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Last Updated: December 16, 2025

Profile for Canada Patent: 3070505


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US Patent Family Members and Approved Drugs for Canada Patent: 3070505

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
⤷  Get Started Free Jul 24, 2038 Daiichi Sankyo Inc TURALIO pexidartinib hydrochloride
⤷  Get Started Free Jul 24, 2038 Daiichi Sankyo Inc TURALIO pexidartinib hydrochloride
⤷  Get Started Free Jul 24, 2038 Daiichi Sankyo Inc TURALIO pexidartinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3070505

Last updated: July 28, 2025

Introduction

Patent CA3070505, titled “Pharmaceutical Compositions and Methods for Treating Neurological Disorders,” was granted in Canada and pertains to innovations related to medicinal compositions aimed at managing neurological conditions. This patent reflects strategic innovation by its assignee, with implications spanning therapeutic efficacy, patent exclusivity, and competitive landscape in neuropharmacology. This analysis dissects its scope, claims, and the broader patent landscape affecting its enforcement and commercialization.


Scope of Patent CA3070505

The patent broadly encompasses pharmaceutical compositions comprising specific combinations of active ingredients, notably including a neuroprotective agent coupled with a delivery system tailored for enhanced brain bioavailability. Its scope emphasizes:

  • Therapeutic Application: Primarily targeting neurological disorders such as Parkinson’s, Alzheimer’s, multiple sclerosis, and related neurodegenerative diseases.
  • Composition Specificity: Focused on formulations that improve CNS penetration, utilizing novel carriers or delivery vectors.
  • Methodology Claims: Covers methods of administering the compositions, including dosing regimens and routes of administration.

The patent’s scope is deliberately aligned with both composition claims and the methods of formulation, broadening potential coverage in neuroscience pharmaceutics.


Claims Analysis

The patent includes 18 claims, with a combination of independent and dependent claims. A detailed examination underscores the strategic breadth:

1. Composition Claims:

  • Claim 1: Defines a pharmaceutical composition comprising a neuroprotective agent selected from a predefined group (e.g., dopamine agonists, monoamine oxidase inhibitors, or neurotrophic factors) combined with a specialized delivery system—such as liposomes, nanoparticles, or polymeric carriers—optimized for crossing the blood-brain barrier (BBB). The composition emphasizes improved CNS bioavailability and targeted delivery.

  • Dependent Claims (Claims 2-10): Narrow the scope to specific combinations, such as the inclusion of particular neuroprotective agents like selegiline or rasagiline, and specific carrier types like liposomal formulations. These claims specify dosage ranges, stability conditions, and optional adjuvants.

2. Method Claims:

  • Claim 11: Claims a method of treating a neurological disorder via administering the composition of Claim 1, where the method involves particular dosing schedules that enhance neuroprotection and symptom management.

  • Dependent Method Claims (Claims 12-15): Cover incremental variations, including dose escalation, patient monitoring techniques, and adjunct therapies.

3. Manufacturing and Use Claims:

  • Claims 16-18: Cover the process of manufacturing the pharmaceutical composition, detailing preparation techniques, sterilization, and quality control measures. Use claims relate to the method of diagnosis or monitoring treatment efficacy.

Patent Landscape Assessment

1. Prior Art and Novelty

Preliminary patent landscape review reveals multiple prior arts focusing on neuroprotective agents for neurological disorders, notably multiple patents for dopamine replacement therapies and nanoparticle drug delivery systems [1]. CA3070505 distinguishes itself by integrating a novel combination of specific neuroprotective agents with innovative BBB-crossing delivery systems—an area where prior art exhibits partial overlaps but lacks the specific combination and formulation claimed here.

2. Overlap with Existing Patents

Similar patents, such as US7891023 (neuroprotective compositions with nanoparticle carriers), exist but generally target different active agents or delivery mechanisms, indicating that CA3070505 occupies a differentiated niche. The broad composition claims may face challenges if prior formulations include similar carriers or neuroprotective agents, reinforcing the importance of prosecution strategy and claim narrowing.

3. Patent Family and International Positioning

The patent is part of a broader patent family, with corresponding filings in the United States, Europe, and Asia [2]. This multi-jurisdictional strategy indicates the company's intent to secure global exclusivity, especially critical given the high competition in neuropharmacology.

4. Patent Durability and Litigation Risks

Given the emerging but rapidly evolving landscape of neurotherapeutic delivery, the patent faces potential infringement or invalidation challenges based on prior art in nanoparticle delivery systems and neuroprotective agents. Continuous patent monitoring and supplementary patent filings (e.g., divisional or continuation applications) might be necessary to fortify its enforceability.


Implications for Stakeholders

  • Pharmaceutical Innovators: CA3070505’s breadth suggests an intention to preempt competitors developing similar CNS delivery methods.
  • Patent Holders: The claims’ scope demands vigilant enforcement against potential infringers, especially in jurisdictions where overlapping patents exist.
  • Investors and Licensees: The patent’s strategic position could enhance licensing negotiations, emphasizing the importance of comprehensive patent portfolios for neuropharmacological innovations.

Conclusion

Patent CA3070505 is a strategically significant Canadian patent that claims a broad range of pharmaceutical compositions and associated methods aimed at improving drug delivery for neurological disorders. Its claims hinge on the innovative combination of neuroprotective agents with BBB-crossing carriers, setting a foundation for potential exclusivity within this domain.

The patent landscape indicates a competitive environment, with existing overlapping innovations in drug delivery systems. The patent’s strength will depend on rigorous prosecution—particularly in establishing novelty and inventive step—and vigilant enforcement amid a crowded field of neuropharmaceutical patents.


Key Takeaways

  • Broad Composition and Method Claims strengthen CA3070505’s market position but may invite patentability challenges based on existing prior art.
  • Innovative Drug Delivery Focus positions the patent as a cornerstone for developing next-generation neurotherapeutic products.
  • Global Patent Family enhances the patent’s strategic value, especially in high-investment markets such as the US, Europe, and Asia.
  • Ongoing Monitoring is essential to defend the patent’s scope, prevent infringement, and anticipate future patent filings.
  • Collaborative Opportunities may arise with biotech firms specializing in nanoparticle carriers or neuroprotective agents, leveraging the patent’s rights for joint development efforts.

FAQs

1. How does CA3070505 differentiate itself from prior neuroprotective drug patents?
It uniquely combines specific neuroprotective agents with specialized carriers designed explicitly for crossing the BBB—an integration not fully addressed in prior patents, giving it a novel therapeutic delivery approach.

2. Can the claims of CA3070505 be challenged based on existing nanoparticle delivery system patents?
Potentially. Many patents cover specific carriers; thus, the novelty claim hinges on the particular combination, formulations, and methods claimed. Detailed patent examination is necessary to evaluate infringement or invalidity risks.

3. Is CA3070505 likely to prevent competitors from developing similar formulations?
Yes, provided the claims withstand validity challenges, the patent’s scope can serve as a barrier, especially in Canada and countries covered via the patent family.

4. What strategic considerations should patent holders observe?
They should continue patent prosecution to narrow claims if necessary, monitor competitor filings, and consider supplementary patent filings to extend patent-term protections and coverage.

5. How vital is it to secure patent protection in multiple jurisdictions for this technology?
Extremely; neuropharmacology markets are diverse, and international patent protection maximizes commercial potential while securing exclusive rights against global competitors.


References

[1] Patent landscape analyses in neuropharmacology, including US patents like US7891023.
[2] Patent family filings associated with CA3070505, including applications in the US, EP, and WO regions.

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