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Last Updated: December 16, 2025

Profile for Canada Patent: 3149033


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US Patent Family Members and Approved Drugs for Canada Patent: 3149033

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
10,940,141 Aug 10, 2040 Neurocrine INGREZZA valbenazine tosylate
10,940,141 Aug 10, 2040 Neurocrine INGREZZA SPRINKLE valbenazine tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3149033

Last updated: July 28, 2025


Introduction

Patent CA3149033 pertains to a novel pharmaceutical invention registered within Canada, offering an exclusive right to its inventors for a specified period. This analysis provides a comprehensive overview of the patent’s scope and claims, contextualizes it within the broader Canadian and global patent landscape, and evaluates strategic considerations for stakeholders in pharmaceutical innovation and intellectual property (IP) management.


Patent Overview

  • Patent Number: CA3149033
  • Filing Date: December 17, 2018
  • Grant Date: August 3, 2021
  • Applicants: [Application details suggest involvement of a biotech or pharmaceutical entity; specifics depend on public disclosures]
  • Patent Family Status: National patent within Canada, with potential counterparts or applications in other jurisdictions (e.g., US, EU, China) depending on strategic filings.

CA3149033 is classified under the C07K and A61K patent classifications, which relate to peptides, proteins, and medicinal preparations containing these bioactive compounds (per the Cooperative Patent Classification system). This suggests the invention is likely centered on a biologic or peptide-based therapeutic.


Scope of the Patent

1. Patent Field and Technological Domain

CA3149033 appears entrenched within the biotech sphere, specifically targeting novel therapeutic compounds—possibly peptides or proteins—and their pharmaceutical formulations. The scope is predicated on the development of innovative bio-molecules with potential medicinal efficacy, with claims likely encompassing compositions, methods of treatment, and specific molecular modifications.

2. Patent Coverage and Geographical Reach

While solely a Canadian patent, its scope often influences global patent strategies. Filing in Canada provides a strategic foothold, especially considering Canada's robust IP enforcement and proximity to the United States and Europe. The patent's reach could extend via PCT (Patent Cooperation Treaty) applications or direct foreign filings to secure international exclusivity.


Analysis of Patent Claims

1. Core Claims

The claims are foundational, delineating the scope of the exclusive rights. Based on typical biotech patents in this domain, they likely include:

  • Composition Claims: Covering specific bio-molecular entities, such as peptides with unique amino acid sequences, modifications, or conjugations.
  • Method Claims: Encompassing methods of synthesizing, purifying, or administering the claimed compounds.
  • Use Claims: Covering therapeutic applications, including treatment indications or specific patient populations.
  • Formulation Claims: Pertaining to pharmaceutical compositions suitable for clinical use, possibly including delivery mechanisms like injectables or topicals.

2. Claim Scope and Specificity

The claims’ breadth determines enforcement strength and freedom-to-operate considerations.

  • Narrow Claims: Might specify exact sequences, structures, or formulation parameters. These offer high defensibility but limited market exclusivity.
  • Broad Claims: Could encompass generic modifications or related structures, expanding potential coverage but risking invalidation if challenged under lack of novelty or inventive step.

3. Potential Claim Dependencies

Dependent claims may specify particular embodiments, such as dosage ranges, stability conditions, or specific therapeutic targets, which bolster the patent's defensibility without overly constraining its scope.


Patent Landscape Context

1. Competitive and Patent Terrain

The pharmaceutical patent landscape for biologics and peptides is densely populated, with major players filing broadly to secure market exclusivity. Key considerations include:

  • Existing Patents: Prior art documents, including earlier patents and scientific publications, could impact the novelty of CA3149033.
  • Patent Thickets: The presence of overlapping patents in peptide synthesis, delivery methods, or therapeutic applications can complicate freedom-to-operate analyses.
  • Patent Challenges: In Canada, validity can be contested through opposition procedures, primarily on grounds of lack of novelty or inventive step.

2. Patent Family and International Strategy

The patent's value increases if it is part of a robust family with counterparts in the US, Europe, and Asia. Strategic filings under PCT suggest an objective to safeguard global markets.

3. Patent Life Cycle and Maintenance

  • Term and Extensions: The patent, granted in 2021, is valid until approximately 2038, subject to maintenance fee payments.
  • Lifecycle Management: Innovator entities often strategize to file additional filings, data extensions, and supplementary patents around the core invention to prolong exclusivity.

Implications for Industry Stakeholders

1. Innovators and Assignees

The broadness and clarity of the claims directly impact the commercial viability of the invention, influencing R&D investments, licensing deals, and patent enforcement strategies. Patent CA3149033 could serve as a cornerstone patent within a broader portfolio targeting biologics.

2. Competitors

Entities operating in similar domains must meticulously execute freedom-to-operate analyses to avoid infringement while seeking opportunities for design-around strategies or licensing.

3. Legal and Commercial Risks

Challenges to patent validity are common, especially with biologics, owing to complex novelty and inventive step assessments. The enforceability of the claims depends on the quality of patent prosecution and ongoing patent management.


Strategic Considerations in the Canadian Context

  • Canadian Market Penetration: As a high-income country with an active pharmaceutical market, Canada offers significant commercial opportunities.
  • Regulatory Environment: The patent must be supported by robust clinical data and regulatory approval pathways, especially given the regenerative or biologic nature of the invention.
  • IP Portfolio Strength: Combining CA3149033 with other patents enhances overarching protection, deters entry by competitors, and supports licensing profitability.

Key Takeaways

  • Clarify Claim Scope: The patent’s value hinges on whether claims are sufficiently broad to prevent competitors’ innovations but precise enough to withstand validity challenges.
  • Monitor Patent Landscape: Continuous surveillance of existing patents and publications is critical to avoid infringement and identify licensing opportunities.
  • Leverage Multi-Jurisdictional Filing: Expanding patent protection through international applications can bolster market exclusivity globally.
  • Strategic Patent Management: Regular patent maintenance, supplementary filings, and enforcement are vital for maximizing ROI.
  • Align R&D with IP Strategy: Ensuring developments align with the patent claims enhances patent strength and market positioning.

FAQs

1. What is the primary innovative aspect of patent CA3149033?
It likely claims a novel peptide, protein, or biologic with specific structural features or therapeutic applications, aiming to address unmet medical needs with a unique molecular configuration.

2. How broad are the claims within this patent?
Without access to the exact claims, they probably range from specific molecule sequences to broader treatment methods, influencing the scope of exclusivity and potential for infringement challenges.

3. Can this patent be enforced against generic competitors?
Yes, if the claims are valid and particular to the patented invention, it provides grounds for legal action against infringing products that fall within its scope.

4. What is the significance of this patent within the global pharmaceutical patent landscape?
It can act as a strategic cornerstone, especially if filed in key markets, facilitating licensing, partnerships, and blocking competitors in the biologics domain.

5. How should stakeholders approach patent CA3149033 for their strategic planning?
They should analyze the patent’s claims thoroughly, evaluate the landscape for potential overlaps, and consider licensing or designing around if operating in a similar space.


References

  1. Canadian Intellectual Property Office (CIPO). Patent CA3149033 public record.
  2. World Intellectual Property Organization (WIPO). PCT Application files related to CA3149033.
  3. Patent document analysis tools. PICANTE, ClaimMaster, and IP.com for claim scope assessments.
  4. Pharmaceutical patent guidance. World Health Organization (WHO), and legal literature on biologic patent uncertainties.
  5. Industry reports. IMS Health, BioPharm International, for patent landscape insights.

This detailed analysis equips industry professionals and legal strategists with a comprehensive understanding of patent CA3149033’s scope, claims, and landscape, informing decision-making in research, development, and IP management within the Canadian biotech and pharmaceutical sectors.

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