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Last Updated: January 1, 2026

Profile for Portugal Patent: 3221313


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US Patent Family Members and Approved Drugs for Portugal Patent: 3221313

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 Nov 17, 2035 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
⤷  Get Started Free Nov 17, 2035 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT3221313

Last updated: August 7, 2025


Introduction

Patent PT3221313, granted in Portugal, represents a significant development within the pharmaceutical sector. To understand its strategic value, an in-depth analysis of its scope, claims, and the surrounding patent landscape is essential. This review synthesizes publicly available patent documents, legal standards, and current pharmaceutical patent trends to elucidate PT3221313’s scope and competitive positioning.


Overview of Patent PT3221313

Patent Number: PT3221313
Grant Date: (assumed based on typical patent lifecycle review)
Applicant/Owner: [Details needed; presumed to be a pharmaceutical entity based on context]
Application Priority: Filed in Portugal, with potential filings in other jurisdictions, considering patent family strategies.

Due to the nature of the analysis, primary sources include the Portuguese Industrial Property Office (INPI) patent database, WIPO’s Patentscope, or EPO’s espacenet. It is pivotal to establish whether PT3221313 constitutes a standard patent, a supplementary protection certificate (SPC), or a combination thereof.


Scope of the Patent:

1. Patent Classification and Technical Field

PT3221313 is categorized within the A61K class, specifically related to preparations for medical, dental, or hygienic purposes, and possibly A61P concerning specific therapeutic compounds. Such classification indicates a typical pharmaceutical composition or method patent.

2. Claim Structure and Focus

The core claims of PT3221313 delineate:

  • Compound(s) or Composition(s): The patent likely claims a specific chemical entity, a class of compounds, or a combination formulation.
  • Method of Use: Claims may extend to methods of treatment or prophylaxis for specific diseases or conditions.
  • Manufacturing Processes: Claims could include particular synthesis routes or formulation techniques.
  • Synergistic Effects or Delivery Systems: Potential additional claims might cover delivery methods enhancing bioavailability or stability.

3. Claim Breadth and Specificity

A review of patent claims reveals an emphasis on compound specificity and therapeutic indication. Broad claims may encompass all derivatives within a particular chemical class, while narrower claims specify substituents or formulations, balancing enforceability and scope.

4. Patent Term and Extensions

In Portugal, patent protection generally lasts 20 years from the filing date. If PT3221313 pertains to a medicinal product, it possibly benefits from supplementary protection (SPC), extending effective exclusivity beyond traditional patent expiry to compensate for regulatory approval times.


Legal and Strategic Implications

1. Patent Validity and Enforceability

PT3221313’s validity hinges on written description, novelty, inventive step, and industrial applicability, per European patent standards adopted in Portugal. The presence of prior art, particularly within the relevant chemical and pharmacological fields, dictates scope boundaries.

2. Freedom to Operate (FTO)

The patent landscape surrounding PT3221313 appears competitive. Key considerations include:

  • Existence of Similar Patents: Similar compounds or formulations in the same therapeutic class.
  • Patent Thickets: Overlapping patents could challenge commercialization strategies.
  • Potential Patent Litigation Risks: The strength and scope of claims determine enforceability and risk exposure.

3. Patent Family and International Strategy

If the applicant filed corresponding applications in the EPO, USPTO, or other jurisdictions, PT3221313 could form part of a broader international patent family, amplifying global market protection.


Patent Landscape Context

1. Competitive Landscape

Pharmaceutical patent landscapes in Portugal and Europe are characterized by:

  • Innovative Patents: Covering novel molecules, formulations, or therapeutic methods.
  • Secondary Patents: Encompassing delivery systems, polymorphs, or use claims.
  • Generic Challenges: Timing and scope of patent claims influence market entry barriers for generics.

2. Research and Development Trends

Recent trends indicate increased patent filings focused on biologics, targeted therapies, and combination medicines. If PT3221313 belongs to these categories, the patent landscape could include many overlapping patents, necessitating strategic navigation.

3. Regulatory Environment Impact

EU and Portuguese patent law, with their linkage to patent rights and regulatory data exclusivity, influence how patents like PT3221313 secure and sustain market exclusivity.


Conclusion

The scope of PT3221313, defined primarily by its claims, appears focused on a specific chemical entity or therapeutic method pertinent to the pharmaceutical domain. Its strength depends on claim breadth, prior art, and jurisdictional strategy. The patent landscape surrounding PT3221313 is dense, with competitive forces shaping its enforceability and commercial viability. Understanding these dynamics permits better strategic planning in licensing, R&D, or market entry.


Key Takeaways

  • PT3221313’s claims likely revolve around a novel pharmaceutical compound or method, with scope determined by the chemical or therapeutic specifics.
  • Its enforceability hinges on claim novelty, inventive step, and strategic claim drafting.
  • The patent landscape features many overlapping patents, especially in innovative drug classes, demanding careful freedom-to-operate analysis.
  • International patent filings and potential SPC extensions significantly influence the duration of market exclusivity.
  • Continuous monitoring of new patents or legal developments in Portugal and Europe is critical for safeguarding commercial interests.

FAQs

1. How does PT3221313 compare to other patents in its therapeutic class?
While specific claim details are unavailable here, patents in the same class vary in scope—from broad chemical entities to narrow use cases—tailoring competitive advantages and risk profiles.

2. Can PT3221313 be challenged or invalidated?
Yes. Challenges based on prior art, lack of novelty, or inventive step can threaten validity, especially if competing patents exist.

3. Does PT3221313 have potential patent term extensions?
If granted as a medicinal product patent, it could benefit from SPC protections, extending exclusivity beyond standard 20-year terms.

4. How does the patent landscape affect generic market entry in Portugal?
Strong, broad patents can delay generic entry. Conversely, narrow or weak claims open opportunities once patents expire or are invalidated.

5. What strategic considerations should patent owners pursue for patents like PT3221313?
Owners should consider filing for international protections, monitor competing patents, and strategize around patent claim scope and potential licensing opportunities.


References

  1. INPI Portugal Patent Database. www.inpi.pt
  2. European Patent Office (EPO) Espacenet. Patent number PT3221313.
  3. World Intellectual Property Organization (WIPO) - PATENTSCOPE. Patent family filings and international applications.
  4. European Patent Convention (EPC). Standards for patentability.
  5. Regulations on Supplementary Protection Certificates (SPC) in the EU.

(Note: Specific details such as filing date, inventor, claims, and legal status are assumed or generalized due to limited publicly available data on PT3221313. For thorough analysis, consulting the official patent document is recommended.)

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