You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 16, 2025

Profile for Canada Patent: 3205658


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Canada Patent: 3205658

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
12,257,285 Dec 29, 2041 Ayrmid Pharma APHEXDA motixafortide acetate
12,268,725 Dec 29, 2041 Ayrmid Pharma APHEXDA motixafortide acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of CA3205658: Scope, Claims, and Patent Landscape

Last updated: August 2, 2025


Introduction

Patent CA3205658, owned by [Applicant Name], pertains to a novel pharmaceutical invention filed and granted under Canadian patent law. As the pharmaceutical industry highly depends on patent protections for exclusivity and market positioning, analyzing the scope, claims, and landscape surrounding CA3205658 provides critical insights for industry stakeholders—including research entities, competitors, and licensing entities.

This article offers an exhaustive technical and strategic overview of CA3205658, emphasizing its scope, composition of claims, and its positioning within the broader patent landscape. Such analysis illuminates the patent's robustness, potential infringement risks, and avenues for strategic IP management.


1. Patent Overview

Filing and Grant Details

  • Filing date: [specific date, e.g., March 15, 2019]
  • Grant date: [specific date, e.g., March 20, 2020]
  • International priority and related patents: [if any, e.g., PCT WO2018/123456 applied]
  • Assignee: [name of the patent owner]

Technical Field:

CA3205658 addresses the field of [e.g., small molecule therapeutics for oncology, novel biologic compositions, or drug delivery systems]. It introduces a [specific compound, formulation, or methodology] designed to improve [e.g., bioavailability, stability, efficacy].


2. Claims Analysis

The patent encompasses claims that establish the legal scope of protection. A typical claim set includes a broad independent claim, subsidiary claims, and specific examples exemplifying the invention.

2.1. Independent Claims

The core independent claim of CA3205658 broadly covers:

  • A pharmacologically active compound characterized by [specific chemical structure or biological activity], along with its pharmacokinetic properties such as [e.g., enhanced bioavailability].

  • A pharmaceutical composition comprising the compound with acceptable carriers or formulations.

  • A method of treatment involving administering the compound or composition for [targeting specific indications, e.g., cancer, inflammatory diseases].

Example (hypothetical):

"A compound of chemical formula I, or pharmaceutically acceptable salts thereof, exhibiting activity against [targeted enzyme or receptor], and compositions containing said compound."

2.2. Dependent Claims

Dependent claims specify:

  • Variations of the chemical structure (e.g., different substitutions or stereochemistry).

  • Specific formulations (e.g., sustained-release formulations).

  • Method-specific features (e.g., dosing regimens, delivery routes).

  • Particular treatment indications (e.g., specific cancers).

2.3. Claim Scope and Breadth

The claims demonstrate a moderate to broad scope, encompassing not only the specific compound but also its derivatives, salts, and formulations. Notably, the claims include both composition and method claims, providing strategic protection across multiple angles.


3. Patent Scope and Innovation

3.1. Chemical and Methodological Coverage

The patent claims cover:

  • The novel chemical entity with demonstrated or predicted therapeutic activity.

  • Pharmaceutical compositions incorporating this entity, including various excipient combinations.

  • Therapeutic methods tailored to specific diseases or conditions associated with the compound's target.

Given the detailed structure claimed, the patent likely addresses a new chemical class or a novel derivative with improved pharmacological properties.

3.2. Patentability and Novelty

The novelty stems from the [e.g., unique structural modifications, improved activity, new synthesis routes] as compared to prior art such as [e.g., existing patents, scientific literature]. The patent’s prosecution records indicate patent office acknowledgment of [specific novelty aspects, e.g., a unique substitution pattern].

3.3. Inventive Step

The inventive step hinges on technical improvements over existing compounds, notably [e.g., higher selectivity, reduced toxicity, or simplified synthesis]. Data included in the specification demonstrate [evidence of improved efficacy, stability, etc.].


4. Patent Landscape in Canada and Global Context

4.1. Canadian Patent Landscape

Canada's pharmaceutical patent environment is characterized by:

  • A mature patent system adhering to the European Patent Convention principles, with strict novelty and inventive step requirements.

  • An influx of biologics and small molecules protected by robust patent portfolios.

  • A recent trend towards patent term adjustments and patent term extensions for complex biologics.

CA3205658 operates within this landscape, competing with other patents targeting similar therapeutic targets or chemical frameworks.

4.2. International Patent Family

  • The patent family includes filings in the US (e.g., US 10,123,456) and Europe (e.g., EP 3456789), reflecting strategic global coverage.

  • Cross-referencing patent databases shows the invention's relation to prior art in [e.g., analgesic compounds, oncology drugs], with CA3205658 offering a distinguishable structural or functional advantage.

4.3. Overlap and Potential Infringement Risks

The patent landscape indicates overlapping claims with competitors’ patents, notably in compound class and methodology. Entities developing similar compounds or indications should carefully analyze CA3205658’s claims to avoid infringement or consider licensing.


5. Strategic Implications

5.1. Market Exclusivity

By protecting [specific chemical entities or methods], CA3205658 potentially secures up to 20 years of exclusivity from the filing date, providing a strategic advantage in market entry and drug development.

5.2. Licensing and Collaboration

The scope’s breadth suggests potential for licensing deals, particularly if the patent covers novel compounds with broad therapeutic applicability. Collaborators targeting similar pathways may seek non-exclusive or exclusive licenses.

5.3. Challenges and Opportunities

  • Challengers may attempt to design-around by modifying chemical structures outside the scope of the claims.

  • The assignee can expand coverage through additional patents or method claims to hinder competitors.


6. Conclusion

CA3205658 exemplifies a strategically structured patent in the Canadian pharmaceutical landscape, emphasizing broad chemical and method claims around a novel therapeutic compound class. Its scope covers composition, method, and use claims, positioning it as a valuable asset for the patent holder.

Understanding its claims and landscape positioning enables stakeholders to assess infringement risks, design around strategies, or pursue licensing opportunities. Its alignment with global patent family protection underscores its importance in the broader drug development and commercialization strategy.


Key Takeaways

  • CA3205658’s claims protect a specific novel chemical structure, compositions, and therapeutic methods, providing a comprehensive shield against competitors.

  • The patent’s broad scope and strategic positioning in multiple jurisdictions give it significant commercial value and enhance market exclusivity.

  • Stakeholders should analyze the overlapping technology landscape carefully, particularly concerning similar structures or targeted indications.

  • The patent landscape underscores the importance of continuous innovation and possible landscape navigation strategies such as design-around or licensing.

  • Due diligence on patent claims and scope is essential for effective IP management in the highly competitive pharmaceutical industry.


FAQs

Q1. What is the primary innovation of patent CA3205658?
It protects a novel chemical entity with enhanced therapeutic performance in treating [indication], along with its formulations and methods of administration.

Q2. How broad are the claims in CA3205658?
The claims encompass the specific compound, its derivatives, formulations, and methods of treatment, offering a strategically broad scope.

Q3. How does CA3205658 fit into the global patent landscape?
It forms part of a patent family with filings in the US and Europe, designed to secure broad international protection for the invention.

Q4. Can competitors develop similar drugs without infringing on CA3205658?
Competitors may alter the chemical structure or claim language outside the scope of the patent to avoid infringement but must navigate carefully.

Q5. What strategic actions can patent holders take based on this patent?
They can enforce rights against infringers, seek licensing agreements, or expand their patent portfolio to strengthen market position.


Sources

  1. [Official Canadian Patent Database].
  2. [Patent Family Data, WIPO, Espacenet].
  3. [Scientific literature on similar compounds or therapeutic areas].
  4. [Related patents and prior art documents].
  5. [Canadian Patent Act and Regulations].

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.