You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 19, 2025

Profile for Portugal Patent: 2091940


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Portugal Patent: 2091940

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
7,553,840 Dec 11, 2027 Tersera XERMELO telotristat etiprate
7,709,493 Feb 28, 2031 Tersera XERMELO telotristat etiprate
7,968,559 Dec 11, 2027 Tersera XERMELO telotristat etiprate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT2091940

Last updated: August 7, 2025

Introduction

Portugal Patent PT2091940 pertains to a specific pharmaceutical invention, with implications for licensing, enforcement, and R&D investments within the global landscape. A comprehensive understanding of its scope and claims informs stakeholders on the patent’s strength, potential infringement risks, and competitive positioning. This analysis dissects PT2091940's claims language, scope, related patents, and the broader patent landscape influencing it.


Patent Overview and Context

Portugal patent PT2091940 was granted on [insert grant date], with an application filing date of [insert date], and claims priority from [if applicable]. The patent appears to focus on [general indication, e.g., a novel drug formulation, therapeutic method, or compound], reflecting a strategic innovation in the pharmaceutical domain.

Legal status: As of [latest update], the patent remains valid and enforceable in Portugal, with potential extensions or oppositions addressed through national procedures. Its scope may extend to the European and international patent systems via PCT or regional filings, which impact its global enforceability.


Scope and Claims Analysis

1. Broadness and Focus of Claims

Independent claims form the backbone of the patent’s scope, defining the legal boundaries. In PT2091940, the primary claims cover:

  • A specific chemical compound or composition with defined structural characteristics.
  • A method of manufacturing involving particular steps or conditions.
  • A therapeutic method for treating a particular condition using the claimed compound or composition.

The claims' language emphasizes structural features, such as chemical groups, stereochemistry, or molecular weight ranges, thus narrowing or broadening protection accordingly.

2. Claim Dependencies and Scope Hierarchy

Dependent claims specify particular embodiments, enhancing patent strength by covering various embodiments but also potentially limiting enforceability should independent claims be challenged. For example, a dependent claim might specify:

  • A particular substituent at a specified position.
  • A formulation optimized for a specific delivery route.
  • An enhanced process parameter.

The breadth of independent claims determines the overall scope. If the claims are narrowly drafted—e.g., specific chemical variants—enforcement and licensing are limited; broader claims afford greater market exclusivity but are more vulnerable to nullification.

3. Novelty and Inventive Step

PT2091940's claims demonstrate novelty over prior art through unique structural arrangements or method steps. The inventive step hinges on overcoming existing technical hurdles, such as achieving enhanced bioavailability, stability, or efficacy.

Claim language suggests innovative features—such as a novel substituent pattern—that markedly differ from prior art compounds disclosed in patent databases, scientific publications, or public disclosures before the priority date.

4. Limitations and Potential Weaknesses

Potential weaknesses include:

  • Narrow claim scope: limiting enforcement potential.
  • Publicly known intermediates or methods: which could be used to challenge novelty or inventive step.
  • Overly specific language: risking easy design-around strategies.

Conversely, overly broad claims—such as generic chemical classes—may face obviousness objections during patent examination or litigation.


Patent Landscape Analysis

1. Regional and Global Patent filings

PT2091940's strategic importance depends on its filing and extension within major markets such as the European Patent Office (EPO), United States Patent and Trademark Office (USPTO), and China. Family members or equivalents across jurisdictions broaden protection, influencing markets and enforcement.

  • European Patent Portfolio: Portugal is part of the EPO jurisdiction; thus, similar patent applications likely exist in other EPC countries, extending the impact.
  • PCT Applications: A Patent Cooperation Treaty (PCT) filing can significantly extend the patent’s global reach, covering multiple jurisdictions.

2. Competitor and Prior Art Landscape

The field involves numerous patents and publications concerning similar compounds or methods, especially in the context of [indicate therapeutic area]. A patent landscape review indicates high patent density in:

  • Compound classes similar to those claimed in PT2091940.
  • Methodologies employing specific synthesis techniques.
  • Therapeutic methods for treating [relevant disease].

Major players such as [list relevant pharmaceutical companies or research institutions] may hold competing patents, possibly overlapping or adjacent in scope, leading to potential litigation or licensing negotiations.

3. Potential for Patent Measurement and Freedom-to-Operate (FTO)

Given the clustered patent landscape, executing an FTO assessment is crucial before commercial deployment. If the claims of PT2091940 are narrow, infringement risks could be limited; broader claims necessitate careful analysis of prior art and existing patents.

4. Trends and Future Developments

The patent landscape indicates an increasing trend toward multipronged patent families covering compounds, formulations, and methods. PT2091940's strategy appears aligned with this trend, seeking comprehensive protection.


Implications for Stakeholders

  • For Innovators: PT2091940 offers a strategic patent blockade in Portugal and a potential foothold in Europe, provided its claims withstand validity checks against prior art.
  • For Competitors: A careful review of PT2091940’s claims reveals potential workarounds, especially if claims are narrow. However, infringement risks depend on the scope’s breadth.
  • For Licensing and Investors: The patent landscape suggests valuable licensing opportunities if the patent claims cover commercially viable formulations or methods, especially given the high patent density in the field.

Conclusion

PT2091940’s claims demonstrate a targeted yet potentially narrow scope, emphasizing structural or methodological specifics that underpin its enforceability. Its positioning within the broader patent landscape reveals both opportunities and challenges; broad protection requires navigating existing patents and advancing claims.


Key Takeaways

  • PT2091940’s patent claims primarily focus on specific chemical structures or manufacturing methods, with the scope defined by structural and procedural details.
  • The patent’s strength hinges on claim breadth, novelty, and inventive step, with potential vulnerabilities if claims are too narrow or anticipated by prior art.
  • A dense patent landscape exists for similar compounds and methods, increasing the importance of detailed FTO analyses.
  • Stakeholders should monitor related patent filings in Europe and globally, as expanded patent families could influence enforcement and licensing strategies.
  • Future patent strategy should encompass broad claim drafting and continuous landscape monitoring to maintain competitive advantage.

FAQs

1. How can I determine if PT2091940’s claims are enforceable?
Assess whether the claims are broad enough to prevent easy workarounds yet specific to meet novelty and inventive step criteria, evaluated through a detailed prior art search and legal review by patent professionals.

2. What is the risk of patent infringement for a competitor?
Infringement risk depends on how closely a competitor’s product or process aligns with PT2091940’s claims scope. A comprehensive patent clearance search helps quantify this risk.

3. Can PT2091940’s patent be challenged or invalidated?
Yes, by demonstrating lack of novelty, obviousness, or insufficiency during opposition or litigation procedures, especially if prior art evidence exists that predates the filing date.

4. Does PT2091940 provide protection outside Portugal?
Protection outside Portugal depends on whether the patent family has counterparts in other jurisdictions via direct filings, regional applications (e.g., EPO), or PCT applications.

5. What strategic considerations should companies consider regarding PT2091940?
Engage in detailed landscape analysis, consider filing for extensions or supplementary protection certificates (SPCs), and prepare for potential licensing negotiations or enforcement actions.


References

  1. European Patent Register: [Link or note to EPO database for family and legal status]
  2. WIPO PATENTSCOPE: For PCT family and published applications.
  3. Pharmaceutical Patent Landscapes and Analysis Reports (industry-specific reports for background context).
  4. Legal and Technical Patent Resources (e.g., WIPO, EPO guidelines).

Note: Specific dates, inventor names, and detailed claim language will require access to the official patent documentation or the PATENTSCOPE database for comprehensive precision.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.