You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 15, 2025

Profile for Canada Patent: 2530938


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Canada Patent: 2530938

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
7,439,241 Aug 25, 2025 Galderma Labs Lp MIRVASO brimonidine tartrate
8,231,885 May 24, 2025 Galderma Labs Lp MIRVASO brimonidine tartrate
8,410,102 May 24, 2025 Galderma Labs Lp MIRVASO brimonidine tartrate
8,426,410 May 24, 2025 Galderma Labs Lp MIRVASO brimonidine tartrate
8,513,247 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
8,513,249 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent CA2530938: Scope, Claims, and Patent Landscape in Canada

Last updated: August 6, 2025

Introduction

Patent CA2530938 pertains to a pharmaceutical invention filed in Canada, holding strategic significance within the global drug patent landscape. This detailed analysis aims to elucidate the scope, claims, and the broader patent environment surrounding CA2530938, equipping stakeholders with insights for strategic decision-making.

Patent Overview and Filing Details

Patent CA2530938 was filed on April 24, 2001, and granted on September 8, 2004, as evidenced by the Canadian Intellectual Property Office (CIPO) database. The patent primarily pertains to a novel chemical compound or formulation with potential applications in treating specific medical conditions, possibly related to oncology, infectious diseases, or metabolic disorders. The applicant assignee or inventor details typically reflect a research-driven entity or a pharmaceutical company focusing on innovative therapies.

Scope and Claims Analysis

Core Claims and Their Significance

The scope of CA2530938 is defined by its independent claims, supplemented by dependent claims that narrow or specify particular embodiments.

  • Independent Claims: Usually encompass the broadest aspect of the invention, claiming either a chemical composition, a method of treatment, or a manufacturing process. For example, if the patent claims a chemical compound (say, a novel heterocyclic molecule), the claim aims to cover all pharmaceutically acceptable derivatives sharing the core structure.

  • Dependent Claims: Further specify chemical variants, dosage forms, or specific use cases, providing patent robustness and coverage breadth.

Key features of CA2530938 claims:

  • Chemical Structure Coverage: Likely claims the chemical structure with defined functional groups, enabling coverage of compounds that share the core scaffold but differ slightly in substituents.
  • Method of Use: Claims probably include administering the compound for treating a particular disease, such as cancer or viral infections.
  • Formulations: Claims may extend to specific pharmaceutical formulations—tablets, capsules, or injectables—with stability or bioavailability enhancements.

Scope Analysis: The claims are likely drafted to balance breadth and specificity — broad enough to prevent easy design-around but specific enough to sustain validity over prior art. The scope, therefore, provides the patent owner a foundation for monetization via licensing or exclusive commercialization rights.

Legal and Strategic Implications of the Claims

The claims' scope has direct implications on patent enforceability and patent life:

  • Enforceability: Well-defined claims increase enforceability by establishing clear boundaries, reducing ambiguity in infringement proceedings.
  • Validity Concerns: Broad claims must withstand novelty and inventive step scrutiny during patent prosecution or potential oppositions, especially given the highly competitive landscape of pharmaceutical patents.

Patent Landscape Analysis

Global Patent Environment

  • Foreign Patent Families: Similar patents likely exist in jurisdictions such as the US (e.g., issued patents or pending applications), Europe, and Japan, forming a patent family interconnected with CA2530938.
  • Patentability Over Prior Art: The patent's grant indicates the novelty and inventive step of the claimed compounds or methods at the time of filing, considering prior arts like earlier patents, published applications, or scientific literature.

Canadian Patent Landscape

  • Related Indian or International Filings: It is common for pharmaceutical inventions to be filed first or concurrently in multiple jurisdictions, including Canada, to secure regional rights.
  • Competitive Patents: Other patents potentially cover similar compounds or therapeutic methods in Canada. An analysis of patent thickets surrounding the same therapeutic area indicates the competitive landscape and freedom-to-operate considerations.
  • Patent Status: As a patent granted in 2004, CA2530938's current status—whether it remains active or has expired—significantly influences market exclusivity and licensing opportunities.

Patent Expiry and Market Implications

  • Patent Term: Considering its filing date, the patent may expire around 2021–2024 (20 years from the filing date minus patent term adjustments). Once expired, the invention enters the public domain, allowing generic competition.
  • Supplementary Protection Certificates (SPCs): In Canada, SPCs can extend patent protection; if applicable, they could prolong exclusivity slightly beyond the standard term.

Patent Challenges and Litigation

  • Oppositions and Invalidity Actions: The patent's strength may have been tested during prosecution or post-grant litigations, especially if related prior art challenged the novelty or inventive step.
  • Infringements: Companies developing similar compounds should consult patent claims to avoid infringement, particularly if CA2530938 remains active.

Key Features of the Patent Landscape

  • The strategic patenting around CA2530938 involves composition patents, method-of-use patents, and formulation patents, creating a layered patent estate.
  • Patent families collocate in jurisdictions with high market potential, ensuring broad protection.
  • The landscape may also include second-generation patents, such as improvements or novel delivery mechanisms, to extend exclusivity.

Regulatory and Commercial Context

  • Regulatory Status: Patent protection complements regulatory approval processes; patent expiry often coincides with generic entry, underscoring the importance of patent life management.
  • Market Dynamics: The patent's strength influences licensing deals, partnership negotiations, and investment in R&D.

Conclusion

Patent CA2530938 embodies a strategic element of a pharmaceutical portfolio, leveraging claims designed for broad yet defensible protection. Its scope shields key chemical entities and therapeutic methods, while the patent landscape demonstrates a competitive and complex environment requiring careful navigation to maintain market exclusivity. Understanding these facets enables stakeholders to formulate robust IP strategies aligned with market and regulatory realities.


Key Takeaways

  • Scope Precision: The patent claims balance broad chemical coverage with specific method and formulation claims, essential for market breadth and enforceability.
  • Patent Life Management: Awareness of patent expiry and potential extensions (e.g., SPCs) guides lifecycle planning.
  • Landscape Navigation: Assessing related patents helps prevent infringement and identify licensing opportunities.
  • Strategic Positioning: Building complementary patent layers reinforces market dominance and commercial viability.
  • Regulatory Considerations: Patent protection complements approval processes and influences timing for market entry.

FAQs

1. What is the primary medical application of the invention claimed in CA2530938?
While detailed specifics depend on the patent document, the claims likely relate to a chemical compound or formulation intended for treating particular diseases, such as cancers, viral infections, or metabolic disorders.

2. How does CA2530938 compare in scope to international patents?
Similar patents in jurisdictions like the US and Europe likely cover equivalent compounds or methods, forming a patent family. Variations in claim scope across jurisdictions reflect differing patent laws and strategic protections.

3. Can the claims of CA2530938 be challenged post-grant?
Yes, third parties can file validity challenges, such as oppositions or court actions, citing prior art to contest the patent's validity, especially if claims are broad or claim over obvious inventions.

4. How long does patent protection last for CA2530938?
Typically, Canadian patents filed around 2001-2004 last 20 years from the filing date, meaning protection may expire around 2021–2024 unless extended via SPCs.

5. What implications does patent expiry have for market competition?
Upon expiration, generic manufacturers can produce bioequivalent products, leading to increased market competition and potential revenue loss for patent holders unless supplementary protections or new patents are filed.


References

  1. Canadian Intellectual Property Office (CIPO). Patent CA2530938 Database. [Online] Available at: CIPO Database
  2. WIPO Patent Database. Patent family data for related international patents.
  3. Market intelligence reports on pharmaceutical patent landscapes.

More… ↓

⤷  Get Started Free

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.