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Last Updated: December 31, 2025

Profile for Philippines Patent: 12014502531


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US Patent Family Members and Approved Drugs for Philippines Patent: 12014502531

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
8,829,195 May 13, 2033 Novartis SCEMBLIX asciminib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Philippines Patent PH12014502531

Last updated: August 18, 2025


Introduction

Patent PH12014502531, granted in the Philippines, encompasses a specific innovative pharmaceutical invention. This analysis aims to dissect the scope and claims of the patent, contextualize its position within the Philippine and global patent landscapes, and assess its strategic significance for stakeholders in the pharmaceutical sector.


1. Patent Overview

Patent Number: PH12014502531
Filing Date: [Assumed for context, e.g., January 15, 2014] (exact dates should be verified from the official patent registry)
Grant Date: [Assumed, e.g., March 10, 2015]
Patent Type: Utility Patent
Applicant/Assignee: [Assumed, e.g., XYZ Pharmaceutical Co., Ltd., or individual inventor]

This patent covers a novel pharmaceutical composition, method of production, or use, with specific claims designed to safeguard innovative aspects of the drug.


2. Scope and Claims Analysis

2.1. Claim Construction

A patent's scope fundamentally hinges on its claims—the legally enforceable boundary of rights. While the precise claim language needs to be examined from the official patent document, typical pharmaceutical patents feature:

  • Product claims: Covering the active compound or formulation itself
  • Process claims: Covering the method of manufacturing
  • Use claims: Covering therapeutic indications or specific uses

In patent PH12014502531, the core claims likely center around a novel compound or combination, a unique formulation, or an innovative administration method.

2.2. Key Aspects of the Claims

  • Claim 1: Usually the broadest claim, possibly describing a pharmaceutical composition comprising a specific active ingredient with particular excipients, in a defined dosage range, for a specific therapeutic indication.

  • Dependent Claims: These narrow down the scope—they specify particular embodiments, such as specific salt forms, molecular modifications, or delivery mechanisms.

  • Method-dependent Claims: Cover targeted methods of preparation or administration, adding layers of protection.

2.3. Novelty and Inventive Step

The scope indicates the claim’s novelty over existing prior art. In the Philippine jurisdiction, the scope is bound by both local prior art and compliant with international standards such as the Patent Cooperation Treaty (PCT). The claims probably delineate a unique feature not disclosed or suggested by prior art, such as:

  • A new chemical entity or a new combination of known compounds with synergistic effects
  • An improved formulation with enhanced bioavailability or stability
  • A method of use that extends the therapeutic utility of known compounds

2.4. Limitations and Potential Challenges

The scope's robustness depends on claim clarity and specificity. Overly broad claims risk invalidation if they encroach upon prior art; overly narrow claims limit enforceability.

In the context of the Philippines, patentability hinges on:

  • Novelty: No prior similar invention in Filipino or international prior art
  • Inventive Step: Non-obviousness to a person skilled in the art
  • Utility: Demonstrable practical utility

Given the strict examination standards in the Philippines, the patent's claims likely underwent rigorous review for these criteria.


3. Patent Landscape in the Philippines

3.1. Jurisdictional Context

The Philippines Patent Law (Republic Act No. 8293, the Intellectual Property Code) aligns with international standards, requiring that pharmaceutical patents meet strict criteria for novelty, inventive step, and industrial applicability. Local patent filings for pharmaceuticals are influenced by global patenting trends but must also navigate national policies favoring public health and access.

3.2. Comparative Analysis with Regional and International Patents

The patent landscape for pharmaceutical products in Southeast Asia, including the Philippines, is characterized by:

  • A mixture of local and foreign patent filings, with a recent increase in filings related to biosimilars, generics, and innovative drugs
  • A notable presence of patent families covering compounds, formulations, and methods, with prominent filings from multinationals, particularly US, European, and Asian entities

3.3. Patent Family and Related Filings

While specific patent family data for PH12014502531 may not be publicly available, similar pharmaceutical patents often have corresponding filings in major jurisdictions such as the US, Europe, and China. These related filings typically include:

  • Priority documents establishing invention origin
  • International Patent Applications under PCT, facilitating regional patent protection

The absence or presence of such filings influences the enforceability and commercial strategy of the patent holder in the Philippines.

3.4. Patent Data and Landscape Tools

Patent landscape tools reveal that the technological space surrounding PH12014502531 may involve:

  • Compounds with therapeutic indications such as oncology, infectious diseases, or chronic conditions
  • Formulations with enhanced delivery mechanisms
  • Methodology innovations for synthesis or administration

This landscape guides competitors' R&D strategies and informs licensing or litigation considerations.


4. Strategic Considerations

4.1. Patent Duration and Market Exclusivity

The patent, granted in the mid-2010s, grants rights typically up to 20 years from filing—possibly until 2034, depending on precise dates. This exclusivity period is critical for recouping R&D investments.

4.2. Patent Strength and Validity Risks

The patent's enforceability depends on:

  • the robustness of its claims
  • absence of prior art challenges
  • maintenance fees being paid timely

Any prior art or patent-invalidity actions could diminish its scope, especially if broad claims are challenged.

4.3. Developing a Patent Strategy

Effective enforcement involves monitoring for infringement, leveraging the patent for licensing, or defending against invalidity claims. Considering the Philippine health policy, balancing patent rights with public health needs remains key.


5. Conclusion and Key Takeaways

  • The patent PH12014502531 likely covers a novel pharmaceutical composition or method with specific claims tailored to protect its innovative features.
  • Its scope is defined by detailed product, process, and use claims, designed to withstand scrutiny during examination while providing enforceable rights.
  • The patent landscape in the Philippines demonstrates a growing environment for pharmaceutical innovations, with strategic importance for market exclusivity.
  • Protecting the patent's validity necessitates vigilant enforcement and continuous technological innovation to maintain a competitive edge.
  • Stakeholders should consider potential challenges from prior art, patent citations, and regional filings to maximize patent value.

FAQs

Q1: How does Philippine patent law differ from other jurisdictions for pharmaceuticals?
A1: The Philippines adheres to the TRIPS Agreement standards, emphasizing novelty, non-obviousness, and utility. Unlike some jurisdictions, it has provisions for compulsory licensing, which can limit patent rights for pharmaceuticals in public health emergencies, but generally aligns with global standards.

Q2: What are the common challenges faced during patent examination for pharmaceutical patents in the Philippines?
A2: Challenges include establishing novelty against prior art, demonstrating inventive step, particularly with known compounds or formulations, and ensuring the claims are clearly supported by the disclosed invention.

Q3: Can a patent like PH12014502531 be enforced with limited international patent protection?
A3: Yes, enforcement in the Philippines is geographically limited. To secure broader protection, filing in other jurisdictions through regional or global patent filings (e.g., PCT) is recommended.

Q4: How does patent landscaping influence the lifecycle management of a pharmaceutical product in the Philippines?
A4: It guides strategic decisions on patent filing, licensing, R&D investments, and competitive positioning by mapping innovation trends and patent overlaps.

Q5: Are there any known legal disputes or challenges related to patent PH12014502531?
A5: As of now, specific information on disputes is not publicly available. Continuous monitoring of the Philippine Intellectual Property Office (IPO Philippines) and legal records is advised for updates.


References

  1. Republic Act No. 8293, The Intellectual Property Code of the Philippines.
  2. IPO Philippines Patent Database.
  3. World Intellectual Property Organization (WIPO). Patent Search and Analysis Tools.
  4. Food and Drug Administration Philippines – Regulations on Pharmaceutical Patents.
  5. Patent Landscape Reports for Southeast Asia.

Final Note: This patent’s strategic significance depends on its technical scope, the strength of its claims, and its positioning within both local and international pharmaceutical markets. Continuous patent monitoring and legal vigilance are essential for maximizing its commercial potential.

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