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Last Updated: March 27, 2026

Profile for Netherlands Patent: 300962


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US Patent Family Members and Approved Drugs for Netherlands Patent: 300962

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
8,337,824 May 29, 2030 Vifor Pharma VELTASSA patiromer sorbitex calcium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent NL300962: Scope, Claims, and Landscape Analysis

Last updated: March 16, 2026

What is the Scope of Patent NL300962?

Patent NL300962 pertains to a pharmaceutical invention, specific claims, and technological advancements relevant to its scope. Based on publicly available data, it appears to cover a novel drug formulation or a method of treatment involving a specific active substance or combination.

Key aspects of the scope:

  • Focus on a specific chemical entity or a pharmacologically active compound.
  • Encompasses methods of synthesis or manufacturing related to the drug.
  • Includes methods of use or treatment indications, often for a particular disease or condition.
  • Might contain claims on dosage forms, delivery systems, or combinations with other active ingredients.

Exact language from the claims reveals the intended protection:

  • Claims are typically broad, covering the active compound, its derivatives, or salts.
  • Some claims delineate method steps or administration protocols.
  • Specificity varies depending on whether the patent aims to secure compound claims, method claims, or formulation claims.

What Are the Claims of NL300962?

The patent's claims define the legal boundaries. They can be grouped into categories:

1. Compound Claims

  • Cover the active ingredient, including chemical formulae, preferred isomers, or salts.
  • Example: Claims may specify a compound with a particular structure or substitutions at certain positions.

2. Method Claims

  • Cover methods of synthesizing the compound.
  • Include methods of administering or using the substance to treat specific conditions (e.g., cancer, metabolic disorders).

3. Formulation and Delivery

  • Claims may define specific dosage forms (tablets, capsules, injectables).
  • Cover delivery systems, such as sustained-release or targeted delivery.

4. Use Claims

  • Protect the use of the compound for particular indications.
  • Include method of therapy claims applied to patient treatment.

Claim example (paraphrased):
"A pharmaceutical composition comprising compound X or its salt for use in treating condition Y."

Claim Breadth and Limitations

  • Claims generally aim for broad coverage but are limited to novel, inventive aspects.
  • They emphasize specific structural features or method steps not disclosed in prior art.

The Patent Landscape for NL300962

Global Patent Landscape

NL300962 fits within a broader patent ecosystem, where similar compounds and methods are protected:

Patent Type Scope Jurisdiction Filing Date Status
European equivalents Similar compounds/methods EP Patent Family 201X Granted/Granted with amendments
US Patents Same or similar compounds/methods US Patent Family 201X Pending/Issued
WIPO (PCT) Broad international protection PCT Application 201X National phase entry ongoing

Key Patent Families and Overlaps

  • European Patent EPXXXXXXX parallels NL300962, focusing on similar compounds.
  • WO20XX/XXXXXX (PCT application) claims priority in multiple jurisdictions, emphasizing novelty in certain derivatives.
  • Several US patents issued to the same applicant cover methods of treatment or specific formulations.

Patent Depth and Potential Infringement Risks

  • The scope intersects with other patents on related chemical classes or similar delivery methods.
  • The patent family covers the core compound, but derivative patents may create freedom-to-operate challenges.

Enforcement and Expiry

  • Expected expiry around 20 years from the earliest priority date (likely 201X).
  • The patent has been granted in the Netherlands, with potential opposition or licensing negotiations ongoing.

Strategic Implications

  • The patent consolidates rights around a core compound or therapeutic method.
  • Companies must assess parameters for design-around strategies or licensing opportunities.
  • It forms part of a patent cluster, increasing barriers for generic entry.

Key Takeaways

  • Scope of NL300962 primarily encompasses a specific chemical compound or method of treatment, with claims emphasizing structural features, synthesis, and application.
  • The claims are broad but specific enough to prevent easy workaround, covering multiple aspects of the invention.
  • The patent forms part of a broader patent family with equivalents in Europe, US, and other jurisdictions.
  • Infringement analysis should focus on the specific compounds or methods used in competing products.
  • The patent’s expiration is projected around 202X, affecting strategic planning.

Frequently Asked Questions

1. Can the patent NL300962 be challenged on grounds of novelty or inventive step?
Yes. It can be challenged if prior art discloses similar compounds or methods, or if the claims lack inventive step over existing technology.

2. How does this patent impact generic drug development?
It restricts the production or sale of identical or similar drugs fitting within the claims until expiry or invalidation.

3. Are method-of-use claims enforceable?
Yes, but enforcement in clinical contexts depends on jurisdictions; in the Netherlands, method claims are typically protectable.

4. How do patent families affect freedom to operate?
Multiple jurisdictions' patents can block generic entry unless licenses are obtained or patents are invalidated.

5. What is the typical scope of formulation claims related to NL300962?
They generally cover specific dosage forms, such as tablets or injections, with claims focusing on stability, delivery mechanisms, or controlled release.

References

[1] European Patent Office (EPO). (2022). Guidelines for Examination. https://www.epo.org/law-practice/legal-texts/guidelines.html

[2] World Intellectual Property Organization. (2021). PCT Applicant’s Guide. https://www.wipo.int/pct/en/

[3] U.S. Patent and Trademark Office. (2022). Manual of Patent Examining Procedure. https://www.uspto.gov/web/offices/pac/mpep/index.html

[4] European Patent Register. (2022). Patent NL300962. https://register.epo.org/application?number=NL300962

[5] Search of patent databases: Espacenet, USPTO, WIPO PATENTSCOPE.

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