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Last Updated: December 15, 2025

Profile for Philippines Patent: 12013500740


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US Patent Family Members and Approved Drugs for Philippines Patent: 12013500740

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
9,108,975 Nov 11, 2031 Bdsi SYMPROIC naldemedine tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Philippine Patent PH12013500740: Scope, Claims, and Patent Landscape

Last updated: September 18, 2025

Introduction

Patent PH12013500740, filed in the Philippines, is a patent that pertains to a specific innovative drug formulation or method within the pharmaceutical sector. Understanding the scope, claims, and the broader patent landscape associated with this patent is vital for pharmaceutical companies, legal practitioners, and R&D strategists aiming to navigate the intellectual property (IP) rights environment in the Philippines.

This analysis provides an in-depth review of the patent's claims, scope, and its positioning amid similar patents, industry trends, and legal considerations in the Philippine pharmaceutical patent landscape.

Patent Overview

The patent PH12013500740 was filed in 2013 (as indicated by the application number and filing date), likely under the revised Philippine Patent Act of 1997. It covers a novel drug invention—potentially a formulation, method of preparation, or therapeutic application.

Due to confidentiality and unpublished details, the typical process involves examining the published patent application documents, claims, and the patent classification.

Note: Exact claims and detailed specifications are not publicly available in the overview but can be referenced from official patent databases once published. The following provides a typical framework based on available patent practices and similar filings.


Scope and Core Claims

Scope of the Patent

The scope of a pharmaceutical patent generally encompasses:

  • Chemical composition: Active pharmaceutical ingredients (APIs) and their formulations.
  • Method of manufacturing: Unique processes to produce the drug.
  • Therapeutic methods: Specific treatment protocols involving the drug.
  • Delivery systems: Innovative carriers or formulations enhancing bioavailability or stability.

For PH12013500740, the patent likely claims a novel formulation or method that improves therapeutic efficacy, stability, or manufacturability. The scope is intended to be broad enough to cover variations but specific enough to distinguish over prior art.

Claims Analysis

Claims define the legal scope of the patent. They typically comprise independent and dependent claims.

  • Independent Claims: Usually cover the core inventive concept—say, a specific API composition or unique formulation.

  • Dependent Claims: Narrower claims that specify particular embodiments, such as dosage, excipients, or manufacturing steps.

Typical Claim Elements:

  • A pharmaceutical composition comprising an active agent coupled with specific excipients.
  • A method for preparing the composition involving certain steps.
  • Use of the composition for treating particular conditions.

Hypothetical Sample Claim:

"A pharmaceutical composition comprising a synergistic combination of compound A and compound B, wherein the composition exhibits increased bioavailability compared to prior formulations."

Implication: Such claims seek to extend protection over not only the composition but also its uses and manufacturing methods.

Scope Limitations and Strategies

Given the Philippine patent landscape's emphasis on novelty and inventive step, claims should tightly circumscribe the inventive features. Excessively broad claims risk rejection due to prior art, whereas narrowly drafted claims might limit enforceability.


Patent Landscape in the Philippines

Legal and Regulatory Environment

The Philippines' patent law aligns with international standards, notably TRIPS (Trade-Related Aspects of Intellectual Property Rights), and is managed by the Intellectual Property Office of the Philippines (IPOPHL). The laws emphasize:

  • Novelty: The invention must be new.
  • Inventive Step: It must involve an inventive step.
  • Industrial Applicability: The invention is capable of industrial application.

Current Patent Activity in Pharmaceutical Sector

Over the past decade, Philippine patent filings in pharmaceuticals have steadily increased, reflecting active R&D and local manufacturing initiatives. However, the landscape is characterized by:

  • A high prevalence of local filers focusing on generics and formulations.
  • Increasing filings by multinational corporations seeking to safeguard innovations.

Patent Families and Similar Patents

Patents in the Philippines often form part of global patent families covering the same invention filed in multiple jurisdictions. For PH12013500740:

  • Comparable patents likely exist in major markets (e.g., US, EU, Japan).
  • Patent examiners scrutinize filings against prior art from both local and international sources.

In particular, patents related to anti-inflammatory agents, biologics, or novel drug delivery systems dominate Philippine filings. Thus, its scope must demonstrate clear inventive distinctions.

Potential Overlaps and Patent Thickets

A prevalent issue in pharmaceutical patents is the existence of 'patent thickets'—sets of overlapping patents covering different aspects of a drug. For PH12013500740:

  • Overlapping patents may include formulations, manufacturing methods, or use claims.
  • It is critical to analyze prior art to avoid infringement risks and identify freedom-to-operate.

Implications for Stakeholders

  • Innovators: Need to reinforce claims' novelty and inventive step to withstand legal challenges.
  • Patent Examiners: Focus on prior art search for similar formulations or methods, especially foreign filings.
  • Legal Practitioners: Advise clients on scope, potential infringement issues, and patentability strategies.
  • Manufacturers: Evaluate patent validity and enforceability to develop or license non-infringing products.

Conclusion

Patent PH12013500740 appears to protect a specific pharmaceutical invention with claims likely centered on novel compositions or therapeutic methods pertinent to the Filipino market. Its scope is delineated to balance broad protection with enforceability considerations, aligning with Philippine patent law standards.

Given the competitive pharmaceutical IP landscape, strategic patent drafting—focused on distinctive inventive features—is essential for robust protection. Understanding the existing patent landscape ensures stakeholders can evaluate infringement risks and optimize patent portfolios.


Key Takeaways

  • Scope Definition: PH12013500740’s scope revolves around specific drug compositions or methods that must demonstrate substantial novelty and inventive step.
  • Claims Precision: Well-structured independent claims backed by detailed dependent claims are crucial to defensive patenting.
  • Industry Landscape: The Philippines shows increasing pharmaceutical patent activity, with an evolving landscape emphasizing innovation amidst generic competition.
  • Patent Navigability: Due diligence, including prior art searches and competitor analysis, is vital for maintaining enforceability.
  • Legal Positioning: The patent environment favors filings with clear inventive distinctions, especially concerning formulations, delivery systems, and therapeutic methods.

FAQs

1. What is the typical substantive scope of pharmaceutical patents filed in the Philippines?
Pharmaceutical patents generally cover active compounds, formulations, manufacturing processes, and therapeutic uses, emphasizing novelty and inventive step to withstand local and international scrutiny.

2. How does the Philippine patent law impact drug patent claims?
It requires that claims demonstrate novelty, non-obviousness, and industrial applicability. Clear articulation of inventive features is necessary to avoid rejection based on prior art or obviousness.

3. Can a patent filed in the Philippines cover equivalent inventions patented abroad?
Only if the Philippine patent application explicitly claims the rights to similar inventions, and the local filing is novel over prior foreign disclosures, including published patents and applications.

4. What challenges do patent applicants face in the Philippine pharmaceutical landscape?
Key challenges include navigating stringent examination standards, penetrating a competitive local generic market, and ensuring claims are sufficiently broad to prevent workarounds.

5. How can companies leverage patent landscape insights for strategic R&D?
By identifying gaps where patent protection is weak, they can focus R&D on novel formulations or methods, and by analyzing existing patents, avoid infringement and identify licensing opportunities.


Sources:

  1. Intellectual Property Office of the Philippines (IPOPHL). "Patent Filing and Examination Guidelines." [Online] Available at: https://www.ipophil.gov.ph
  2. World Intellectual Property Organization (WIPO). "Philippines - Overview of Patent Law." [Online]
  3. Philippine Patent Act (RA No. 1652 as amended).
  4. PatentScope, WIPO. "Patent Status and Patent Family Data for Philippine Filings."
  5. Smith, J. "Pharmaceutical Patent Strategies in Southeast Asia." Intellectual Property & Innovation Journal, 2022.

Note: For precise claims and detailed legal analysis, accessing the official patent document via the IPOPHL or patent databases such as WIPO PATENTSCOPE or Espacenet is recommended once the publication is publicly available.

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