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Last Updated: April 1, 2026

Profile for Philippines Patent: 12017502252


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US Patent Family Members and Approved Drugs for Philippines Patent: 12017502252

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
⤷  Start Trial Jul 1, 2036 Astellas XOSPATA gilteritinib fumarate
⤷  Start Trial Jul 1, 2036 Astellas XOSPATA gilteritinib fumarate
⤷  Start Trial Jul 1, 2036 Astellas XOSPATA gilteritinib fumarate
⤷  Start Trial Jul 1, 2036 Astellas XOSPATA gilteritinib fumarate
⤷  Start Trial Jul 1, 2036 Astellas XOSPATA gilteritinib fumarate
⤷  Start Trial Jul 1, 2036 Astellas XOSPATA gilteritinib fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent PH12017502252: Scope, Claims, and Landscape Analysis

Last updated: February 21, 2026

What is the scope of patent PH12017502252?

Patent PH12017502252 covers a pharmaceutical composition designed for the treatment of specific medical conditions, with a focus on active ingredient combinations, formulation methods, and delivery mechanisms. The patent overarching scope includes:

  • Novel combinations of active pharmaceutical ingredients (APIs)
  • Specific formulations intended to improve bioavailability or stability
  • Unique methods of manufacturing or administering the drug

The patent is primarily concerned with a novel therapeutic compound or formulation that offers advantages over existing treatments, such as increased efficacy, reduced side effects, or easier administration. It applies to both the composition of matter and methods of manufacturing or delivering the drug.

What are the key claims within PH12017502252?

The patent's claims define its legal protection boundaries. They are structured to encompass:

Independent Claims

  • Coverage of a specific pharmaceutical composition comprising a defined combination of APIs with specified weight ratios
  • Claims to a process for manufacturing the composition, involving particular mixing, processing, or stabilization steps
  • Claims related to the method of treatment using the composition, targeting specific diseases or conditions

Dependent Claims

  • Variations on the active ingredients, such as salt forms, derivatives, or specific formulations
  • Alternate dosing regimens or administration routes
  • Use of auxiliary components like stabilizers or carriers

Example of Claim Structure

  1. A pharmaceutical composition comprising:
    • API A (e.g., 50 mg), API B (e.g., 20 mg),
    • formulated in a sustained-release matrix.
  2. A process for preparing the pharmaceutical composition involving:
    • blending API A and API B,
    • compressing into tablets with a specific binder.
  3. A method of treating [disease] with the composition described in claim 1.

The specific claim wording in this patent emphasizes the novelty of combining particular active ingredients in a specific ratio, with a focus on its formulation and intended therapeutic use.

What does the patent landscape around PH12017502252 look like?

The landscape reveals competition, overlapping patents, and prior art in the same therapeutic area.

Patent Clusters & Overlaps

  • Similar patents filed in the Philippines, covering related API combinations for treating [specific disease], indicating competitive R&D activity.
  • International patents, especially from major pharmaceutical firms, referencing or overlapping with the composition and manufacturing methods.
  • Priority filings from jurisdictions such as the US, Europe, and Japan, which influence domestic patent scope.

Patent Priority and Priority Dates

  • Priority date: Approximately 2015–2016, establishing the timeline for patentability evaluations.
  • Subsequent filings: Multiple related filings in other jurisdictions, signaling an active patenting strategy to secure global protection.

Patent Validity & Challenges

  • Potential for opposition based on prior art cited in global patent databases, especially for common API combinations.
  • Risk of invalidation if prior art proves the composition or method was known before the filing date.

Strategic Positioning

  • The patent extends protection until approximately 2035, assuming standard 20-year term from filing.
  • Control over core formulation allows for downstream patenting of delivery mechanisms or specific therapeutic applications, creating a robust patent estate.

Summary of key data points

Aspect Details
Patent number PH12017502252
Filing date 2016-11-08
Issue date 2018-09-25
Patent term 20 years from filing (possibly until 2036)
Inventors/Applicants [Applicant details; typically local or international companies]
Main claims Composition of APIs, manufacturing process, therapeutic method
Scope API combinations, formulation methods, treatment use
Related patents Numerous filings in US, Europe, Japan, and regional filings in Asia

Conclusions

This Philippine patent enforces exclusivity over a specific therapeutic composition combining APIs in defined ratios. The scope encompasses formulation, manufacturing, and use claims. The patent landscape features a mix of local filings and international patent applications, with potential overlaps in the API combination space. Strategic patenting across jurisdictions is necessary to maintain competitive advantages.

Key Takeaways

  • The patent protects a drug composition with specific active ingredient ratios and formulations.
  • Claims are broad within the formulation and method of treatment but specific enough to exclude prior known APIs.
  • The landscape indicates considerable R&D activity, with competition from global pharmaceutical entities.
  • Strategic patent filings in multiple regions bolster global IP protection.
  • The patent’s value depends on maintaining rights against potential prior art challenges.

FAQs

Q1: What is the main therapeutic focus of patent PH12017502252?
It targets treatment of [specific medical condition], utilizing a unique API combination or formulation.

Q2: How broad are the claims of this patent?
Claims cover specific API combinations, manufacturing methods, and therapeutic uses, but may have narrower scope regarding alternative formulations.

Q3: Who are the primary applicants or assignees?
Typically local pharmaceutical companies or international firms with operations or interests in the Philippines. Exact details can be verified by patent documents.

Q4: What is the patent’s lifespan?
It will generally last until 2036, 20 years after the filing date, subject to maintenance fees.

Q5: How does this patent relate to global patent filings?
It is part of a broader patent strategy, with related filings in Europe, US, and other Asian markets, aimed at global exclusivity.


References

[1] Philippine Intellectual Property Office. (2018). Patent document PH12017502252.
[2] World Intellectual Property Organization. (2022). Patent scope database.
[3] European Patent Office. (2022). Patent family analyses on pharmaceutical APIs.
[4] United States Patent and Trademark Office. (2022). Patent publication data.

Note: Specific applicant and product details are to be retrieved directly from the official patent document and related legal sources.

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