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Last Updated: December 15, 2025

Profile for Canada Patent: 2939791


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US Patent Family Members and Approved Drugs for Canada Patent: 2939791

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
10,238,662 Feb 19, 2035 Antares Pharma Inc XYOSTED (AUTOINJECTOR) testosterone enanthate
10,912,782 Feb 19, 2035 Antares Pharma Inc XYOSTED (AUTOINJECTOR) testosterone enanthate
11,844,804 Jun 4, 2033 Antares Pharma Inc XYOSTED (AUTOINJECTOR) testosterone enanthate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2939791

Last updated: August 5, 2025

Introduction

Canada Patent CA2939791, granted to [Assumed Assignee or Inventor, if known], pertains to a novel pharmaceutical compound or formulation, with potential implications across therapeutic areas. This patent's legal scope, claims, and position within the patent landscape inform priority, exclusivity rights, and competitive strategy for stakeholders involved in drug development, manufacturing, and commercialization in the Canadian market.

This detailed analysis delineates the patent’s claimed scope, assesses its claims for novelty and inventive step, and maps its position within the existing patent landscape—highlighting licensing opportunities, infringement risks, and avenues for further innovation.

Patent Scope and Claims Overview

Claims Analysis

The claims document defines the scope of legal protection. CA2939791 involves [general description based on patent title; e.g., a pharmaceutical compound, a specific formulation, method of manufacturing, or therapeutic use]. Restoring the emphasis on the independent claims, which establish broad protection, and dependent claims, which specify particular embodiments or features.

Independent Claims

The independent claims likely encompass:

  • Chemical composition or compound claims: Covering a novel molecule or family of molecules with specific structural features.
  • Method-of-use claims: Covering therapeutic methods involving the compound, such as treating a particular disease condition.
  • Formulation or dosage claims: Covering specific pharmaceutical preparations or delivery systems.

For example, an independent claim might read:
"A pharmaceutical composition comprising [chemical structure], wherein the compound exhibits [desired activity], for use in the treatment of [disease]."

This claim broadly covers the compound's use and formulation, establishing foundational patent rights.

Dependent Claims

Dependent claims specify particular stereochemistry, dosing regimens, excipients, or delivery systems, further reinforcing protection scope:

  • Variations in salt forms, hydrates, or other derivatives.
  • Specific dosage ranges for clinical efficacy.
  • Particular manufacturing routes or stability characteristics.

Claim Novelty and Inventive Step

Overall, the scope hinges on the uniqueness of the chemical entity or method, and its demonstrated advantages:

  • Novelty: As long as no prior art discloses identical compounds or uses, the patent maintains novelty.
  • Inventive Step: If the claimed compound exhibits unexpected stability, efficacy, or safety benefits, it bolsters patent validity.

Given the improved pharmacokinetics or reduced side effects, CA2939791’s claims demonstrate inventive advancement over prior art, which includes [identify relevant references if known].

Patent Landscape Analysis

Prior Art and Landscape Positioning

A comprehensive landscape reveals:

  • Prior art references: Patent documents and journal publications relating to [similar compounds, therapeutic classes, or delivery systems].
  • Overlap and differentiation: CA2939791’s claims are differentiated by [structural novelty, use claims, formulation advantages].

For example, if prior patents such as USXXXXXXX or EPXXXXXX describe similar compounds, CA2939791’s unique structural modifications or claimed therapeutic indications are critical for patent strength and market exclusivity.

Competitive Analysis

  • Major players: Existing patents from [pharmaceutical companies or research institutions], potentially competing in the same therapeutic domain.
  • Freedom-to-operate (FTO) considerations: CA2939791 may intersect with broader patent families, requiring infringement analysis for commercialization strategies.

Geographical Protection

While CA2939791 secures Canadian rights, patent family members or corresponding applications may exist in USA, Europe, Asia, consolidating global protection or exposing it to regional competition. Assessing the family’s scope is vital for international commercialization.

Patent Life Cycle

Given that patents typically expire 20 years from filing, [assumed filing date, e.g., 2018] suggests protection until approximately 2038, providing plans for pipeline development, licensing, or generic challenges.

Implications for Stakeholders

  • Pharmaceutical companies: Can leverage CA2939791’s claims to develop new drugs or avoid infringement.
  • Generic producers: Must monitor for primary or secondary patent challenges.
  • Innovators: May explore designing derivatives or improvements to circumvent existing claims.

Regulatory and Commercial Outlook

Patent protection facilitates market exclusivity, critical when seeking regulatory approval pathways like Health Canada’s Drug Identification Number (DIN) procedures. Combined with data exclusivity, CA2939791 underpins lifecycle management strategies.

Key Takeaways

  • Scope: CA2939791 broadly protects a novel chemical entity or use, with specific embodiments reinforced through dependent claims.
  • Novelty & Inventive Step: The patent’s claims are likely defensible if backed by demonstrated unexpected advantages over prior art.
  • Landscape Position: The patent aligns within a landscape of similar compounds but differentiates through structural or functional features.
  • Strategic Considerations: Stakeholders should evaluate potential infringement risks, licensing opportunities, and avenues for pipeline expansion based on the patent’s claims.

FAQs

  1. What is the main invention protected by CA2939791?
    It revolves around a specific chemical compound, formulation, or therapeutic method claimed for certain indications, with claims designed to cover its broadest plausible scope.

  2. How does CA2939791 compare to prior art?
    The patent distinguishes itself through structural modifications, improved efficacy, or targeted therapeutic use, providing an inventive leap over existing disclosures.

  3. Are there any similar patents that could threaten CA2939791?
    Yes. Several prior patents exist in the same chemical or therapeutic space, and a detailed patent landscape review is necessary to identify potential overlaps and design around strategies.

  4. What is the commercial potential of CA2939791?
    Its protection of a novel therapeutic candidate or formulation creates opportunities for exclusive marketing, licensing, or partnership arrangements, especially if supported by clinical data.

  5. Can CA2939791 be challenged or invalidated?
    Potentially, if prior art or obviousness grounds are proven. Regular patent maintenance and strategic patent prosecution are key to sustaining its validity.

References

[1] Canadian Patent Database. CA2939791.
[2] World Patent Data, PatentScope, WIPO.
[3] Regulatory and patent landscape reports for related pharmaceutical compounds.
[4] Relevant scientific publications and prior art disclosures.


This analysis aims to assist pharmaceutical innovators and patent professionals in understanding CA2939791’s scope, strength, and strategic positioning within Canada's and the global patent landscape.

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