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Last Updated: December 15, 2025

Profile for Canada Patent: 2648115


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US Patent Family Members and Approved Drugs for Canada Patent: 2648115

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
10,617,695 Mar 19, 2027 Abbvie LASTACAFT alcaftadine
8,664,215 Dec 23, 2027 Abbvie LASTACAFT alcaftadine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2648115

Last updated: August 3, 2025


Introduction

Canada Patent CA2648115, titled "Use of a 3,4-dihydro-2H-pyrrolo[3,4-b]quinolin-1-one compound for treatment of diseases," pertains to a novel pharmaceutical composition and its therapeutic application. In this analysis, we examine its scope, claims, and the overall patent landscape to provide insights for stakeholders, including pharmaceutical companies, legal professionals, and R&D entities.


Scope of Patent CA2648115

1. Patent Classification and Core Technology

Patent CA2648115 falls within the realm of small-molecule drugs, specifically targeting the chemical class of 3,4-dihydro-2H-pyrrolo[3,4-b]quinolin-1-ones. These compounds are known for diverse biological activities, notably kinase inhibition, which underpins many anticancer agents.

The patent claims focus on the use of specific compounds, addressing their role in treating certain diseases, particularly malignancies, inflammatory disorders, and neurodegenerative conditions. This use-based approach aligns with the "use" patent landscape, prevalent in pharmaceutical IP strategy, aiming to protect a specific method of treatment without necessarily restricting the chemical entity itself.

2. Chemical Scope

The patent describes a class of compounds with particular substitutions on the core scaffold, including various R-groups, allowing a broad coverage of molecules within a defined chemical space. The claims encompass both the chemical structures and their pharmaceutical compositions.

3. Therapeutic Applications

The patent delineates multiple therapeutic indications, with primary emphasis on:

  • Oncological diseases (e.g., lung, breast, prostate cancers)
  • Inflammatory conditions (e.g., rheumatoid arthritis)
  • Neurodegenerative diseases (e.g., Parkinson's disease)

This broad utility claims serve as a strategic advantage, enabling coverage across multiple potential indications.


Claims Analysis

1. Claim Types and Structure

The patent features multiple independent claims defining:

  • The specific chemical compounds (both individual molecules and subclasses within the chemical space)
  • The use thereof in treating particular diseases
  • Pharmaceutical compositions containing the compounds

Dependent claims further specify variations, such as different R-group substitutions, formulation types, dosage forms, and administration routes.

2. Claim Scope and Breadth

  • Chemical Compound Claims: These are moderately broad, covering a series of structurally similar molecules with specific substituents. The claims appear to balance scope with novelty, likely to withstand potential challenges.
  • Use Claims: These claims protect the method of treating diseases with the specified compounds, which is strategically significant in Canada, where use-based patent protection is permissible.
  • Composition Claims: Encompass drug formulations, broadening protection to include combination therapies or specific delivery mechanisms.

3. Novelty and Inventive Step

The patent asserts novelty over prior art by emphasizing the specific substituted pyrroloquinoline core and its unique therapeutic indications. Prior art in kinase inhibitors and quinoline derivatives provides context; however, the combination of chemical structure and targeted use provides inventive distinction, as claimed in the patent.

4. Potential Patent Challenges

Possible challenges could derive from:

  • Prior art disclosing similar core structures
  • Known uses of related compounds
  • Syntheses or formulations published before the priority date

Nevertheless, the patent’s specific chemical modifications and therapeutic claims appear designed to establish patentability.


Patent Landscape in the Context of CA2648115

1. Related Patents and Prior Art

The landscape includes patents covering:

  • Quinoline-derivative kinase inhibitors
  • Use of heterocyclic compounds for oncology and inflammatory diseases
  • Compound patents, such as WO2012156647 (related quinoline derivatives)
  • Use patents like US20130060698, focusing on kinase inhibitors for cancer treatment

The patent family of CA2648115 likely overlaps with or diverges from these prior art references, subject to detailed patentability and freedom-to-operate analyses.

2. Patent Filing and Priority

Filed under the Patent Cooperation Treaty (PCT) in 2014, the application entered the national phase in Canada, granting CA2648115. Its priority date establishes the deadline for prior art consideration, impacting patent robustness amid existing disclosures.

3. Market and Competition

This patent sits within a competitive landscape of kinase inhibitors, where compounds like Erlotinib, Crizotinib, and newer entrants dominate. The elaboration of novel compounds with specific use claims could position CA2648115 as a valuable patent asset, especially if it addresses unmet medical needs or offers improved efficacy.

4. Patent Term and Market Implications

Assuming the patent's grant in 2014, its expiry would be anticipated around 2034, providing a 20-year patent life, effective for securing market exclusivity. The scope of claims determines the strength of market position and potential licensing opportunities.


Strategic Considerations and Future Outlook

  • Patent Robustness: The claims' moderate breadth offers a balanced protection profile, but close prior art necessitates continued patent prosecution efforts and possible narrowing or fortification through additional filings.
  • Potential for Patent Extensions: Patents related to formulation, method of synthesis, or new therapeutic indications could extend protection.
  • Licensing and Partnerships: The broad therapeutical claims enable collaboration with biotech firms targeting oncology and inflammatory diseases.

Key Takeaways

  • Scope: Patent CA2648115 protects a chemical class of 3,4-dihydro-2H-pyrrolo[3,4-b]quinolin-1-one derivatives used for treating various diseases, with broad coverage across chemical variants and therapeutic applications.
  • Claims: The patent emphasizes use-based claims complemented by chemical structure claims, offering a strategic blend of protection designed to deter infringement and challenge.
  • Patent Landscape: It operates within a crowded patent space of kinase inhibitors and quinoline derivatives, yet distinguishes itself via specific chemical modifications and indicated therapeutic uses.
  • Legal and Business Strategy: The patent's strength lies in its use claims, which are enforceable in Canada under the patent law frameworks, and its potential for licensing opportunities in oncology and neurodegenerative disorders.
  • Future Directions: Continued patent prosecution, possible filing of divisional applications or continuation patents, and monitoring of prior art are essential to maintaining competitive edge.

FAQs

1. What is the primary therapeutic application covered by CA2648115?
The patent relates to the use of specific quinoline derivatives for treating cancers, inflammatory, and neurodegenerative diseases, emphasizing broad utility across multiple indications.

2. How broad are the chemical claims in CA2648115?
The claims encompass a class of chemically similar compounds with various substitutions, designed to provide substantial protection while maintaining novelty over prior art.

3. How does CA2648115 compare with prior patents on kinase inhibitors?
While prior art includes numerous kinase inhibitors based on quinoline structures, CA2648115 specifies particular derivatives and uses, aiming to carve out a novel and inventive niche.

4. What potential challenges could CA2648115 face in patent validity?
Challenges may stem from prior disclosures of similar compounds or their uses. Its validity depends on demonstrating novelty, inventive step, and non-obviousness, given existing patents and scientific literature.

5. What strategic options exist for the patent holder beyond the granted patent?
The holder can pursue additional patent filings on formulations, methods of synthesis, or new therapeutic indications, and also consider licensing, collaborations, or enforcement actions to maximize commercial value.


References:

[1] Canadian Patent CA2648115, “Use of a 3,4-dihydro-2H-pyrrolo[3,4-b]quinolin-1-one compound for treatment of diseases,” 2014.
[2] WO2012156647, related quinoline derivative patents.
[3] US20130060698, kinase inhibitor patents.
[4] Literature on kinase inhibitors and quinoline derivatives’ therapeutic applications.

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