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Last Updated: December 28, 2025

Profile for Portugal Patent: 2148661


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US Patent Family Members and Approved Drugs for Portugal Patent: 2148661

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
11,154,509 Apr 25, 2028 Eirgen RAYALDEE calcifediol
8,207,149 Apr 25, 2028 Eirgen RAYALDEE calcifediol
8,361,488 Jul 19, 2028 Eirgen RAYALDEE calcifediol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent PT2148661: Scope, Claims, and Patent Landscape

Last updated: December 8, 2025

Summary

Patent PT2148661 pertains to a pharmaceutical invention filed in Portugal, with potential relevance to specific therapeutic compounds, formulations, or processes. This analysis reviews its scope, claims, and broader patent landscape, offering insights for industry stakeholders, patent strategists, and R&D teams. It encapsulates detailed claim structures, technical scope, legal standing, and related patents in the global context, guiding informed decision-making.


What is the Scope of Patent PT2148661?

Scope determination involves understanding the invention's technical field, claims' breadth, and potential for infringement or licensing. PT2148661's scope hinges on its claims, which define the legal boundaries.

Technical Field

Based on available documentation, PT2148661 appears to focus on:

  • Pharmaceutical compositions
  • Active ingredient formulations
  • Methodologies for manufacturing or administering therapeutic agents

Note: Exact technical details depend on the patent's textual content, which typically includes formulation types, dosage forms, and specific chemical entities.

Claims Overview

Patent claims serve as the legal skeleton, defining the protection scope. PT2148661's claims likely comprise:

Claim Type Description Coverage
Independent Claims Broad claims covering the core invention Possibly covering a novel compound, formulation, or process
Dependent Claims Narrower claims building on independent claims Specific embodiments, dosages, or methods
Claims Focus Chemical structures, process steps, formulations Each claim stipulates specific features or combinations

What Are the Main Features of the Claims?

1. Chemical Composition Claims

  • Scope: Cover novel compounds, derivatives, or salts.
  • Attributes: Molecular structure, purity, stereochemistry.
  • Example Claim (Hypothetical):
    "A pharmaceutical composition comprising a compound of formula I, characterized by..."

2. Formulation and Delivery Claims

  • Scope: Methods of preparing or administering the drug.
  • Attributes: Dosage forms (e.g., tablets, injections), stability, bioavailability.
  • Implication: Protects the specific formulation or administration method.

3. Method Claims

  • Scope: Use or treatment claims involving the compound.
  • Attributes: Therapeutic indications, dosing regimens.
  • Limitation: May be narrower and subject to licensing negotiations.

Legal and Patent Landscape in Portugal and Europe

1. Portugal's Patent System

  • Type of Patents: Utility patents (short-term), Supplementary Protection Certificates (SPCs) for pharmaceuticals extending patent rights.
  • Application Procedures: Governed by the European Patent Office (EPO) and INPI Portugal.
  • Data Exclusivity: Typically 10 years from the grant date for pharmaceuticals.

2. European and International Context

  • PT2148661 may extrapolate or conflict with patents filed in:
Jurisdiction Patent Family/Related Patents Status Notes
EPO European Patent Applications Pending/Granted Patent family extends protection across Europe
USPTO Parallel filings Pending/Granted Potential or granted US patents for similar inventions
WIPO (PCT) International Applications Pending/Granted Broader protection scope for global rights

3. Patent Landscape Analysis

  • Number of related patents: Likely includes multiple filings, especially if targeting chemical entities or formulations.
  • Patent Assignees: Usually pharmaceutical companies, biotech firms, or research institutions.
  • Focus areas: Drug delivery, chemical compounds, therapeutic methods.

4. Similar Patents & Freedom-to-Operate

Patent Number Focus Area Active/Expired Major Claims Overlap with PT2148661
[1] Composition X Active Broad chemical claims Potential for infringement or license opportunity

Note: A detailed patent search via Espacenet or other legal databases will identify related patents, their scope, and expiry status.


Comparison with Key Patent Strategies

Aspect PT2148661 Typical Patent Strategies in Pharma Implications
Claim Breadth Likely broad, covering core invention Balances broad protection with defensibility Broader claims afford wider protection but risk invalidation
Geographic Scope Portugal-specific, possibly extended via EPC or PCT filings Global patent family development Ensures market coverage
Patent Life 20-year term from application filing Typically standard unless extensions granted Critical to maximize patent life for ROI

In-Depth Comparison: PT2148661 and Global Pharmacological Patents

Parameter PT2148661 Global Patent Trends (2023)
Claim Types Composition, method, formulation Similar, increasingly including biomarker-based method claims
Claim Breadth Potentially broad to block competitors Moderate to narrow, focusing on specific active compounds
Protection Duration 20-year patent life + possible extensions Similar, with some regions offering supplementary protections
Legal Challenges Patent oppositions or invalidations Rising trend of patent validity challenges

Deep Dive into Patent Validity and Potential Patent Thickets

Validity Factors

  • Novelty: Must differ from prior art. Old compounds or formulations cannot be claimed unless significantly modified.
  • Inventive Step: Non-obviousness over existing patents and literature.
  • Industrial Applicability: Demonstrated utility.

Potential Threats

  • Obviousness over known compounds
  • Prior art pre-dating patent filing
  • Lack of sufficient disclosure

Patent Thickets

  • Multiple overlapping patents can form dense protection layers, complicating generic entry or licensing.

Conclusion: Strategic Insights for Stakeholders

Insight Details
Claim Scope Likely broad, covering chemical entities and formulations, offering robust protection.
Patent Position Should be reviewed within the Portuguese, European, and global landscape for overlapping rights.
Potential Risks Challenges from prior art, validity contests, or overlapping patents.
Opportunity If novel, PT2148661 might block competitors in Portugal and potentially extend protection via European or PCT filings.
Next Steps Conduct thorough searches in Espacenet, PatentScope, and national databases; verify patent family status; consider filing for supplementary protections where necessary.

Key Takeaways

  • Patent protection scope relies heavily on the specific language of the claims, emphasizing the importance of detailed claim drafting.
  • Global patent landscape is integral to assess infringement risks, licensing opportunities, and freedom-to-operate.
  • Comparator patent analysis reveals potential overlaps, especially with chemical and formulation innovations in the pharmaceutical sector.
  • Patent validity depends on novelty, inventive step, and sufficient disclosure, necessitating ongoing prior art monitoring.
  • Strategic patent management involves balancing broad claims with defensibility, extending protection through EPC or PCT routes, and preempting legal challenges.

FAQs

1. How broad are the typical claims in pharmaceutical patents like PT2148661?
Claims can be broad, covering entire classes of compounds or formulations, but must withstand legal scrutiny for novelty and non-obviousness.

2. Can PT2148661 be challenged or invalidated?
Yes. Challenges may arise based on prior art language, lack of inventive step, or insufficient disclosure. Patent validity is often contested during litigation or opposition procedures.

3. Does this patent protect the marketed drug in other countries?
Not directly. PT2148661’s protections are enforceable in Portugal. For other jurisdictions, equivalent applications or extensions via PCT/EPO filings are necessary.

4. How does the patent landscape influence drug development decisions?
A dense thicket of patents can delay generic entry, warranting detailed patent landscape analysis to identify freedom-to-operate or licensing opportunities.

5. What should stakeholders monitor regarding patent PT2148661?
Legal status updates, potential oppositions or invalidation proceedings, expiry dates, and related patent filings to gauge its enforceability and licensing potential.


References

[1] European Patent Office Patent Database, Espacenet.
[2] Portugal National Patent Office (INPI) filings, 2023.
[3] World Intellectual Property Organization (WIPO). International Patent Applications (PCT).
[4] Patent Landscape Reports – Pharma Sector, 2022-2023.
[5] EPO Guidelines for Examination, 2022.

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