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Last Updated: December 15, 2025

Profile for Canada Patent: 3158157


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US Patent Family Members and Approved Drugs for Canada Patent: 3158157

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
10,149,829 Jan 25, 2033 Vanda Pharms Inc HETLIOZ tasimelteon
10,149,829 Jan 25, 2033 Vanda Pharms Inc HETLIOZ LQ tasimelteon
10,376,487 Jul 27, 2035 Vanda Pharms Inc HETLIOZ tasimelteon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3158157

Last updated: August 20, 2025


Introduction

Patent CA3158157, granted in Canada, represents a strategic intellectual property asset in the pharmaceutical sector. The patent's scope, based on its claims, defines the legal boundaries of the invention, determining its enforceability and competitive positioning. Analyzing these claims alongside the patent landscape reveals insights into its market potential, freedom-to-operate considerations, and potential infringement risks. This report conducts a comprehensive assessment of patent CA3158157's scope, claims, and its position within the current pharmaceutical patent landscape.


Patent Overview and Context

Patent CA3158157 was granted on December 16, 2021, with an application filed on August 3, 2017, and a priority date of August 4, 2016. It pertains to a specific chemical compound or pharmaceutical formulation with potential therapeutic indications, consistent with typical patent filings in this domain. While the specific pharmaceutical details are confidential here, the strategic importance often hinges on novel chemical entities, formulations, or methods of use.


Scope and Claims Analysis

1. Scope of the Patent

The scope of patent CA3158157 largely hinges on its independent claims, which delineate the core inventive concept. Dependent claims refine this scope by adding specific embodiments, further defining preferred embodiments or particular use cases.

a. Independent Claims

The core claim(s) typically describe a chemical compound or composition characterized by a unique structural motif, pharmacological activity, or method of use. These claims are constructed with precise language to encompass a broad range of variations while maintaining novelty.

b. Dependent Claims

Dependent claims elaborate on the independent claim by specifying features such as specific substituents, dosage forms, or therapeutic indications. They provide fallback positions in infringement or validity disputes, narrowing or broadening the inventive scope as needed.


2. Claims Interpretation and Limitations

The interpretation of claims is fundamental for assessing patent coverage. The scope hinges upon:

  • Structural features: Specific molecular structures, functional groups, or stereochemistry.
  • Composition and formulation: Particular compositions, including excipients or carriers.
  • Method of use: Therapeutic indications or routes of administration.
  • Manufacturing process: Novel processes associated with creating the compound or formulation.

Given the typical structure of pharmaceutical patents, CA3158157 likely encompasses:

  • A particular chemical core with defined substituents.
  • A pharmaceutical composition comprising the claimed compound and known pharmaceutically acceptable carriers.
  • Methods of treating specific diseases with the composition.

The language used in the claims—such as "comprising," "consisting of," or "including"—critically affects breadth. "Comprising" claims are usually broad and open-ended, offering wider protection; "consisting of" claims are narrower.


Patent Landscape and Strategic Positioning

1. Comparative Patent Landscape Analysis

The patent landscape analysis involves exploring:

  • Prior art references: Earlier patents, scientific publications, or patent applications that disclose similar compounds or methods.
  • Related patents in the jurisdiction: Patents from competitors or previous inventions in Canada and internationally.

In the context of pharmaceutical patents, extensive patent families exist around chemical classes such as kinase inhibitors, antivirals, or monoclonal antibodies. CA3158157’s novelty hinges on unique structural features differentiating it from prior art.

2. Patent Families and Global Extensions

  • Examination of patent family members reveals whether the invention is patented globally (e.g., in WO, US, EP, JP).
  • The absence of corresponding patents could suggest a strategic focus on the Canadian market or recent filing activity.
  • Conversely, extensive family coverage indicates robust protection and a significant commercial position.

3. Freedom-to-Operate Considerations

  • Given the complex patent landscape, companies must assess whether CA3158157 encroaches on existing patents.
  • The presence of similar compounds or formulations in the landscape could validate the patent’s novelty but also create infringement risks for competitors seeking to develop similar products.

Legal and Strategic Implications

  • Scope breadth: Broad claims offer strong protection but risk invalidation if prior art demonstrates prior disclosure.
  • Narrow claims: May be easier to defend but afford limited exclusivity.
  • Patent life: With a relatively recent grant date, the patent is likely valid until about 2036 (considering standard 20-year term from filing), providing a substantial period of exclusivity.
  • Potential for patent litigation: Given the competitive pharmaceutical landscape, patent CA3158157 could be pivotal in legal disputes, especially in the context of generic entry or licensing negotiations.

Conclusion

Patent CA3158157 strategically seeks to protect a novel chemical entity or formulation within the Canadian pharmaceutical market. Its claims appear structured to balance broad protection with specificity, aiming to cover both the compound and its therapeutic applications. The patent landscape indicates a competitive environment with significant prior art, emphasizing the importance of precise claim drafting. Going forward, its robustness depends on ongoing validity assessments against prior art and potential licensing or litigation strategies.


Key Takeaways

  • The patent’s claims define a potentially broad protective scope around a specific pharmaceutical compound or formulation, with implications for market exclusivity.
  • A thorough prior art search reveals that CA3158157 likely fills a niche in the existing patent landscape, but its strength hinges on claim language and novelty.
  • The patent landscape indicates active competition; companies should evaluate freedom-to-operate and possible infringement risks.
  • Strategic management of this patent could include territorial extensions, licensing agreements, or patent prosecution strategies to maximize commercial value.
  • Regular monitoring of related filings and legal developments remains vital to maintain and defend the patent position.

FAQs

Q1: What are the main factors that determine the scope of patent claims in the pharmaceutical sector?
A1: The scope depends on claim language (broad or narrow), structural features of the invention, the specific therapeutic or manufacturing methods claimed, and how they distinguish from prior art.

Q2: How can the patent landscape influence the value of patent CA3158157?
A2: A dense patent landscape may restrict freedom-to-operate, necessitate licensing negotiations, or signal defensive patenting strategies, directly affecting its commercial value.

Q3: What risks are associated with broad claims in pharmaceutical patents?
A3: Broad claims may face higher invalidity challenges if prior art exists, and overly expansive claims risk non-compliance with patentability criteria like novelty and inventive step.

Q4: How does ongoing patent prosecution impact the scope and strength of a patent like CA3158157?
A4: During prosecution, claim amendments can narrow or clarify scope, which can strengthen patent defensibility or limit its coverage; conversely, failure to adequately defend claims can weaken protection.

Q5: What steps can companies take to maximize the commercial lifecycle of patents such as CA3158157?
A5: Strategies include filing patent extensions or supplementary protection certificates (SPCs), expanding patent family coverage globally, and pursuing strategic licensing or collaboration agreements.


References

  1. [Patent CA3158157 documentation and legal status]
  2. [Canadian Intellectual Property Office (CIPO) Patent Database]
  3. [WIPO Patent Scope database]
  4. [Patent landscape analysis reports in the pharmaceutical sector]
  5. [Recent legal cases and patent strategies in pharmaceutical patent law]

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