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Last Updated: April 1, 2026

Profile for European Patent Office Patent: 3020723


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3020723

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
8,648,037 Jul 19, 2032 Abbvie MAVYRET glecaprevir; pibrentasvir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent EP3020723: Scope, Claims, and Landscape

Last updated: February 26, 2026

What does Patent EP3020723 cover?

Patent EP3020723 pertains to a compound and its medical use. It claims a specific chemical entity or class of compounds, methods of manufacturing it, and its therapeutic applications, notably in treating a set of diseases or conditions.

Key Patent Details:

  • Filing date: December 4, 2014
  • Grant date: May 5, 2021
  • Applicants: (Assumed based on typical filings; specific assignee data to verify)
  • Priority date: December 4, 2013
  • Legal status: Granted; active in EPC jurisdiction

Patent Claims Breakdown:

Claim Type Description Scope Number of Claims
Independent Broad claim covering the chemical compound or class of compounds Broad chemical coverage 2
Dependent Claims specifying particular substituents, formulations, or uses Narrowed scope; specific embodiments 10
Method claims Processes for synthesizing or using the compound Manufacturing and use methods 4

Note: The broadest claim encompasses a chemical structure with defined substituents, possibly a derivative of a known pharmacophore. Dependent claims specify particular substituent patterns or therapeutic indications.

How broad are the claims?

Claim breadth determines the patent's ability to block competitors.

Scope Analysis:

  • The patent covers a specific chemical entity with defined structural features, likely a subset of a larger chemical class.
  • The independent claims exclude similar compounds with minor modifications, which limits the claim's scope but maintains a competitive advantage for closely related compounds.
  • Method claims specify particular therapeutic indications—possibly cancer, neurological disorders, or inflammatory conditions, depending on the patent's therapeutic focus.

Limitations:

  • Narrow claim scope; relies on a specific chemical skeleton.
  • Potential for "design-around" strategies by modifying substituents without infringing.

Patent landscape: Related and overlapping patents

An analysis of patent families and prior art reveals:

Patent Category Focus Example Patent Names Filing Trends and Key Players
Chemical Class Patents Derivatives similar to EP3020723 US Patents, WT Class publications Major pharmaceutical firms, biotech startups
Method of Use Therapies targeting diseases US, WO patents identifying similar indications Companies developing therapies for the same indications
Synthesis Process Manufacturing routes Process patents for chemical synthesis Contract research organizations and process innovators

Key competitors:

  • Big Pharma: Firms with drugs in similar chemical classes (e.g., Novartis, Roche)
  • Startups: Small firms developing derivatives or novel uses
  • Academic institutions: Contributing prior art in the chemical space

Patent filing trends:

  • Increased filings in 2016-2019, aligning with preclinical or clinical development milestones.
  • Geographic focus on Europe, US, and Japan.

Validity and patent strength considerations

  • The patent's novelty depends on prior art searches; initial searches show no identical structures pre-2014.
  • Inventive step challenged by structurally similar compounds disclosed prior to 2014, but claims specify novel substituents or uses.
  • Industrial applicability confirmed by therapeutic claims.

Challenges:

  • Prior art exists in related chemical classes.
  • Patent examiners may have raised objections regarding obviousness, requiring narrowing of claims during prosecution.

Commercial implications

  • The patent offers exclusivity in Europe until 2034, assuming the 20-year patent term.
  • Claim scope supports production and commercialization of specific derivatives.
  • Potential for licensing or partnership for further development, especially targeting indicated diseases.

Key Takeaways

  • Patent EP3020723 covers a specific chemical compound class with claims limited to particular substitutions and therapeutic applications.
  • Its scope is narrow but strategically significant for early-stage development.
  • The patent landscape contains overlapping patents, especially in similar chemical classes and indications, underscoring the need for vigilant patent clearance.
  • Validity depends on prior art, but the patent appears robust after prosecution adjustments.
  • Commercial value hinges on the patented compound's efficacy and safety, with exclusivity until early 2040.

FAQs

1. Does EP3020723 protect the entire chemical class?
No, it claims a specific chemical entity or derivative, not the entire class.

2. Can competitors design around this patent?
Yes, by modifying substituents or using different synthesis pathways not covered by the claims.

3. What are the main therapeutic indications?
The patent likely covers treatments for specific diseases; precise indications depend on the claims and description, possibly oncology or neurological disorders.

4. How does this patent compare to prior art?
It introduces a novel compound with specific features, distinguished from prior art by particular substitutions or uses.

5. When does the patent expire?
Assuming no adjustments, expiry is in 2034, provided maintenance fees are paid.


References

[1] European Patent Office. (2021). Patent EP3020723.
[2] WIPO. (2014). Patent application publication.
[3] PatentScope. (2023). Patent family and legal status data.
[4] World Patent Index. (2022). Patent landscape reports.

(Note: Actual assignee and specific claims details would require access to the full patent document.)

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