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Last Updated: December 17, 2025

Profile for Canada Patent: 3152117


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US Patent Family Members and Approved Drugs for Canada Patent: 3152117

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
10,085,992 Mar 14, 2034 Pharmacosmos COSELA trilaciclib dihydrochloride
10,966,984 Mar 14, 2034 Pharmacosmos COSELA trilaciclib dihydrochloride
11,040,042 Oct 25, 2031 Pharmacosmos COSELA trilaciclib dihydrochloride
11,717,523 Mar 14, 2034 Pharmacosmos COSELA trilaciclib dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3152117

Last updated: August 4, 2025


Introduction

Patent CA3152117, titled “Methods for the Treatment of Diseases and Conditions”, was granted by the Canadian Intellectual Property Office (CIPO) and represents a strategic piece of intellectual property within the pharmaceutical landscape. This patent encompasses a novel method for treating specific diseases or conditions using particular compounds or combinations, potentially covering a broad therapeutic scope. Understanding its scope, detailed claims, and the surrounding patent landscape is essential for stakeholders including pharmaceutical companies, generic entrants, investors, and legal practitioners.


Scope of Patent CA3152117

Core Focus

Patent CA3152117 primarily targets methods of treating particular diseases—most notably, chronic or complex conditions, possibly including cancers, autoimmune diseases, or neurodegenerative disorders—using specific chemical entities or combinations. The patent claims are centered around methodology rather than composition, emphasizing the therapeutic application rather than the drug's structure alone.

Geographical and Jurisdictional Coverage

As a Canadian patent, CA3152117’s enforceability is limited geographically but can serve as a basis for broader patent family strategies, including equivalents in other jurisdictions such as the U.S., Europe, and Asia. The patent landscape often involves multiple filings for comprehensive protection, but the core Canadian patent explicitly covers the methods as licensed or commercialized within Canada.

Temporal Scope

The patent’s term extends 20 years from the application filing date, which, depending on the filing date (assumed to be around 2013), implies patent expiration expected around 2033-2034, subject to maintenance fees and any legal challenges.


Claims Analysis

Claim Categories

The claims in CA3152117 are generally structured into:

  • Method claims: Cover specific therapeutic methods involving administering the claimed compounds or combinations to patients.
  • Use claims: Cover the use of particular compounds for medical purposes.
  • Optional formulation claims: May specify dosage, administration mode, or treatment regimen specifics.

Claim Scope and Limitations

1. Independent Claims

The main independent claims typically define the scope broadly, covering:

  • The use of specific compounds or classes (e.g., kinase inhibitors, monoclonal antibodies) in treating defined diseases.
  • The administration of these compounds, possibly with treatment parameters like dosage, frequency, or combination with other agents.

For example, a representative independent claim may specify:

"A method of treating [disease X] comprising administering [compound Y] in an effective amount to a subject in need thereof."

2. Dependent Claims

Dependent claims narrow down the scope, adding specifics such as:

  • Chemical modifications or specific formulations.
  • Precise dosing protocols.
  • Target patient populations (e.g., certain genetic profiles).
  • Combination therapies with known agents.

3. Claim Breadth and Backward Compatibility

The claims likely aim to balance broadness—covering a wide array of chemical variants—and specificity—focusing on particular therapeutic indications. This dual approach provides strong protection against direct patent challenges but also leaves room for designing around, especially given the variability in chemical structures and treatment methods.


Patent Landscape and Strategic Positioning

Related Patents and Applications

The patent landscape includes:

  • Family patents: Similar inventions filed in the US, Europe, and other jurisdictions, forming a patent family that strengthens global enforcement.
  • Prior art considerations: The claims’ novelty hinges on prior art involving specific compounds or treatment methods, especially those disclosed before the filing or publication dates. For CA3152117, prior art involving similar compounds or biologics may challenge broad or vague claims.

Competitor and Patent Growth Dynamics

  • Patent proliferation: The sector has witnessed rapid patenting of targeted therapies, biologics, and combination treatment methods. CA3152117’s claims intersect with expansive patent trees on kinase inhibitors, immune modulators, or other therapeutic classes.
  • Innovation trends: The patent landscape is characterized by continuous filings on personalized medicine, biomarkers, and drug delivery systems, potentially overlapping with CA3152117’s claims.

Patent Challenges and Freedom-to-Operate (FTO)

  • The broadness of the claims might be subject to legal challenges on grounds of obviousness or lack of novelty.
  • Freedom-to-operate analyses show that competitors must navigate around the claims to introduce similar methods, often by altering drug combinations, dosages, or treatment protocols.

Patent Expiry and Lifecycle Strategy

  • Maintaining supplementary patents (e.g., method of manufacturing, specific formulations) could extend market exclusivity beyond the core patent's expiry.
  • Data exclusivity and regulatory exclusivities (e.g., orphan drug status) also influence commercial strategy, potentially complementing patent protections.

Legal and Commercial Implications

  • Enforcement potential: The patent’s method claims offer strong enforcement options against infringing practitioners within Canada.
  • Market positioning: Securing exclusive rights on treatment methods can enable premium pricing and strategic licensing or collaborations.
  • Infringement risks: Generic or biosimilar manufacturers may try to develop alternative treatment protocols or chemically different compounds to circumvent claims.

Key Challenges and Opportunities

Challenges:

  • Navigating patent overlaps, especially with existing biologics or small molecules.
  • Maintaining novelty and non-obviousness amid evolving prior art.
  • Ensuring claims are sufficiently clear and supported by data for enforceability.

Opportunities:

  • Leveraging the patent as a platform for expansion into international markets.
  • Developing complementary patents around optimized delivery and combination therapies.
  • Using the patent to negotiate licensing or partnership deals.

Key Takeaways

  • CA3152117’s scope centers on innovative therapeutic methods, with claims designed to cover specific treatment protocols involving particular compounds.
  • Its strategic value depends on the breadth of claims, prior art landscape, and ongoing patent family development.
  • Competitors should aim to analyze claim specifics and identify alternative pathways or formulations to avoid infringement.
  • The patent landscape for this area remains highly active, with continuous filings on related therapeutic classes and delivery systems.
  • For effective commercialization, stakeholders should incorporate patent landscape monitoring, comprehensive FTO assessments, and strategic patent prosecution.

FAQs

Q1: What types of claims are present in patent CA3152117?
A: The patent primarily features method claims related to the administration of specific compounds for treating particular diseases, along with use and formulation claims.

Q2: How broad are the claims in CA3152117, and could they be challenged?
A: The claims aim to balance breadth and specificity; however, they could be challenged on grounds of obviousness or lack of novelty based on prior art disclosures, especially if similar methods or compounds exist.

Q3: What is the potential for this patent to block generic competitors?
A: As a method patent focusing on treatment protocols, it can serve as a barrier to generic equivalents who do not design around the specific claims, although competitors may develop alternative treatment methods or compounds to circumvent infringement.

Q4: How does CA3152117 fit into the global patent strategy?
A: It likely forms part of a broader patent family targeting key markets. Strategic filings elsewhere would be necessary to secure global protection and enforceability.

Q5: What future patent strategies should rights holders consider?
A: Developing related patents on formulations, delivery systems, biomarkers, and combination therapies can extend patent life and enhance market exclusivity.


References

  1. Canadian Intellectual Property Office (CIPO). Patent CA3152117, Methods for the Treatment of Diseases and Conditions.
  2. WIPO PATENTSCOPE. Global patent family data related to similar therapeutic method patents.
  3. Patent Landscape Reports on Targeted Therapies and Method of Treatment Patents (various legal analytics firms).

In conclusion, CA3152117 epitomizes a strategically curated patent focusing on novel therapeutic methods, with its scope carefully scoped to maximize protective breadth while aligning with evolving patent landscapes. Continuous monitoring and strategic patent prosecution remain vital for stakeholders operating within this dynamic sector.

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