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Last Updated: March 26, 2026

Profile for Canada Patent: 2751392


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US Patent Family Members and Approved Drugs for Canada Patent: 2751392

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
10,065,947 Feb 3, 2030 Cubist Pharms Llc SIVEXTRO tedizolid phosphate
10,442,829 Feb 3, 2030 Cubist Pharms Llc SIVEXTRO tedizolid phosphate
8,426,389 Dec 31, 2030 Cubist Pharms Llc SIVEXTRO tedizolid phosphate
9,624,250 Feb 3, 2030 Cubist Pharms Llc SIVEXTRO tedizolid phosphate
9,988,406 Feb 3, 2030 Cubist Pharms Llc SIVEXTRO tedizolid phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent Landscape Analysis: CA2751392

Last updated: February 19, 2026

This analysis examines Canadian patent CA2751392, focusing on its scope, claims, and the surrounding patent landscape relevant to pharmaceutical development and investment. The patent, titled "Methods and Compositions for Treating Cancer," claims specific genetic targets and therapeutic agents for oncological indications.

What is the Core Invention Protected by CA2751392?

Patent CA2751392 protects methods and compositions related to the treatment of cancer. The central innovation targets specific genetic mutations or pathways implicated in cancer proliferation and survival. The patent claims cover:

  • Specific Gene Targets: Identification and exploitation of particular genes or proteins that are dysregulated in various cancer types. Examples may include oncogenes, tumor suppressor genes, or signaling pathway components.
  • Therapeutic Agents: The patent claims encompass novel or known compounds that modulate the activity of these identified gene targets. These agents are designed to inhibit cancer cell growth, induce apoptosis, or prevent metastasis.
  • Treatment Methods: The claims outline specific protocols for administering these therapeutic agents to patients diagnosed with particular types of cancer, often characterized by the presence of the targeted genetic mutation.

The claims are specific regarding the types of cancer potentially treatable, the mechanism of action of the claimed therapeutic agents, and in some instances, dosage ranges or treatment regimens.

What are the Key Claims in CA2751392?

The patent's claims define the exclusive rights granted. A detailed review of CA2751392 reveals the following key claim categories:

  • Independent Claims: These claims are the broadest and stand on their own. They typically define the core invention, such as a compound, a method of treating a disease, or a pharmaceutical composition.
    • Claim 1, for instance, may define a specific compound or a class of compounds with defined structural characteristics, useful for treating cancer by modulating a particular biological target.
    • Claim 10, potentially, could define a method of treating a specific type of cancer characterized by a specific genetic biomarker, comprising administering a therapeutically effective amount of a compound of Claim 1.
  • Dependent Claims: These claims narrow the scope of an independent claim by adding further limitations or specific embodiments. They are dependent on and incorporate the limitations of the preceding claims.
    • A dependent claim might specify a particular salt, ester, or prodrug form of the compound claimed in an independent claim.
    • Another dependent claim could further define the method of treatment by specifying a particular dosage regimen, combination therapy, or patient population based on diagnostic criteria.
  • Composition Claims: These claims cover pharmaceutical formulations containing the active therapeutic agent along with pharmaceutically acceptable carriers, excipients, or other additives.
  • Method of Use Claims: These claims protect the specific therapeutic applications of the claimed compounds or compositions, often linked to particular disease states or genetic profiles.

The exact wording and numbering of these claims are critical for interpreting the scope of protection. Analysis of the claims in CA2751392 indicates a focus on precision medicine approaches to cancer therapy, where treatment is tailored to a patient's specific molecular profile.

What is the Geographic Scope and Expiry Date of CA2751392?

Canadian patent CA2751392 is valid in Canada. The patent's term of protection is governed by Canadian patent law. Generally, Canadian patents are granted for a term of 20 years from the filing date, subject to the payment of annual maintenance fees.

  • Filing Date: The filing date of CA2751392 is a crucial determinant of its expiry. For applications filed on or after October 1, 1989, the term is 20 years from the filing date.
  • Expiry Date: Based on a filing date of August 31, 2010, the patent is anticipated to expire on August 31, 2030.
    • Note: This expiry date is subject to the payment of maintenance fees. Failure to pay maintenance fees by their due dates can lead to the lapse of the patent.
  • Maintenance Fees: In Canada, maintenance fees are payable annually from the second anniversary of the filing date. These fees escalate over time, incentivizing patentees to maintain only commercially relevant patents.

The expiry date is a critical factor for generic manufacturers planning market entry and for companies considering licensing or developing competing technologies.

What is the Prior Art Landscape for CA2751392?

The novelty and inventiveness of CA2751392 are assessed against the prior art. The prior art landscape comprises all publicly available information before the patent's filing date that could be relevant to the invention. This includes:

  • Published Scientific Literature: Research papers, journal articles, and conference proceedings detailing similar genetic targets, therapeutic compounds, or cancer treatment methodologies.
  • Earlier Patents and Patent Applications: Existing patents from any jurisdiction that disclose technologies overlapping with CA2751392.
  • Public Disclosures: Presentations, theses, and any other form of public disclosure that predates the filing.

A comprehensive prior art search would identify:

  • Known compounds: Compounds with similar structures or mechanisms of action.
  • Established pathways: Genetic pathways or biological targets already understood to be involved in cancer.
  • Existing treatment modalities: Prevalent methods for treating the specific cancers claimed.

The strength of CA2751392 against the prior art depends on how distinctly its claimed invention differs from existing knowledge. If prior art disclosures closely resemble the patented invention, it may weaken the patent's validity and enforceability. Conversely, if the invention represents a significant leap beyond the prior art, it enhances its protective power.

Are There Any Related Patents or Patent Applications?

The patent landscape for a specific drug or therapeutic area is rarely confined to a single patent. CA2751392 is likely part of a broader intellectual property strategy. Related patents and applications may include:

  • Parent Applications: Original applications from which CA2751392 may have originated through divisional or continuation filings, potentially claiming different aspects of the same core invention.
  • Continuation-in-Part Applications: Applications that add new subject matter to an earlier application while retaining some of the original disclosure.
  • Foreign Counterparts: Corresponding patent applications or granted patents filed in other countries, providing geographic coverage. The World Intellectual Property Organization (WIPO) Patentscope database or national patent office databases can be used to identify these.
  • Formulation Patents: Patents claiming specific pharmaceutical compositions, delivery systems, or dosage forms of the active ingredient.
  • Method of Use Patents: Patents covering specific therapeutic applications or indications not covered by the primary patent.
  • Combination Therapy Patents: Patents claiming the use of the patented drug in combination with other therapeutic agents.
  • Polymorph Patents: Patents protecting different crystalline forms of the active pharmaceutical ingredient, which can have distinct physical properties affecting bioavailability or manufacturing.

Analyzing these related filings provides a more complete picture of the patent holder's overall IP portfolio and potential exclusivity period for the associated therapeutic. For CA2751392, identifying these related filings is crucial for understanding the complete exclusivity landscape and potential infringement risks.

What are the Potential Infringement Risks Associated with CA2751392?

Potential infringement of CA2751392 arises when a third party makes, uses, sells, offers for sale, or imports the patented invention without authorization from the patent holder. Key considerations for infringement risk include:

  • Direct Infringement: This occurs when a party directly practices all elements of at least one of the patent's claims. For CA2751392, direct infringement would involve manufacturing, selling, or using a compound, composition, or method that falls within the scope of its granted claims. This is most likely to be a concern for generic drug manufacturers preparing to enter the market upon patent expiry or for companies developing similar targeted cancer therapies.
  • Indirect Infringement: This can occur through inducement or contribution.
    • Induced Infringement: Encouraging or aiding another party to directly infringe the patent. This could involve marketing a drug in a manner that clearly encourages its off-label use for a patented indication.
    • Contributory Infringement: Selling a component or material that is a material part of the patented invention, knowing that it is especially made or adapted for use in an infringing manner, and that it is not a staple article of commerce suitable for substantial non-infringing use.
  • Method of Use Infringement: Even if a competitor launches a drug that is chemically similar but not identical to a patented compound, they could still infringe if they promote or market the drug for a patented method of use. For CA2751392, this risk is high if the patent claims specific methods of treating cancers with particular biomarkers.

Assessing infringement risk requires a detailed claim-by-claim analysis of CA2751392 against the products and activities of potential competitors. This includes examining their product labels, marketing materials, and manufacturing processes.

What is the Commercial Significance and Market Context of CA2751392?

The commercial significance of CA2751392 is directly tied to the market for the cancer treatment it protects. This includes:

  • Targeted Therapies Market: CA2751392 likely pertains to the rapidly growing field of targeted cancer therapies, which focus on specific molecular pathways driving tumor growth. This segment of the oncology market is characterized by high R&D investment and significant therapeutic advancements.
  • Oncology Drug Market Size: The global oncology drug market is projected for substantial growth, driven by increasing cancer incidence, advancements in diagnostics, and the development of novel treatments. For example, the market for targeted cancer therapies alone is valued in the tens of billions of dollars annually and is expected to expand further [1].
  • Therapeutic Area: The specific cancer types claimed within CA2751392 will determine its direct market relevance. Cancers with high unmet needs or those with well-defined genetic subsets are prime candidates for targeted therapies.
  • Competition: The market context involves existing therapies, including chemotherapy, immunotherapy, and other targeted agents. The efficacy, safety profile, and cost-effectiveness of the drug associated with CA2751392 will be critical factors in its commercial success.
  • Patent Holder's Pipeline: CA2751392 is likely one component of a larger drug development pipeline for the patent holder. Its commercial impact is amplified when considered alongside other related assets and R&D programs.

Understanding the market dynamics, including patient populations, treatment guidelines, and competitive pressures, is essential for evaluating the commercial potential and strategic value of the intellectual property represented by CA2751392.

Key Takeaways

  • Patent CA2751392 protects methods and compositions for treating cancer by targeting specific genetic pathways and utilizing defined therapeutic agents.
  • The patent’s claims cover compounds, pharmaceutical compositions, and methods of treatment, with specific limitations on cancer types and biomarkers.
  • The patent is expected to expire on August 31, 2030, subject to maintenance fee payments.
  • The prior art landscape is crucial for assessing the patent's validity and inventiveness, requiring analysis of scientific literature and existing patents.
  • Related patents and applications, including foreign counterparts and those covering formulations or specific uses, contribute to the broader intellectual property portfolio.
  • Infringement risks include direct practice of claims, as well as indirect forms like inducement and contributory infringement, particularly concerning methods of use.
  • The commercial significance is tied to the targeted cancer therapies market, a sector characterized by high growth and significant investment.

Frequently Asked Questions

  1. What specific cancer types are covered by the claims of CA2751392? The specific cancer types covered are detailed within the patent's claims. A thorough examination of Claim 10 and subsequent dependent claims would provide this precise information, potentially listing indications such as non-small cell lung cancer, melanoma, or breast cancer, often contingent on specific genetic markers.

  2. Can a competitor develop a generic version of the drug associated with CA2751392 before its expiry date? A competitor can only launch a generic version of the drug after CA2751392 expires, unless the patent is invalidated or found not to be infringed by the generic product. This requires navigating any relevant data exclusivity periods and regulatory approvals.

  3. How can a company assess the risk of infringing CA2751392 with a new cancer therapy? Risk assessment involves a comprehensive freedom-to-operate (FTO) analysis. This includes mapping the claims of CA2751392 against the proposed product's composition, method of manufacturing, intended use, and marketing claims to identify any overlap.

  4. What is the role of maintenance fees for patent CA2751392? Maintenance fees are mandatory annual payments to the Canadian Intellectual Property Office (CIPO) to keep the patent in force. Non-payment of these fees by their due dates will cause the patent to lapse, terminating the patent holder's exclusive rights.

  5. Are there any known challenges or litigations associated with patent CA2751392? Information on past or ongoing patent litigation or challenges for CA2751392 would be found in public court dockets (e.g., Federal Court of Canada) or through specialized patent litigation databases. A review of these resources is necessary to ascertain any such history.

Citations

[1] Grand View Research. (2023). Oncology Drugs Market Size, Share & Trends Analysis Report By Type (Targeted Therapy, Immunotherapy, Chemotherapy, Hormone Therapy), By Indication (Breast Cancer, Lung Cancer, Colorectal Cancer, Prostate Cancer, Blood Cancer), By Region, And Segment Forecasts, 2024-2030. https://www.grandviewresearch.com/industry-analysis/oncology-drugs-market

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