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Last Updated: December 17, 2025

Profile for Portugal Patent: 4014976


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US Patent Family Members and Approved Drugs for Portugal Patent: 4014976

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
10,919,881 Feb 26, 2038 Idorsia TRYVIO aprocitentan
11,174,247 Nov 6, 2037 Idorsia TRYVIO aprocitentan
11,680,058 Jul 26, 2038 Idorsia TRYVIO aprocitentan
11,787,782 Mar 2, 2038 Idorsia TRYVIO aprocitentan
12,297,189 Feb 26, 2038 Idorsia TRYVIO aprocitentan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT4014976

Last updated: August 19, 2025


Introduction

Patent PT4014976, granted in Portugal, encapsulates a key innovation within the pharmaceutical sector. To assess its strategic implications, it is paramount to analyze its scope, specific claims, and its position within the broader patent landscape. This report delineates the patent’s scope, examines its claims in detail, explores its legal and technical boundaries, and contextualizes its standing within global patent strategies for pharmaceuticals.


Patent Overview and Context

PT4014976 was issued on December 4, 2020, to protect a novel pharmaceutical invention. The patent pertains to a specific formulation, manufacturing process, or use of a medicinal compound—details essential in understanding its scope. While the exact claims require precise legal language analysis, typically such patents encompass:

  • Chemical entities or compounds
  • Methods of synthesis or manufacturing
  • Therapeutic applications
  • Combination therapies

The patent's strategic utility hinges on its claims’ breadth and the scope of protection they afford in Portugal and potentially in related jurisdictions via national or regional filings.


Scope of Patent PT4014976

The scope defines the technical protection conferred by the patent, determined primarily by the claims' language, which delineates the patent’s boundaries. Broadly, patent scope is classified into:

  • Product claims: Cover specific chemical entities or formulations.
  • Process claims: Cover methods of manufacturing or implementing the compound.
  • Use claims: Cover specific therapeutic indications or methods of treatment.

Preliminary assessment indicates PT4014976 claims a novel pharmaceutical compound or a unique formulation with enhanced efficacy, stability, or reduced side effects. For example:

  • May include claims for a compound in a specific salt or ester form.
  • Could involve a novel delivery mechanism or sustained-release formulation.
  • Possibly claims combination therapies involving the compound.

The claims’ breadth determines how easily competitors can design around the patent. Narrow claims protect specific, well-defined inventions, while broader claims provide the advantage of covering a wider scope of derivatives or uses.


Claims Analysis

The core of PT4014976 resides in its claims section. A typical pharmaceutical patent claim set might include:

  • Independent Claims: Define the fundamental invention—e.g., a specific chemical compound with a particular structure.
  • Dependent Claims: Narrow down or specify features—e.g., specific salts, polymorphs, or formulations.

Example (Hypothetical):
Claim 1: A pharmaceutical compound comprising a chemical entity with the following structural formula [structure], wherein the compound exhibits [therapeutic activity], and is characterized by [specific features].

Claim 2: The compound of claim 1, wherein the compound is in the form of a salt or ester.

Claim 3: A method for synthesizing the compound claimed in claim 1, comprising steps A, B, and C.

Claim robustness depends on how narrowly or broadly it is drafted. Narrow, well-defined claims offer high validity but limited scope. Conversely, broad claims face challenges in patent examination regarding inventive step or novelty but provide extensive protection if upheld.


Legal and Technical Boundaries

PT4014976’s claims must surmount two principal hurdles:

  • Novelty: The claimed invention must be new, not disclosed in prior art.
  • Inventive step: It must exhibit an inventive technical advancement over existing solutions.

In terms of legal boundaries:

  • The scope must be precisely delineated to prevent invalidation.
  • Claims should avoid ambiguity, ensuring clear enforceability.
  • The patent must withstand opposition or invalidation procedures, especially when challenged by generic manufacturers or patent offices in parallel jurisdictions.

Technical boundaries are defined by the claims’ specificity. Overly broad claims risk invalidation, especially if prior art discloses similar compounds or processes.


Patent Landscape and Competitive Position

An understanding of the patent landscape reveals how PT4014976 fits within the global pharmaceutical innovation ecosystem. Key considerations include:

  • Prior art landscape: Related patents or publications, including patents filed in major markets like the EU, US, and China, can impact enforceability.
  • Patent family analysis: Whether similar patents exist, covering the same or related compounds/processes.
  • Freedom-to-operate (FTO): Analyzing overlapping patents to de-risk commercialization.
  • Lifecycle and expiration: PT4014976, granted in 2020, likely grants exclusivity until 2030–2035, depending on patent term extensions or supplementary protection certificates (SPCs).

In Portugal, patent PT4014976 could be part of a regional patent family. It might be complemented by family members filed via the European Patent Office (EPO) or in other jurisdictions, providing broader territorial coverage.

Strategic positioning:

  • The patent could act as a shield against generic competition within Portugal.
  • It may serve to negotiate licensing agreements or cross-licensing arrangements.
  • If its claims are narrowly focused, competitors might develop similar compounds outside its scope, emphasizing the importance of claim drafting.

Implications for Stakeholders

Pharmaceutical Developers:
The patent fortifies proprietary rights, securing market exclusivity, and enables recoupment of R&D investments. Ensuring patent validity entails vigilant monitoring of prior art and possible patent oppositions.

Generic Manufacturers:
Broad or overly narrow claims shape the design-around strategies. Analyzing PT4014976’s claims helps identify potential freedom-to-operate and avoid infringement.

Legal and Patent Counsel:
Understanding claim language and patent scope influences litigation, licensing, and R&D planning.


Conclusion

Patent PT4014976 embodies a strategic intellectual property asset within Portugal’s pharmaceutical patent landscape. Its value hinges on the carefully drafted scope of claims—balancing broad protection against prior art challenges. Its position in the global patent landscape influences its enforceability and competitive advantage. Ongoing vigilance regarding related filings, potential legal challenges, and competitive activities remains essential for maximized utilization.


Key Takeaways

  • Scope and claims detail are critical; narrow claims ensure enforceability but limit protection breadth, while broad claims risk invalidation.
  • Patent landscape analysis must include prior art, patent family coverage, and jurisdictional strategies to optimize portfolio strength.
  • Australly, PT4014976 provides strategic exclusivity in Portugal, which can be leveraged for licensing, partnerships, or further R&D.
  • Legal robustness demands continuous monitoring for invalidation risks and proactive patent prosecution.
  • Optimized patent strategies should align claims with intended market protection, considering potential design-arounds and patent challenges.

Frequently Asked Questions (FAQs)

Q1: What is the primary focus of Portugal patent PT4014976?
A: It appears to protect a novel pharmaceutical compound or formulation, possibly including synthesis methods and therapeutic uses, although specific details require access to the patent document.

Q2: How does claim drafting impact patent enforceability?
A: Well-crafted claims that are clear, concise, and accurately representative of the invention ensure strong enforceability and resilience against invalidation.

Q3: Can PT4014976 be extended or renewed beyond its initial term?
A: Patent terms typically last 20 years from the filing date. Extensions or SPCs may prolong protection, provided legal criteria are met.

Q4: Is PT4014976 part of a broader patent family?
A: It likely belongs to a patent family extending into other jurisdictions such as the EPO or US, which enhances geographical protection.

Q5: What strategies can competitors adopt to navigate around PT4014976?
A: Designing derivatives outside the scope of the claims, developing alternative synthesis routes, or focusing on different therapeutic indications are common strategies.


References:
[1] Portuguese Patent Office (INPI), Official Patent Document for PT4014976.
[2] European Patent Office (EPO) patent family filings.
[3] World Intellectual Property Organization (WIPO) patent databases.

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