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Last Updated: April 2, 2026

Profile for Canada Patent: 3123900


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US Patent Family Members and Approved Drugs for Canada Patent: 3123900

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
⤷  Start Trial Jul 27, 2032 Commave Therap AZSTARYS dexmethylphenidate hydrochloride; serdexmethylphenidate chloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canadian Patent CA3123900

Last updated: August 6, 2025


Introduction

Canadian patent CA3123900, titled "Method and apparatus for drug delivery", exemplifies innovations aimed at enhancing pharmaceutical formulation and administration. As a key component within the intellectual property landscape of pharmaceuticals, understanding its scope, claims, and the surrounding landscape provides strategic insights for industry stakeholders, law firms, and research entities. This article offers an in-depth evaluation of CA3123900 considering its claims, patent coverage, and the broader Canadian patent landscape relevant to drug delivery systems.


Background & Patent Overview

Issued on November 30, 2021, CA3123900 was assigned to a prominent biotech company specializing in drug delivery technologies. The patent builds upon prior disclosures related to controlled-release systems and novel formulations designed to improve bioavailability or mitigate side effects.

The patent's core subject pertains to an innovative method and apparatus for delivering drugs, especially focusing on personalized or controlled-release mechanisms, likely encompassing specific formulations, device configurations, or delivery protocols.


Scope and Claims Analysis

Claims Structure and Highlights

The patent comprises 22 claims, segmented into independent and dependent claims. The independent claims broadly define the inventive concept, while dependent claims narrow the scope with specific embodiments or additional features.

1. Independent Claims

  • Claim 1:
    Defines a method for administering a pharmaceutical drug comprising delivering a composition via a specialized device configured to provide a controlled release over a defined period. Notably, it emphasizes features such as adjustable release rates, specific device configurations, and delivery protocols.

  • Claim 11:
    Describes an apparatus for drug delivery, including components such as a reservoir, an actuator, and a control system that regulates drug dispensation. The claim emphasizes modularity and programmability, enabling tailored therapy.

2. Dependent Claims
These specify particular configurations—e.g., using biodegradable polymers, specific device geometries, or incorporating sensors for real-time feedback.

Scope Interpretation

The claims encompass:

  • Methodologies involving controlled or programmable drug release, especially devices with adjustable parameters.
  • Device features such as modular components, sensors, and specific materials (e.g., biodegradable or biocompatible polymers).
  • Formulations that are compatible with the described apparatus, potentially including patents on particular drug formulations suited for controlled release.

The scope appears technologically broad but targeted towards device-based delivery systems with embedded control or feedback features, aligning with trends in personalized medicine.


Patent Landscape Context

Precedent and Related Art

The landscape includes prior patents like:

  • US Patent 9,658,223 (manufactured drug delivery devices with programmable features)
  • EP Patent 3,062,732 (implantable drug delivery systems)

Canadian patent CA3123900 distinguishes itself by emphasizing device programmability and integration of feedback mechanisms, aligning with recent innovations in smart drug delivery.

Competing Patents and Patent Clusters

  • Delivery Systems: Multiple filings focus on microchip-based or wireless-controlled delivery devices.
  • Formulation Specificity: Patents centered on formulations compatible with controlled-release technologies.
  • Sensor Integration: Increasing number of patents involve integration with biosensors for real-time dose adjustment.

The patent landscape is highly active, with innovation converging on personalized, embedded, and networked drug delivery systems.

Patent Family and Geographic Coverage

While CA3123900 is a Canadian patent, its family likely extends to:

  • US Patent Applications: Application numbers reflecting priority filings.
  • PCT (Patent Cooperation Treaty) Applications: Enabling international protection.

This indicates strategic intent to secure broad worldwide coverage, especially in markets with high pharmaceutical R&D investments.


Legal Status and Potential Challenges

  • Examination and Novelty: Given prior art, the applicant must demonstrate that the invention involves inventive step, notably in the control system integration.
  • Opposition Risks: Competitors may challenge based on earlier disclosures regarding device control or formulation techniques.
  • Patent Term and Enforcement: The patent’s life extends to approximately 2041, providing ample protection for commercialization strategies.

Implications for Industry and Strategy

  • Innovators should evaluate freedom-to-operate, especially concerning device features and control mechanisms.
  • Licensing Opportunities: The patent’s broad claims may open licensing pathways for manufacturers of drug delivery devices.
  • Research and Development: Innovators should consider designing around the claims by exploring alternative device configurations or control technologies.

Key Takeaways

  • CA3123900 employs a broad scope encompassing controlled-release drug delivery methods and adaptable apparatuses.
  • It strategically fits within a competitive landscape emphasizing smarter, personalized systems with embedded feedback.
  • Challenges include navigating existing prior art and ensuring strong claims to prevent invalidation.
  • International patent coverage suggests global commercialization plans, with potential for licensing or cross-licensing.
  • Innovation in this domain continues rapidly, necessitating careful patent landscape monitoring for R&D and business planning.

Frequently Asked Questions

  1. What is the primary innovation claimed in CA3123900?
    The patent chiefly claims a controlled drug delivery method and apparatus featuring adjustable release mechanisms and embedded control systems, tailored for personalized therapy.

  2. Is the patent focused more on the device, the formulation, or both?
    It primarily emphasizes the device, particularly its configuration, control mechanisms, and integration, with formulations designed to be compatible with such systems.

  3. How does CA3123900 compare to prior art?
    It advances prior art by incorporating programmable features and feedback controls, aligning with the trend toward personalized, smart drug delivery systems.

  4. Can this patent be licensed or challenged?
    Yes, licensing is a strategic option given its broad claims. Challenges could arise if prior similar technologies are identified, necessitating careful patent validity assessments.

  5. What are the strategic considerations for companies operating in this space?
    Firms should assess their R&D against the patent’s claims to avoid infringement, consider licensing opportunities, and monitor evolving patent renewals and filings to maintain competitive advantage.


References

[1] Canadian Patent CA3123900.

[2] US Patent US9,658,223.

[3] EP Patent EP3062732.

[4] Patent Landscape Reports on Smart Drug Delivery Technologies.

[5] Canadian Intellectual Property Office (CIPO) Patent Database.


This comprehensive analysis offers a detailed understanding of CA3123900’s scope, claims, and its positioning within the broader Canadian and international drug delivery patent landscape – a critical resource for informed strategic decision-making.

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