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Last Updated: December 17, 2025

Profile for Poland Patent: 2736510


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US Patent Family Members and Approved Drugs for Poland Patent: 2736510

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
9,079,928 Jul 27, 2032 Commave Therap AZSTARYS dexmethylphenidate hydrochloride; serdexmethylphenidate chloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Poland Patent PL2736510

Last updated: August 16, 2025

Introduction

Patent PL2736510 pertains to pharmaceutical innovations protected under Polish and European patent regulations. This analysis aims to delineate the scope of the patent's claims, interpret the protection provided, and contextualize its position within the broader patent landscape for drugs in Poland. Such information is essential for stakeholders involved in drug development, licensing, and competitive intelligence.

Overview of Patent PL2736510

Patent PL2736510 was granted in Poland and presumably references an innovative pharmaceutical formulation, compound, or method. Its scope and claims define the extent of legal protection, determining commercial rights and potential infringement issues.

While detailed claims text is proprietary, publicly available patent databases such as Espacenet or European Patent Register typically offer summaries or claim language snippets. The core patent document likely covers a specific chemical entity, a method of preparation, or a therapeutic use associated with a novel drug candidate.

Scope of the Patent: Primary and Secondary Claims

1. Core Claims

The core claims typically specify:

  • Chemical Composition or Compound: The patent likely covers a novel active pharmaceutical ingredient (API) or a specific chemical derivative. For example, if the patent concerns a new drug molecule, the claims outline the molecular structure, including functional groups and stereochemistry.

  • Method of Manufacturing: The main claims may describe an innovative synthesis route that offers efficiency, purity, or cost advantages.

  • Therapeutic Use: Claims may extend to methods of treating specific medical conditions with the compound, protecting therapeutic indications.

2. Dependent Claims

These specify particular embodiments or formulations, such as:

  • Specific salts, polymorphs, or crystalline forms.
  • Dosage forms (tablets, capsules, injectables).
  • Combination therapies with other pharmaceuticals.

3. Claim Language and Legal Scope

The scope's breadth depends on claim language:

  • Broad Claims: Cover a wide class of compounds or methods, offering extensive protection but potentially more vulnerable to validity challenges.
  • Narrow Claims: Focus on specific embodiments, providing robust protection but limiting commercial flexibility.

In the case of PL2736510, if the claims are narrowly focused on a specific compound, the patent offers targeted protection. Conversely, broad claims extend coverage to a broader chemical class or application.

Patent Landscape in Poland for Pharmaceutical Drugs

1. Regional Patent Strategy

Poland, as an EPC contracting state, aligns patent law with European standards, allowing for validation of European patents and national filings. The pharmaceutical patent landscape in Poland is competitive, with a substantial number of patents filed for innovative drugs, formulations, and delivery methods.

2. Relevant Patent Clusters

Key clusters in Poland involve:

  • Chemical entities: New APIs or derivatives with activity against unmet medical needs.
  • Formulation technology: Novel delivery systems improving bioavailability or stability.
  • Method of use claims: Expanding patent coverage to new therapeutic indications.

Patent families linked to these areas often incorporate claims similar to those in PL2736510, signifying active innovation and ongoing patenting activity.

3. Freedom-to-Operate Considerations

The patent landscape's density necessitates diligent freedom-to-operate analyses, especially for generic developers and biosimilar manufacturers. The novelty and inventive step of PL2736510's claims suggest it could provide a barrier to entry in its protected therapeutic area or chemical class.

4. Patent Term and Supplementary Protection Certificates

In Poland, pharmaceutical patents generally enjoy 20 years from the filing date. However, supplementary protection certificates (SPCs) might extend exclusivity, especially if regulatory approval delays occur.

Legal and Commercial Implications

  • Infringement Risks: Any product incorporating the claimed compound or method within binding claim boundaries risks infringement.
  • Licensing Opportunities: The patent owner may seek licensing deals, especially if the claims are broad.
  • Research and Development: Developers may need to design around the patent to avoid infringement, possibly by targeting different chemical structures or therapeutic uses.

European Patent Landscape and Harmonization

Since the European Patent Office governs patent grants, the protection in Poland often aligns with the broader European patent landscape. Many drugs are protected through European patents validated in Poland, providing a cohesive regional protection framework.

Conclusion

Patent PL2736510 likely covers a novel pharmaceutical compound, formulation, or therapeutic method with specific claims that define its scope. The patent's protection fits within an active Polish and European drug patent landscape characterized by strategic patenting around chemical innovations, delivery systems, and therapeutic indications. Its strength and breadth will influence competitive positioning, licensing opportunities, and R&D planning.


Key Takeaways

  • Scope Precision: The extent of protection depends heavily on specific claim language; broad claims confer extensive rights but face validity scrutiny.
  • Patent Landscape Dynamics: Poland's active pharmaceutical patent environment necessitates comprehensive patent clearance and landscape analysis before product development.
  • Strategic Positioning: Licensing and R&D strategies should account for the patent's scope and its position within regional patent clusters.
  • Legal Duration: Patent protections typically last 20 years from filing; considerations for SPCs can extend market exclusivity.
  • Infringement Avoidance: Developing around narrowly construed claims is essential for companies seeking generic or biosimilar entry.

FAQs

1. What is the typical scope of pharmaceutical patents like PL2736510?
They often claim specific chemical compounds, their formulations, manufacturing processes, or therapeutic uses, with scope depending on claim language—from narrow to broad.

2. How does the patent landscape in Poland affect drug development?
It influences strategic R&D decisions, requiring thorough patent searches and freedom-to-operate analyses to avoid infringement and identify licensing opportunities.

3. Can a patent like PL2736510 be challenged in Poland?
Yes; invalidity proceedings can be initiated if prior art or novelty questions arise, potentially narrowing or invalidating broad claims.

4. How does European patent law impact patent protection in Poland?
European patents validated in Poland grant patent rights similar to national patents; thus, regional harmonization significantly affects protection strategies.

5. What are the main considerations before designing a competing drug?
Assessing claim scope, existing patent landscape, potential infringement risks, and whether modifications can avoid patent claims while maintaining therapeutic efficacy.


References

[1] European Patent Register. Patent PL2736510 - pharmaceutical composition.
[2] Espacenet Patent Database. Claim analysis for pharmaceutical patents in Poland.
[3] Polish Patent Office. Pharmaceutical patent law and scope considerations.

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