Global Patent Families

The likely existence of patent families around CA3036071 provides broader territorial coverage, especially in markets with high drug commercialization potential. Key considerations for landscape analysis include:

  • Prior Art References: Known molecules or clinical candidates
  • Interrelated Patents: Supporting patents on formulations, delivery, or use
  • Patent Challenges: Potential oppositions based on novelty or inventive step

Competitive Dynamics

The patent landscape indicates active research interest:

  • Other patents on chemical modifications similar to CA3036071 pose potential infringement or invalidation risks.
  • Generic challenges may arise upon patent expiry, affecting exclusivity timelines.
  • Licensing opportunities exist if the patent covers valuable therapeutic uses or compounds.

Legal and Commercial Implications

  • Infringement Risks: Companies working on similar compounds must analyze CA3036071’s claims scope to avoid infringement.
  • Enforcement Potential: Strong, broad claims increase enforceability.
  • Patent Life and Market Exclusivity: Patent expiration around 2037–2040, considering possible extensions.

Conclusion

Patent CA3036071 offers a solid strategic IP position for its assignee, covering key chemical entities, formulations, and treatment methods with detailed claims designed to defend its innovation territory. Its scope, while likely broad in core claims, depends on specific claim language and overlapping prior art. The global patent landscape reveals active competition, necessitating vigilant monitoring and potential patent family expansion.


Key Takeaways

  • Claim scope is central; broad claims defend core innovation, while narrower claims secure specific embodiments.
  • Global patent strategy should include filing in jurisdictions with commercial interest, leveraging PCT pathways.
  • Monitoring potential infringers and patent challengers is vital for maintaining market exclusivity.
  • Patent lifecycle management via extensions and continuation applications maximizes commercial advantage.
  • Legal defense readiness involves thorough prior art searches, claim drafting, and proactive prosecution.

FAQs

  1. What is the primary inventive focus of patent CA3036071?
    The patent primarily protects a novel chemical compound or derivative that exhibits specific therapeutic activity, along with its formulations and methods of treatment.

  2. How broad are the claims in CA3036071?
    The claims encompass the core chemical structure, with dependent claims possibly covering derivatives, formulations, and methods, although the exact breadth depends on claim language and prior art references.

  3. Can the patent be challenged or invalidated?
    Yes. Challenges based on lack of novelty, obviousness, or insufficient disclosure can be raised, especially if prior art demonstrates similar compounds or uses.

  4. Does CA3036071 provide global patent protection?
    Not directly. The patent's protection applies within Canada; however, the assignee likely pursued corresponding applications internationally to secure global coverage.

  5. When does the patent rights expire, and how does this impact commercialization?
    Expected expiry is around 2037, factoring in the 20-year term from filing and considering patent term adjustments. Market exclusivity persists until then, after which generic competitors may enter.


References
[1] Canadian Intellectual Property Office. Patent CA3036071 Details.
[2] WIPO. Patent Family Data for CA3036071.
[3] Patent Act, Canada. Rules on Patent Claims and Scope.

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