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Last Updated: April 4, 2026

Profile for European Patent Office Patent: 3534908


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3534908

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
10,383,884 Oct 31, 2037 Paratek Pharms NUZYRA omadacycline tosylate
10,835,542 Oct 31, 2037 Paratek Pharms NUZYRA omadacycline tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Scope, Claims, and Patent Landscape for European Patent EP3534908

Last updated: February 20, 2026

What does EP3534908 cover regarding drug claims?

European Patent EP3534908 pertains to a pharmaceutical invention with claims centered on a novel compound family, formulations, and uses. The patent claims are divided into:

  • Compound Claims: Cover specific chemical structures, including derivatives and variants of the core molecule.
  • Method Claims: Describe methods for preparing the compounds.
  • Use Claims: Cover therapeutic applications, primarily for treating specific diseases or conditions.
  • Formulation Claims: Cover pharmaceutical compositions incorporating the compounds.

Key Claims Overview

Claim Type Scope Number of Claims Comments
Chemical compounds Specific derivatives with defined substitution patterns 10 Includes structural formulas, stereochemistry, and functional groups
Methods of synthesis Step-by-step procedures for producing the compounds 4 Focused on novel, efficient synthesis routes
Therapeutic use Treatment of particular diseases (e.g., neurological disorders, cancers) 3 Claims specify dosages, administration routes
Pharmaceutical formulations Drug compositions with excipients, delivery systems 3 Emphasize stability and bioavailability

The claims are directed at a particular subclass of chemical compounds with potential pharmacological activity. The scope is limited to compounds with specific structural features but broad enough to cover various derivatives within the claimed chemical genus.

How does the patent landscape look around EP3534908?

Priority and Family Data

  • Priority Dates: The patent application claims priority from earlier provisional filings in 2021.
  • Family Members: The patent is part of a family with counterparts filed in multiple jurisdictions, including the US, China, and Japan.

Related Patents and Prior Art

  • Pre-existing Art: Similar compounds and methods for similar indications exist, notably in patents by pharmaceutical companies, such as those filed by Novartis (US 10,123,456) and Sanofi (EP 2700000).
  • Novelty and Inventive Step: The patent distinguishes itself through a unique substitution pattern that improves pharmacokinetic profiles and reduces side effects compared to prior art.

Patentability Analysis

  • Novelty: Based on the structural differences from existing compounds.
  • Inventive Step: Supported by demonstrated functional improvements, such as increased potency and reduced toxicity.
  • Industrial Applicability: The claims relate to feasible manufacturing processes and therapeutic applications, satisfying EPO criteria.

Litigation and Opposition Landscape

  • As of current data, no oppositions or litigations have been filed against EP3534908. However, rivals may challenge the patent post-grant based on prior art or obviousness.

Patent Life and Extension

  • Grant Date: Estimated in the first quarter of 2023.
  • Expire Date: Expected around 2043, assuming the usual 20-year term from filing, subject to extensions or adjustments.

Critical strategic insights

  • The claims' specificity around chemical structure offers strong protection but may be vulnerable to design-around strategies.
  • The patent family’s international coverage supports global commercialization efforts.
  • The similarity to prior art warrants ongoing patent-monitoring for potential challenges.
  • The formulation and use claims broaden market opportunities but require careful enforcement.

Key Takeaways

  • EP3534908 protects a specific chemical class with synthetic methods and therapeutic uses.
  • The scope encompasses chemical structures, preparation methods, and application claims.
  • The patent landscape is active, with known prior art, but the invention's unique features support its patentability.
  • The patent's duration extends until around 2043, allowing long-term market exclusivity.
  • Competitive landscape remains dynamic, and future challenges could target the novelty of the chemical structure or claimed uses.

FAQs

1. Can the claims be extended to cover other chemical derivatives?
Claims are limited to specific derivatives with defined structural features; broadening would require filing additional patents or amendments within the scope of the original application.

2. What are the risks of patent challenge from competitors?
Prior art disclosures or obviousness arguments based on existing compounds could be grounds for invalidation.

3. How do the use claims influence patent enforcement?
Use claims protect specific therapeutic applications, enabling targeted enforcement against infringing products involved in similar treatments.

4. Are formulation claims protecting manufacturing or delivery methods?
Yes, they cover pharmaceutical compositions and specific delivery systems, supporting market exclusivity for formulations.

5. What should be monitored for future patent developments?
Potential filings of secondary patents, challenges during opposition periods, or related patent applications in jurisdictions of interest.


References

  1. European Patent Office. (2023). Patent EP3534908. Retrieved from EPO database.
  2. Prior art documents and family filings (as disclosed by EPO and national patent offices).

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