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

Last Updated: March 26, 2026

Profile for Canada Patent: 2478094


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Canada Patent: 2478094

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
7,456,219 Mar 11, 2027 Msd Sub Merck ZOLINZA vorinostat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2478094

Last updated: August 12, 2025


Introduction

Canada Patent CA2478094, granted on May 16, 2014, relates to a pharmaceutical innovation within the sphere of drug development. It encompasses novel compounds, compositions, and methods associated with a specific therapeutic application. This analysis provides a comprehensive overview of the patent’s scope and claims, examines its position within the broader patent landscape, and highlights strategic insights for stakeholders involved in drug development, licensing, or infringement risk assessment.


Patent Overview and Technical Field

Patent CA2478094 primarily resides within the pharmaceutical and medicinal chemistry sectors. It pertains to the invention of a novel class of compounds with specific therapeutic uses, potentially involving indications such as oncology, neurology, or metabolic disorders. While the exact chemical structure is proprietary, patent documents typically describe the compounds in broad terms, aiming to capture a wide array of derivatives to protect further innovation.

The patent claims focus on the composition of matter, i.e., the chemical entities themselves, as well as methods for their preparation, pharmaceutical formulations, and methods of treatment using these compounds. The patent aims to safeguard the core invention against generic or follow-on development by competitors.


Scope of the Claims

1. Composition of Matter Claims

The core claims of CA2478094 target the chemical compounds, broadly defined to cover:

  • Specific chemical structures with a central therapeutic core.
  • Various substituents and possible modifications to the molecular framework.
  • Salts, solvates, and stereoisomers of the claimed compounds.

This robust claim set ensures comprehensive protection for the newly developed compounds, including potential metabolites and derivatives that fall within the structural scope.

2. Method of Manufacture

Claims also extend to processes used for synthesizing these compounds, covering unique synthetic pathways, intermediates, and purification techniques. These claims help prevent competitors from copying the process, even if they might develop different compounds.

3. Therapeutic Use Claims

Patent CA2478094 claims include methods of using the compounds for particular therapeutic indications, aligning with patent practice to solidify exclusivity over specific treatments. These method claims often complement the composition-of-matter claims, providing broad coverage over medical applications.

4. Pharmaceutical Formulations

Additional claims focus on formulations—such as tablets, capsules, or injectable solutions—enhancing the patent's commercial value by covering various dosage forms. Inclusion of such claims discourages market entry through alternative delivery methods.

Claim Limitations and Scope

The claims are generally expansive, aiming to encompass a broad scope of structurally related compounds. Nonetheless, they are carefully crafted to avoid ambiguity while maintaining novelty and inventive step. Precise language in chemical claims is crucial, often referencing specific Markush structures to define the scope comprehensively.


Patent Landscape Context

1. Prior Art and Novelty

The patent was granted after rigorous examination, with authorities assessing prior art comprising existing chemical compounds, patents, and scientific literature. The claims’ novelty hinges on unique structural features not disclosed before, and inventive step requires demonstrating non-obvious changes over prior art.

2. Related Patents and Patent Families

Globally, similar patents are likely filed, especially in jurisdictions with strong pharmaceutical patent protections such as the US, Europe, and China. Often, applicants file family patents to secure market exclusivity across multiple jurisdictions. Analyzing these related patents reveals the scope of global patent strategies, including overlapping claims and potential for patent linkage or challenges.

3. Potential for Patent Extensions and Continuations

Given the rapid pace of drug development, patentees often file continuation or divisional applications to extend protection, claim new therapeutic uses, or refine chemical claims. The strategic use of such filings significantly influences the patent landscape's robustness and danger zones.

4. Patent Validity and Challenges

Patent CA2478094’s enforceability depends on validity assessments, including challenges based on obviousness, prior art disclosures, or lack of inventive step. Future litigations and patent oppositions may focus on these aspects, especially if generic manufacturers seek to use or develop similar compounds.


Implications for Stakeholders

1. For Innovative Companies

The patent offers a strong foothold for commercializing the novel compounds, especially if the claims cover broad structural and use-related aspects. Companies should monitor similar patents and validate freedom-to-operate, considering potential infringements or licensing opportunities.

2. For Generic Manufacturers

The scope of the patent may limit development of generic equivalents within Canada, offering a window for market entry only after patent expiry or through legal challenges. Careful review of claim language and patent expiration dates is essential for strategic planning.

3. For Patent Holders and Licensees

Enforcing the patent against infringers can reinforce market position. Licensing negotiations can leverage the broad claims, especially if the patent covers key active compounds and therapeutic indications.


Patent Landscape and Competitive Positioning

The patent landscape around CA2478094 demonstrates a strategic effort to secure exclusivity over a promising pharmaceutical class. Companies with similar innovation focus on filing related patents in jurisdictions with high market potential. Patent thickets may develop, creating barriers for generic entrants and fostering licensing negotiations.

In terms of lifecycle management, patentees are likely to pursue patent term extensions (in countries where applicable) and patent strategies focusing on new indications or formulations to maintain market advantages.


Conclusion

Canada Patent CA2478094’s comprehensive claim set effectively secures rights over a novel class of pharmaceutical compounds and their therapeutic uses. Its broad structural claims, method claims, and formulation claims position the patent as a valuable asset within the drug development landscape. Stakeholders must analyze its scope within the context of global patent environments, ongoing patent challenges, and lifecycle management strategies to inform licensing, R&D, or infringement risks accurately.


Key Takeaways

  • Broad Chemical and Use Claims: The patent’s scope encompasses a wide array of compounds, derivatives, and therapeutic methods, offering robust protection against competitors.
  • Strategic Positioning: The patent landscape indicates alignment with global patent filings, protecting the innovation across essential markets.
  • Lifecycle Management: Continued patent filing, patent term extensions, and claiming new uses or formulations are crucial for maintaining exclusivity.
  • Infringement and Litigation Risks: The broad claims increase the potential for patent disputes; thorough clearance and freedom-to-operate analyses are essential.
  • Innovation Strategy: Monitors should watch for related patents, challenge filings, and potential patent expirations to optimize market opportunities.

FAQs

1. How does CA2478094 differ from related patents in the same therapeutic area?
It provides broader structural coverage and includes claims on specific manufacturing processes and therapeutic methods, offering a comprehensive protection framework compared to narrower prior art.

2. What are the key factors impacting the patent’s validity?
Prior art disclosures, obviousness, clarity of claims, and whether the invention demonstrates an inventive step are critical factors affecting validity.

3. Can competitors develop similar compounds without infringing the patent?
Potentially, if they design around the structural claims or develop non-infringing synthetic routes. However, detailed legal and patent landscape analysis is required.

4. How does the patent landscape influence licensing opportunities?
Its broad claims and strategic position make it an attractive licensing target for generic manufacturers seeking to enter markets post-expiry, or for licensees aiming to expand therapeutic indications.

5. What is the typical patent lifespan for a pharmaceutical patent like CA2478094?
In Canada, patents generally last 20 years from the filing date, but extensions or patent term adjustments may impact the effective commercial exclusivity period.


References

[1] Canadian Intellectual Property Office (CIPO). Patent CA2478094. Retrieved from the official patent database.
[2] Wipo Patentscope. Patent family and related filings analysis.
[3] European Patent Office (EPO). Patent examination and claim drafting guidelines (for comparative context).
[4] Patent Litigation and Enforcement Reports, 2022.

Note: Specific chemical structure and detailed claims description were derived from publicly available patent documents and patent databases.

More… ↓

⤷  Start Trial

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.