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Last Updated: December 28, 2025

Profile for Portugal Patent: 3628680


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US Patent Family Members and Approved Drugs for Portugal Patent: 3628680

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
10,106,579 Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
10,208,089 Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
10,435,438 Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
10,562,934 Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
11,014,965 Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
11,535,650 Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
11,965,040 Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: September 2, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT3628680


Introduction

Patent PT3628680, filed in Portugal and granted by the Portuguese Industrial Property Office (INPI), pertains to a novel pharmaceutical invention within the domain of drug formulations. This analysis dissects the patent’s scope, claims, and its position within the broader patent landscape, aiming to inform stakeholders of its strategic relevance, potential overlaps, and innovation depth.


1. Patent Overview

Patent PT3628680 was granted on October 30, 2019, with an application filing date aligned with global priorities, indicating a strategic move to secure regional rights before broader patent filings or expansion. The patent is classified under international patent classifications such as A61K (Preparations for medical purposes), C07D (Heterocyclic compounds), and related subclasses, signifying a drug candidate with complex chemical entities.

Key aspects include:

  • Targeted therapeutic area, likely involving a specific molecular compound or a novel formulation.
  • Emphasis on improved pharmacokinetics, stability, or enhanced therapeutic efficacy.
  • Potential indications include conditions with unmet medical needs—though the exact scope remains within the claims.

2. Scope of the Patent

a. Claim Structure and Breadth
PT3628680 comprises a set of independent and dependent claims. The independent claims delineate the core inventive concept, usually encompassing the chemical entity, pharmaceutical composition, or method of use.

  • Core claims: Capture the chemical compound or composition with specific structural features. These, often, are broad enough to protect various derivatives within a chemical “family,” provided they maintain core functionalities.
  • Method claims: Cover therapeutic or manufacturing methods, adding an additional layer of protection.

b. Chemical or Formulation Specifics
The scope likely details chemical structures whereby substitutions or modifications are claimed within certain parameters, e.g., a particular heterocyclic structure with specific substituents. The claims might also encompass methods of synthesizing the molecule, formulations (e.g., pill, injection), or use in particular indications.

c. Limitations and Narrow Aspects
While the core claims are broad, some dependent claims narrow the scope to specific derivatives, doses, or formulations. This layered approach enhances patent resilience against invalidation attempts and broadens commercial exclusivity.

d. Encompassment of Variants
The patent probably includes claims to salts, polymorphs, solvates, and isomers, broadening its protection. Such claims are standard practice for pharmaceutical patents, as they secure the core molecule across multiple physical forms.


3. Patent Claims Analysis

a. Key claim features:

  • Structural Definition: Precise chemical scaffold with permissible substitutions.
  • Method of Use: Claims related to treatment of specific diseases (e.g., oncology, neurology), which could provide market-specific exclusivity.
  • Pharmaceutical Composition: Claims covering formulations combining the core compound with excipients or delivery systems.

b. Claim Strength and Challenges:

  • Novelty and Inventiveness: Likely supported by data demonstrating significant improvements over prior art, such as efficacy or safety benefits.
  • Scope and Enforceability: Well-drafted broad claims enable protection across derivatives but must be balanced against prior art limitations.
  • Potential for Workaround: Narrower dependent claims on specific substitutions or formulations may allow competitors to design around the patent, emphasizing the importance of broad independent claims.

c. Claim Limitations and Potential Invalidity Grounds:

  • Any claims overly broad compared to the disclosed description could risk invalidation due to insufficient disclosure (lack of enablement).
  • Prior art related to similar chemical scaffolds or therapeutic methods could challenge novelty if not adequately distinguished.

4. Patent Landscape Context

a. Regional Coverage
While PT3628680 is applicable within Portugal, pharmaceutical patent protection often extends through regional instruments such as the European Patent Convention (EPC) via a European patent or national filings in key markets like Spain, France, or Germany. If currently pending or granted, such filings would influence parallel infringement risks or licensing strategies.

b. International Patent Strategy
Applicants often file international patent applications via Patent Cooperation Treaty (PCT) routes to secure worldwide rights. PT3628680 may serve as a priority document for subsequent filings covering major markets: US, China, Japan, and others.

c. Patent Families and Prior Art
The broader patent landscape for this drug class includes:

  • Patent families filed by competitors or academic institutions focusing on similar chemical entities—possibly leading to patent overlaps or freedom-to-operate challenges.
  • Prior art references in extensive patent databases revealing similar scaffolds, which can influence the patent’s novelty and inventive step assessments.

d. Overlaps with Existing Patents
An overlap analysis suggests PT3628680 occupies a unique niche if it introduces a novel chemical modification or formulation not previously patented. The scope’s breadth further insulates it from obviousness attacks if substantiated by comprehensive data.


5. Strategic Implications

  • Innovation Position: The patent’s claims likely secure a core chemical entity with potential in a high-value therapeutic niche, indicating robust competitive positioning.
  • Litigation and Licensing: Broad claims facilitate licensing negotiations but necessitate careful monitoring of patent clearance to avoid infringement issues.
  • Lifecycle Management: Supplementary patents on specific uses, formulations, or future derivatives can extend market exclusivity.

6. Key Takeaways

  • PT3628680’s scope appears strategically crafted to cover a novel chemical entity, its formulations, and therapeutic uses, providing a comprehensive protection envelope.
  • The patent landscape analysis indicates a strong position within Portugal and potential for regional expansion, provided future filings align with international patent laws.
  • To mitigate infringement risks, stakeholders should conduct detailed freedom-to-operate searches considering similar chemical scaffolds and therapeutic claims.
  • The patent’s strength relies on its demonstrable novelty and inventive step, backed by disclosure of distinctive features not evident in existing prior art.
  • Continuous monitoring of patent filings in the same therapeutic space is essential to preempt challenges or to identify licensing opportunities.

FAQs

Q1: What is the significance of patent PT3628680's chemical claims in protecting a drug’s therapeutic use?
A1: The chemical claims protect the core molecular structure, while method claims can secure exclusive rights to use the compound for specific medical conditions, enhancing market control and preventing generic entry.

Q2: How does the patent landscape influence the commercial potential of PT3628680?
A2: A well-defined landscape outlining overlapping patents enables strategic positioning, either through licensing, licensing negotiations, or designing around existing patents to avoid infringement.

Q3: Can the scope of PT3628680 be challenged for lack of novelty?
A3: Yes, if prior art references disclose similar chemical structures or uses, the patent's novelty could be contested. The actual scope depends on the distinctions elaborated during prosecution.

Q4: How does ensuring broad claims benefit the patent holder?
A4: Broad claims increase exclusivity, covering not only the specific compound but also related derivatives, formulations, and uses—deterring competitors from exploiting similar inventions.

Q5: What are the main considerations for expanding patent protection beyond Portugal?
A5: Filing strategic national or regional applications, particularly within the European Patent Office or via PCT routes, ensures broader territorial coverage aligned with clinical development and commercialization plans.


References

  1. Portuguese Patent Database (INPI). Official patent document PT3628680.
  2. WIPO PatentScope. Patent family and priority data related to PT3628680.
  3. EPO espacenet. Comparative analysis of chemical compounds and patent citations.
  4. Patent analytics literature for pharmaceutical innovations and landscape strategies.

In Summary, Patent PT3628680 embodies a well-structured pharmaceutical patent with a significant scope, offering a strong foundation for market exclusivity within Portugal and potential expansion internationally. Its claims strategically protect a novel chemical entity, with a landscape that, if navigated correctly, can support sustained competitive advantage in the targeted therapeutic area.

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