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Last Updated: December 29, 2025

Profile for Poland Patent: 3169307


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US Patent Family Members and Approved Drugs for Poland Patent: 3169307

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
⤷  Get Started Free Jan 14, 2036 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
⤷  Get Started Free Jul 17, 2035 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
⤷  Get Started Free Jul 17, 2035 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Drug Patent PL3169307

Last updated: August 14, 2025

Introduction

Poland patent PL3169307, titled “Method of treating or preventing cancer or tumor”, represents a significant intellectual property asset within the oncology pharmaceutics domain. This patent encompasses specific therapeutic methods targeting cancer, highlighting both innovative composition and treatment claims. This analysis delineates the patent's scope and claims, examines its position within the broader patent landscape, and discusses strategic implications for industry stakeholders.

Patent Overview

PL3169307 was granted by the Polish Patent Office, with priority claimed from several related patent applications, possibly including international filings. The patent’s priority date, filings, and expiration details provide crucial context for understanding its relevance amid evolving patent landscapes (as of early 2023, patents in Poland are typically valid for 20 years from the earliest priority date).

Scope of Patent

The scope of PL3169307 is focused on a novel therapeutic method involving specific agents or regimens for the treatment or prevention of cancer. The claims emphasize the application of particular compounds, combinations, or dosing schedules designed to improve efficacy, reduce side effects, or address resistant tumor types.

Key Aspects of the Scope

  • Therapeutic Methodology: The patent claims a method involving administering a specific compound or combination thereto, aimed at cancer cells. This includes specific dosage forms, routes of administration, and potential combination therapies.

  • Targeted Cancer Types: The patent indicates broad applicability across various tumor types, potentially including solid tumors, hematological malignancies, or specific subtypes. The detailed specification describes mechanisms of action pertinent to particular molecular pathways.

  • Active Ingredients: Incorporates specific chemical entities—likely small molecules, biologics, or targeted therapies—defined with chemical formulas or known identifiers, such as kinase inhibitors, immune modulators, or novel agents.

  • Innovative Features: May include novel methods of delivery, synergistic combinations, or unique treatment regimens aimed at overcoming drug resistance or enhancing treatment outcomes.

Claims Analysis

The patent’s claims are core to understanding its legal scope and enforceability. Both independent and dependent claims structure the boundaries of proprietary rights.

Independents Claims

  • Method of Treating Cancer: Typically, an independent claim defines a method involving administering an effective amount of a compound or combination to a patient, resulting in tumor regression or prevention. Such claims are broad, attempting to cover all uses of the compound in the specified cancer context.

  • Composition of Matter: Claims could also encompass the active chemical entity itself, broadly covering the compound irrespective of specific indications.

  • Combination Claims: Claims may specify the use of the compound with other agents, e.g., chemotherapeutics, immunotherapies, or adjuvants, emphasizing synergistic effects.

Dependent Claims

Dependent claims narrow the scope, specifying particular dosages, forms, or treatment protocols (e.g., specific dosages, timing, or administration routes). They provide fallback positions if broader independent claims are challenged.

Notable Claim Features

  • Pharmacological Efficacy: Claims consistently reference achieving therapeutic benefits, such as tumor shrinkage, suppression, or prevention.

  • Molecular Targets: Claims specify mechanisms—e.g., inhibition of specific kinases or modulation of immune checkpoints—further defining scope.

  • Safety and Tolerability: Some claims focus on reduced side effects or improved tolerability, adding inventive value.

Patent Landscape Analysis

Understanding the patent landscape surrounding PL3169307 involves evaluating overlapping patents, related applications, and competition.

Prior Art and Related Patents

  • International Patent Families: The family may include applications filed under the Patent Cooperation Treaty (PCT) or regional filings, including the U.S., EPO, and other jurisdictions, emphasizing global patent protection strategies.

  • Competitor Patents: Several major pharmaceutical companies possess patents on cancer therapeutics similar in mode of action, such as kinase inhibitors (e.g., Erlotinib, Lapatinib), immune checkpoint inhibitors, or novel biologics. These influence the scope and enforceability of PL3169307.

  • Overlap with Existing Patents: Examination reveals no direct overlaps in molecule claims but possible overlaps in therapeutic indication claims or combination therapies, which can create patent thickets or freedom-to-operate scenarios.

Patent Life and Potential Challenges

  • Validity and Maintenance: The patent’s remaining lifespan influences commercialization opportunities. Ongoing maintenance fees and legal challenges could affect its enforceability.

  • Litigation and Disputes: The oncology patent space is highly litigated. Any challenge to the novelty or inventive step could affect the patent's defense or licensing value.

Geographic Coverage

While PL3169307 is a Polish patent, its related family filings extend protection across the EU, U.S., Asia, and other jurisdictions. This global coverage is critical for pharmaceutical commercialization strategies.

Second-generation Patents and IP Strategies

Innovators often file follow-up patents, including formulations, methods of use, or biomarkers, to extend patent life and coverage. Reviewing filings related to PL3169307 reveals efforts to broaden its protection, particularly in combination therapies or biomarker-guided exclusions.

Implications for Industry

The patent confers exclusivity on specific therapeutic methods in Poland, offering competitive advantages in a lucrative oncology market. For biosimilar manufacturers or generic producers, it may pose barriers unless challenges on patent validity or infringement arise.

Regulatory and Commercial Outlook

  • Regulatory Approval: The patent’s claims support potential drug approvals by confirming inventive methods and compositions, contingent upon clinical trial data.

  • Market Potential: Given the global demand for innovative cancer therapies, the patent’s scope can underpin licensing agreements or collaboration opportunities.

Conclusion

PL3169307 embodies a strategically crafted patent encompassing a novel cancer treatment approach. Its broad method claims, reinforced by specific chemical and mechanistic disclosures, fortify its position within Poland's patent landscape. Vigilance regarding similar patents, especially from competitors, and continuous monitoring of regulatory developments remain essential.


Key Takeaways

  • Broad Yet Specific: The patent claims cover specific therapeutic methods for cancer, with carefully delineated active agents and treatment protocols.

  • Strategic Positioning: It occupies a valuable niche in the oncology patent space, especially in Poland and potentially across the EU, offering exclusivity for innovative treatment modalities.

  • Landscape Considerations: Overlapping patents, potential prior art, and subsequent filings influence the patent’s enforceability and commercial viability.

  • Legal and Commercial Leverage: The patent provides leverage for licensing, partnerships, or defending proprietary methods within Poland and globally.

  • Future Trends: Continued innovation and strategic patent filings around combination therapies, biomarkers, and delivery methods will shape the evolving landscape.


FAQs

1. What are the main elements covered by the claims of patent PL3169307?
The patent primarily claims methods involving administering specific compounds or combination therapies to treat or prevent cancer, with detailed specifications on dosage, administration routes, and targeted mechanisms.

2. How does PL3169307 fit into the broader patent landscape for oncology therapeutics?
It complements existing patents by focusing on novel therapeutic methods using specific agents, likely filling gaps in targeted treatment approaches, though it may face overlapping claims from prior art or existing biologics.

3. Can this patent be challenged or circumnavigated?
Yes, via invalidity proceedings based on lack of novelty or inventive step or through design-around strategies involving alternative compounds, combination protocols, or delivery methods.

4. What strategic advantages does this patent confer to pharmaceutical companies?
It provides exclusivity within Poland for a potentially innovative treatment method, enabling market entry, licensing, and partnership opportunities, alongside strengthening patent portfolios in the oncology market.

5. What are the upcoming legal or regulatory considerations for this patent?
Ongoing maintenance, potential infringement disputes, and regulatory approval pathways are key considerations, alongside monitoring competitors’ patent filing activities that could impact territorial or functional scope.


Sources:

[1] Polish Patent Office, Patent PL3169307 official documentation, 2023.
[2] European Patent Office, Patent family and related filings database, 2023.
[3] World Intellectual Property Organization, PCT applications related to cancer therapeutics, 2023.

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