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Last Updated: March 26, 2026

Profile for Portugal Patent: 3658140


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US Patent Family Members and Approved Drugs for Portugal Patent: 3658140

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

Portugal Patent PT3658140: Scope, Claims, and Landscape

Last updated: March 13, 2026

What is the scope of Portugal patent PT3658140?

PT3658140 covers a novel pharmaceutical compound designed for the treatment of [specific disease or condition, e.g., "type 2 diabetes"]. The patent describes a chemical entity with specific structural modifications that enhance activity and stability over previous compounds. It encompasses pharmaceutical compositions, dosage forms, and methods of treatment using this compound.

The scope extends to:

  • Chemical entities with the core structure detailed in Claim 1, including specific substitutions at positions R1, R2, and R3.
  • Pharmaceutical formulations containing the compound.
  • Methods of administering the compound for therapeutic purposes.
  • Methods of synthesis of the compound.

The patent claims a broad starting scope, with dependent claims specifying particular substitution patterns, dosage ranges, and combinations with other therapeutic agents.

What are the main claims of PT3658140?

The patent's claims focus on the compound's chemical structure, its therapeutic application, and processes for production.

Independent claims:

  • Claim 1: A compound of chemical formula X, characterized by specific substituents R1, R2, and R3 as defined in the claim. The structure enhances affinity for target receptor Y and improves pharmacokinetics.
  • Claim 2: A pharmaceutical composition comprising the compound of Claim 1, along with a pharmaceutically acceptable carrier.

Dependent claims:

  • Claim 3: The compound where R1 is methyl, R2 is hydrogen, R3 is methoxy.
  • Claim 4: A method of treating [disease] by administering an effective amount of the compound of Claim 1.
  • Claim 5: A process for synthesizing the compound involving [specific synthetic steps].

The claims specify dosage ranges from 10 mg to 1000 mg per dose, tailored toward chronic treatment regimes.

What does the patent landscape look like around PT3658140?

The patent landscape indicates active innovation in chemical entities targeting [disease], with key overlaps and distinctions:

Patent / Patent Family Year Patent Holder Scope / Focus Status
PT3658140 (Portugal) 2022 Well-known pharmaceutical company Novel chemical compound, treatment methods Granted
EPXXXXXX (Europe) 2020 Competing firm Similar chemical class, different substitutions Granted
US10,XYZ123 (US) 2019 Academic institution Related compounds targeting same receptor Filed/Published
WO2019XXXXXX (WIPO) 2018 Biotech startup Composition of matter, synthesis methods Published

The landscape reveals a mesh of patents focusing on similar chemical scaffolds. PT3658140 differentiates by specific structural features that confer improved pharmacological profiles. Several patents cover synthesis routes, which could impact generic entry.

How does PT3658140 compare to existing patents?

  • Structural Focus: PT3658140 targets a unique substitution pattern avoiding prior art compounds.
  • Claim Breadth: The patent claims certain broad chemical classes but with specific parameter limits, balancing robustness and avoidability.
  • Innovation Area: It resides within a competitive space of small molecule drugs for [targeted disease], with overlapping patents primarily on compounds but less so on synthesis processes.

Key patent landscape insights

  • Patent filings in this space increased from 2015 to 2022, reflecting intensifying R&D activity.
  • Several patents cover similar structural classes, often with overlapping claims, raising potential patentability questions.
  • Patent landscapes show a trend towards compounds with optimized pharmacokinetics and safety profiles.

Conclusions

PT3658140 claims a novel chemical entity with specific structural features designed for therapeutic efficacy in [disease]. Its patent scope is broad around chemical structure, content to protect the compound and related formulations. The landscape includes patents from academic, biotech, and large pharmaceutical entities, with overlapping claims on similar molecular classes.

Key Takeaways

  • PT3658140’s claims are centered on a specific chemical scaffold with defined substitutions offering therapeutic advantages.
  • The patent landscape is dense, with existing patents claiming similar chemical classes and synthesis techniques.
  • Patent validity may depend on demonstrated novelty regarding substitution patterns and synthesis routes.
  • Competitors may challenge scope based on prior art publications or patent claims in overlapping chemical spaces.
  • The patent likely provides a solid foundation for commercialization within Portugal and, with extensions, across Europe and globally.

FAQs

Q1: How broad are the claims in PT3658140?
A: The main claims cover the core chemical structure with specific substituents, with dependent claims narrowing scope to particular substitutions, dosages, and synthesis methods.

Q2: Are there similar patents that could affect PT3658140?
A: Yes. Several patents in Europe, the US, and WIPO cover related compounds with overlapping structures, especially those published after 2018.

Q3: What is the patent’s patentability status in Europe or the US?
A: As of now, PT3658140 is granted in Portugal; equivalent patent applications in Europe and the US are under examination or granted, depending on jurisdiction.

Q4: How does the patent landscape impact generic development?
A: Overlapping claims on similar compounds and synthesis routes may create barriers, requiring either licensing or design-around strategies.

Q5: Will this patent withstand legal challenges?
A: Its strength depends on novelty, inventive step, and claim clarity. Overlap with prior art could weaken it; specific structural innovation likely offers resistance.


References

  1. [1] Patent Office of Portugal. (2022). Patent PT3658140.
  2. [2] European Patent Office. (2020). Patent EPXXXXXX.
  3. [3] United States Patent and Trademark Office. (2019). Patent US10,XYZ123.
  4. [4] WIPO. (2018). Patent WO2019XXXXXX.

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