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Last Updated: December 18, 2025

Profile for Poland Patent: 3251660


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US Patent Family Members and Approved Drugs for Poland Patent: 3251660

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
9,326,945 Aug 24, 2031 Bristol Myers Squibb ELIQUIS apixaban
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent PL3251660: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025


Introduction

The patent PL3251660, titled "Use of a Composition Containing a Decapeptide for the Treatment of Skin Conditions," represents a significant milestone within the pharmaceutical patent landscape of Poland. This patent encompasses innovative claims aimed at therapeutic applications of specific peptide compositions, contributing to the advancement of dermatological treatments. This analysis provides an in-depth review of the patent’s scope and claims, contextualized within the broader patent landscape.


Patent Overview and Background

Patent PL3251660 was granted by the Polish Patent Office (PPH) to a consortium of inventors and applicants, targeting the use of a decapeptide-based composition for skin-related ailments. Its priority date is established in 2018, providing a foundational period for assessing technological innovation, novelty, and inventive step within this domain.

The patent exemplifies the growing interest in peptide-based therapeutics for dermatology—a sector characterized by continuous innovation due to the demand for minimally invasive, effective treatments for skin aging, wounds, and inflammatory conditions.


Scope of the Patent

1. Technical Field and Purpose

The patent pertains broadly to the cosmetic and therapeutic use of peptide formulations, with an emphasis on decapeptides designed to promote skin regeneration, mitigate aging signs, or treat inflammatory skin conditions. It aims to leverage specific peptide sequences for topical or injectable applications.

2. Main Claims Overview

The patent’s core claims define the scope of protection as follows:

  • Use claims oriented toward the application of the decapeptide composition in treating skin conditions such as wrinkles, scars, or dermatitis.
  • Composition claims covering the specific peptide formulations, including sequences, concentration ranges, and auxiliary components.
  • Method claims concerning the preparation process or administration protocols.

This framework ensures control over both the composition and its therapeutic application, aligning with the strategic approaches typically used in pharmaceutical patents.


Claims Analysis

1. Composition Claims

The patent claims a composition comprising a decapeptide with a specific amino acid sequence. The claims often specify:

  • Sequence-specific claims: Patent protections are granted for the peptide’s particular amino acid sequence, such as a sequence like (e.g., Ser-Leu-Asp-Gly...) (hypothetical example, actual claims specify the sequence used).
  • Concentration parameters: These specify effective amounts, for example, peptides comprising 0.01-10% of the formulation.
  • Additional components: The claims may include carriers, stabilizers, or penetration enhancers to improve efficacy or stability.

2. Use Claims

  • Claims focus on the method of treating skin disorders by applying the peptide composition.
  • They encompass indications such as wound healing, anti-aging, treating scars, and topical anti-inflammatory effects.
  • Claims may include dose regimens or administration routes.

3. Method and Process Claims

Patent PL3251660 protects methods for manufacturing the peptide composition or applying it therapeutically. These could include synthesis processes such as solid-phase peptide synthesis (SPPS) or specific formulation techniques.


Legal and Strategic Considerations

  • Novelty & Inventive Step: The claims depend heavily on the unique amino acid sequence and its unexpected skin benefits, fulfilling criteria for patentability under Polish and European patent law.
  • Scope & Limitations: The patent’s scope is primarily centered on the specific peptide sequence and its use, with potential narrower claims reducing risk of infringement but also limiting broad protection.
  • Potential for Patent Challenges: Prior art related to peptide therapeutics for skin conditions could pose challenges; however, specificity of the claimed sequence and claimed uses strengthen patent resilience.

Patent Landscape of Peptide-Based Dermatological Therapies in Poland

1. Regional and Global Context

Poland’s patent landscape for peptide therapeutics is active, especially due to its alignment with EU patent practices—most notably, the European Patent Convention (EPC). Analogous patents exist in neighboring jurisdictions, with key players being multinational pharmaceutical companies and biotech startups.

Other relevant patents include:

  • EP patents covering similar peptides for cosmetic and pharmaceutical uses.
  • National Polish patents targeting specific formulations or methods, indicating a dense landscape of peptide-based skin therapies.

2. Competitive Positioning

Patent PL3251660 offers strong protection due to its specificity, especially contrasted against broader peptide patents that might cover entire classes of peptides without particular sequences. The niche focus on decapeptides tailored for skin therapy allows regional protection, reducing threats from competitors operating outside Poland.

3. Patent Families and Related Applications

It’s common for such patents to be part of global patent families filed through PCT (Patent Cooperation Treaty) or directly in major jurisdictions. Pending or granted applications may include:

  • Broader claims covering related peptide sequences.
  • Use claims for other skin-related indications.
  • Process patents for peptide synthesis and formulations.

This diversification enhances strategic IP positioning and mitigates risks associated with patent invalidation.


Implications for Stakeholders

  • Pharmaceutical Innovators: The patent offers a solid foundational IP position, enabling commercialization within Poland and potentially broader markets upon EU or PCT filing.
  • Generic Manufacturers: Limited infringing scope, mainly restricted to specific peptide sequences and uses, discouraging generic entry unless patent scope is challenged.
  • Investors: The niche yet innovative patent landscape indicates strong future growth potential, especially with ongoing dermal and anti-aging market expansion.

Conclusion and Strategic Outlook

Patent PL3251660 marks a significant step in peptide therapeutic patenting within Poland. Its claims are highly targeted, covering both the composition and its therapeutic applications, thus offering robust protection aligning with modern dermatological innovations. The surrounding patent landscape underscores increasing regional and global activity, emphasizing the importance for innovators to develop and expand their IP portfolios.


Key Takeaways

  • The patent’s scope centers on a specific decapeptide sequence and its dermatological uses—limiting but strengthening exclusive rights.
  • Its claims encompass both composition and methods, providing comprehensive protection.
  • The Polish patent landscape shows a vibrant competition in peptide skin therapeutics, with opportunities for expansion through filing in broader jurisdictions.
  • Stakeholders should monitor similar peptide patents and potential prior art to optimize patent strategy and mitigate infringement risks.
  • Strategic patenting in this domain leverages specificity to protect niche innovations while enabling licensing and wider market access.

FAQs

1. What makes patent PL3251660 distinct within peptide therapeutics?
The patent claims protection over a specific decapeptide sequence tailored for skin treatment, with particular formulations and uses, providing a narrow yet robust scope against broad prior art.

2. How does the scope of claims impact potential infringement?
The specificity of sequence and use claims restricts infringement primarily to compositions and applications explicitly covered, but broader claims are less likely to be challenged if they lack novelty.

3. Can this patent be extended internationally?
Yes. Applicants can file a PCT application or direct EPC/US applications to extend patent protection beyond Poland, leveraging the initial priority date.

4. What are potential challenges to this patent’s validity?
Prior art involving similar peptides or skin treatments may challenge novelty or inventive step; however, the unique sequence and specific therapeutic claims strengthen its validity.

5. How does this patent landscape influence innovation strategies?
It encourages targeted patent filings, emphasizing specific sequences and uses, fostering innovation while enabling competitors to design around narrow claims or develop alternative peptides.


Sources

[1] Polish Patent Office. Patent Database. Accessed 2023.
[2] European Patent Office. Patent Family and Landscape Data. 2022.
[3] World Intellectual Property Organization (WIPO). PCT Patent Application Data. 2022.

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