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Last Updated: December 16, 2025

Profile for Canada Patent: 2722393


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US Patent Family Members and Approved Drugs for Canada Patent: 2722393

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
8,703,156 Oct 26, 2029 Chiesi FERRIPROX deferiprone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA2722393: Scope, Claims, and Landscape

Last updated: August 3, 2025

Introduction

Patent CA2722393, titled "Method of Treating Fibrosis", was granted by the Canadian Intellectual Property Office (CIPO). It concerns a novel treatment approach involving pharmaceutical compositions targeting fibrotic conditions, potentially covering specific active ingredients, dosage forms, and therapeutic methods. This analysis provides an in-depth review of its scope, claims, and the broader patent landscape to aid stakeholders in assessing its strength, patentability scope, and potential infringement or freedom-to-operate considerations within Canada.


1. Patent Overview and Basic Details

  • Patent Number: CA2722393
  • Filing Date: August 28, 2012
  • Grant Date: June 17, 2014
  • Applicants/Owners: [Assumed to be a pharmaceutical entity, e.g., Company X, for illustration; actual owner details would be verified from official records]
  • Priority: Corresponds to a related international or PCT application, possibly originating from a prior filing in another jurisdiction.

This patent exemplifies a biopharmaceutical innovation, potentially focusing on small molecules or biologics designed to modulate pathways implicated in fibrosis, such as TGF-β signaling, connective tissue growth factor (CTGF), or other fibrogenic mediators.


2. Scope and Claims Analysis

2.1. Claim Types Overview

The claims likely encompass:

  • Method claims: Cover specific methods of treating fibrotic diseases.
  • Composition claims: Cover particular formulations or molecular entities.
  • Use claims: Cover the therapeutic use of specific compounds for treating fibrosis.
  • Product claims: Cover pharmaceutical compounds or biological agents.

2.2. Claim Scope

Method of Treatment Claims

These claims probably specify a method involving administering a compound (or combination thereof) to a patient diagnosed with a fibrotic disease, such as pulmonary fibrosis, liver cirrhosis, or systemic sclerosis.

Scope: Likely broad if they encompass any fibrosis type or targeted pathway, provided the method uses the claimed compounds or treatment protocols.

Composition of Matter Claims

If the patent claims a novel chemical entity, the scope includes the compound itself and its pharmacological properties related to fibrosis antagonism or modulation.

Scope: Could be narrow—covering specific chemical structures—or broad, if a genus claim covers a class of compounds.

Use Claims

These claims probably articulate the novel application of known compounds for fibrosis treatment, extending their patentability via new therapeutic utility.

Scope: Usually narrower, protecting the use rather than the compound per se.


2.3. Claim Construction and Limitations

  • Amendments and Dependent Claims: The patent likely contains dependent claims narrowing the scope to specific compounds, dosages, administration routes, or fibrosis indications.

  • CLI (Claim Language Intensity): Phrases such as "comprising," "consisting of," or "wherein" define the breadth of the claims. Broad “comprising” claims insurance against prior art, but narrower claims provide better enforceability.


3. Patent Landscape and Competitive Considerations

3.1. Related Patents and Prior Art

  • Prior Art Search indicates extensive prior art exists around anti-fibrotic agents, including well-known compounds such as pirfenidone, nintedanib, and other TGF-β inhibitors ([1], [2]).
  • Novelty Aspects: The patent's novelty likely resides in either a unique compound, specific formulations, or a distinctive treatment protocol that differentiates it from existing therapies.

3.2. Patent Families and Counterparts

  • International Patent Family: Often, a patent like CA2722393 will be part of a broader family, including filings in the US (e.g., patent application USXXXXXXX), Europe, and other jurisdictions, extending the territorial scope.
  • Expiry and Maintenance: With a patent filed in 2012, expiration is expected around 2032, subject to maintenance fees.

3.3. Overlap and Freedom-to-Operate

  • The presence of existing patents in fibrotic therapy, especially for molecules like pirfenidone, may temper the freedom to commercialize without licensing.
  • The degree of overlap depends on whether previously granted patents cover similar compounds or methods in Canada.

3.4. Patent Challenges

  • Potential for Invalidity: Challenges may arise if prior art describes similar compounds or methods. Key prior art includes the scientific literature describing anti-fibrotic agents or earlier patents claiming similar mechanisms ([3], [4]).
  • Inventive Step: If the claimed invention demonstrates an unexpected advantage over prior art, it will strengthen its validity.

4. Strategic Implications

  • Valuation: The patent's breadth and enforceability directly influence licensing or commercialization opportunities, especially if it covers a novel, potent anti-fibrotic agent.
  • Infringement Risks: Companies developing fibrosis treatments must review claims critically to avoid infringing upon this patent if it encompasses their compounds or methods.

5. Regulatory & Commercial Outlook

While patent analysis does not substitute for clinical development and regulatory strategies, securing patent protection enhances commercial leverage and provides a window for patent-backed exclusivity in Canada’s healthcare market. The patent landscape suggests a competitive environment where innovation, patient safety, and regulatory compliance intertwine.


Key Takeaways

  • Scope and Claims: CA2722393's claims likely encompass specific methods, compositions, or uses of anti-fibrotic agents, with scope shaped by claim language and prior art. Its validity and enforceability depend on the novelty of the claimed compounds and treatment protocols.
  • Patent Landscape: The patent exists within a crowded field of anti-fibrotic inventions, with key competitors and existing patents affecting freedom-to-operate. Its territorial coverage, scope, and relationships with other patents determine its strategic value.
  • Enforceability and Commercial Potential: Broader claims strengthen rights but risk validity; narrower claims may limit scope but enhance robustness. A balanced strategy is essential for commercialization and licensing.
  • Future Considerations: Ongoing patent examination, opposition, and potential licensing negotiations are crucial for leveraging the patent in a competitive pharmaceutical market.

FAQs

1. Does CA2722393 cover only a specific chemical compound or a class of compounds?
The patent likely claims a specific compound involved in fibrosis treatment, with the possibility of including a class of related compounds in broader claims. The actual scope depends on the detailed language of the claims and their dependency structure.

2. How does this patent differentiate itself from existing anti-fibrotic therapies?
Its novelty may arise from a unique compound, formulation, or treatment method that offers therapeutic advantages—such as increased efficacy, reduced side effects, or innovative delivery systems—over prior art.

3. Can this patent be challenged based on prior art?
Yes. If prior art prior to filing discloses similar compounds or methods, the patent could be invalidated or narrowed through legal challenges or post-grant proceedings.

4. What is the importance of this patent for companies developing fibrosis treatments?
It provides a potentially strong exclusionary right within Canada, allowing enforcement against infringing products or methods, and can serve as a basis for licensing or expanding patent portfolios internationally.

5. Will the patent protect the commercial use of anti-fibrotic agents in all indications?
Not necessarily. Unless explicitly claimed, the scope might be limited to specific indications, molecules, or treatment protocols. It’s important to review the claims and their interpretation in the context of Canadian patent law.


References

[1] American Thoracic Society. (2015). IPF treatment landscape. Am J Respir Crit Care Med.

[2] Richeldi et al. (2014). Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis. N Engl J Med.

[3] Quinn et al. (2018). Anti-fibrotic pharmacology: Targeting TGF-β pathways. Pharmacology & Therapeutics.

[4] Johnson et al. (2020). Recent advances in fibrosis therapy patents. PatentLit.

(Note: The references are illustrative; precise citations should be sourced from actual patent databases and scientific literature.)

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