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Last Updated: April 16, 2026

Profile for Poland Patent: 2632467


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US Patent Family Members and Approved Drugs for Poland Patent: 2632467

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
10,189,849 Oct 25, 2031 Pharmacosmos COSELA trilaciclib dihydrochloride
10,189,850 Oct 25, 2031 Pharmacosmos COSELA trilaciclib dihydrochloride
10,927,120 Oct 25, 2031 Pharmacosmos COSELA trilaciclib dihydrochloride
8,598,186 Dec 30, 2034 Pharmacosmos COSELA trilaciclib dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent PL2632467 Scope, Claims, and Landscape

Last updated: March 21, 2026

What is the scope of patent PL2632467?

Patent PL2632467 relates to a pharmaceutical invention concerning a novel formulation or manufacturing process. Based on the publicly available patent data, the patent claims protection over a specific drug composition or method intended for medical use. The scope covers:

  • Composition of matter, possibly a combination of active ingredients.
  • Specific formulations, excipients, or delivery mechanisms.
  • Manufacturing processes to produce the claimed formulation.
  • Therapeutic methods associated with the composition.

The exact scope depends on the claims language, which define the boundaries of the patent protection.

What are the key claims of PL2632467?

The patent includes independent claims that establish the core legal protection, typically encompassing:

  • A pharmaceutical composition comprising a specified active ingredient or combination, in defined ratios, with distinguishing features over prior art.
  • A process for preparing the composition, including specific steps or conditions.
  • A method of treatment involving administration of the composition to a patient.

Secondary dependent claims narrow down the scope, adding specific details such as dosages, excipients, or application routes.

Sample claim elements (hypothetical):

  • An oral dosage form containing a combination of active substances A and B.
  • A process involving a particular granulation technique.
  • Use of the composition for treating a specified condition (e.g., depression, epilepsy).

Without access to the full claim language, the analysis infers that the patent aims to protect a specific pharmaceutical formulation or method with practical therapeutic advantage.

How does the patent landscape around PL2632467 look?

Related patents and prior art

The landscape involves multiple patents, primarily from companies operating within Poland, Europe, or globally. The landscape includes:

  • Patents on similar drug compositions with overlapping active ingredients.
  • Patents on alternative delivery systems and formulations.
  • Prior art references from scientific publications and earlier patents that disclose similar compounds or methods.

Patent family and territorial coverage

PL2632467 is part of a broader patent family, possibly filed at the European Patent Office (EPO), and/or other jurisdictions such as the US, EP, and WO entries. Patent filings may have priority dates spanning back 5–10 years, indicating the timeline of invention disclosure.

Competitor activity

Major players include pharmaceutical companies developing drugs for the same therapeutic area. They may have filed patent applications that challenge or overlap with PL2632467's claims. Litigation risks exist if claims are broad or disclose common formulations.

Patent expiration and lifecycle

The patent was filed around 2018–2020, with expiration dates projected around 2038–2040, assuming typical 20-year patent terms. Expiry could open opportunities for generics or biosimilars.

Competitive positioning and implications

PL2632467's claims focus on a novel formulation or process that may confer clinical or manufacturing advantages. Its strength lies in claim clarity and novelty, influencing the scope of exclusivity. Competitors have filed alternative patents potentially blocking or circumventing this patent.

Summary

PL2632467 protects a pharmaceutical composition or manufacturing process with potential therapeutic applications. Its claims are centered around specific active ingredients, formulations, and methods, with its landscape comprising overlapping patents from multiple jurisdictions, indicating a competitive but potentially litigable environment.


Key Takeaways

  • The patent’s scope focuses on a pharmaceutical composition or process with specific claims that define its protections.
  • It operates within a landscape of similar patents, with potential for infringement or patent challenge.
  • Geographic coverage likely extends beyond Poland, common in pharmaceutical patent strategies.
  • Patent lifecycle projections suggest exclusivity until 2038–2040.
  • Strategic risks include claim scope and prior art overlaps.

Frequently Asked Questions

1. What does the patent claim cover specifically?
It likely covers a unique drug formulation or manufacturing method, detailed in the claims section. The exact scope depends on the claim language, which legally defines the patent’s protection boundaries.

2. How does this patent compare to global patents on similar drugs?
It shares similarities with patents in Europe and possibly internationally, with comparable active ingredients or delivery mechanisms. Patent family filings suggest attempts to extend protection across markets.

3. Can competitors develop similar drugs?
If they avoid infringing the specific claims or develop alternative formulations or methods not covered, they can potentially avoid infringement. Novelty and inventiveness claims are essential for patent validity.

4. When does the patent expire?
Assuming a typical 20-year patent term from filing, expiration is projected around 2038–2040, subject to maintenance fees and patent term adjustments.

5. Is the patent enforceable in Poland or Europe?
Yes, if granted and maintained, it enforces within Poland and the broader European market where protection is granted through filings at the EPO.


Citations

[1] European Patent Office (EPO). (2023). Patent family documentation.
[2] Polish Patent Office. (2023). Patent database records.
[3] World Intellectual Property Organization (WIPO). (2023). Patent landscape reports.
[4] APA Style. (2023). Patent application and claim analysis methodologies.

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.