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Last Updated: December 14, 2025

Profile for Malaysia Patent: 197630


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US Patent Family Members and Approved Drugs for Malaysia Patent: 197630

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 Mar 6, 2039 Axsome Malta SUNOSI solriamfetol hydrochloride
⤷  Get Started Free Nov 1, 2038 Axsome Malta SUNOSI solriamfetol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Malaysia Patent MY197630

Last updated: September 11, 2025


Introduction

Malaysia Patent MY197630 pertains to an innovative pharmaceutical invention entered into the Malaysian Intellectual Property Office (MyIPO). Understanding the scope, claims, and landscape surrounding this patent is pivotal for stakeholders involved in drug development, licensing, or IP strategy, especially in Southeast Asia's dynamic pharmaceutical market. This analysis aims to dissect the patent’s claims, explore its legal scope, and contextualize its position within the wider patent environment.


Patent Overview

Patent Number: MY197630
Filing Date: [Insert Filing Date]
Grant Date: [Insert Grant Date]
Ownership: [Insert Assignee/Applicant Name]
Title: [Insert Patent Title] (assumed based on standard nomenclature)

Note: Precise details such as filing/grant dates and ownership would typically be retrieved from MyIPO databases, but in this context, we proceed with generic analysis.[1]


Scope of the Patent

The scope of MY197630 hinges on its detailed claims, which delineate the boundaries of the invention’s legal protection. In pharmaceutical patents, scope primarily considers novel compounds, formulations, methods of use, or manufacturing processes.

Claims Analysis

While the specific wording of the claims is not provided here, typical drug patents encompass:

  1. Compound Claims: Covering the chemical entity itself. Likely includes a core molecule with specific structural features.
  2. Use Claims: Covering therapeutic applications, e.g., treatment of specific diseases.
  3. Formulation Claims: Covering specific compositions or delivery mechanisms.
  4. Process Claims: Methods of synthesizing or manufacturing the compound.

Assumed Focus of MY197630:
Given standard patent practices, MY197630 probably claims a novel chemical compound or a specific therapeutic use scenario with particular structural features or formulations. For example:

  • Compound Claims: “A chemical compound of formula I, characterized by [specific structural features], capable of [specific therapeutic effect].”
  • Use Claims: “Use of the compound for treating [disease or condition], such as [disease].”
  • Method Claims: “A method for synthesizing the compound involving [specific process steps].”

Claim Scope Considerations:
The scope's breadth is critical. Broad claims covering the compound with minimal limitations offer wider protection but face higher invalidity risks if prior art exists. Narrow claims targeting specific derivatives or formulations are easier to defend but limit the scope.


Legal and Patent Landscape Context

Patentability Components

  1. Novelty:
    The compound or invention must be new compared to prior art. In Malaysia, prior art includes international publications, existing patents, and granted Malaysian patents.

  2. Inventive Step:
    The invention must demonstrate an inventive step over existing technologies, considering the prior art landscape. Given Malaysia’s active pharmaceutical patent filings, especially from major players like China, India, and Western firms, inventiveness is evaluated carefully.

  3. Industrial Applicability:
    The patent must be capable of industrial application, which is straightforward for drug compounds and formulations.

Position within the Malaysia Patent Landscape

Malaysia’s patent system aligns with the TRIPS agreement, requiring strict standards for patentability.[2] The country has an active patent scene for pharmaceuticals, with particular emphasis on:

  • Chemical and pharmaceutical innovations from local universities and foreign multinationals.
  • Patent proliferation in areas such as cancer therapeutics, antivirals, and biologics.

The landscape shows heightened patenting activity around compound classes like kinase inhibitors, monoclonal antibodies, and novel drug delivery systems.

Patent Families and Overlap:
Patent MY197630 exists within a broader patent family (assuming based on patent behavior), potentially linked to patents filed in regional or PCT applications. Overlaps with patents in China, India, or the US may exist, especially on core compounds.


Potential Challenges and Opportunities

  • Clarity of Claims:
    Given Malaysia’s scrutiny over claim ambiguity, overly broad claims risk invalidation or infringement fine points.[3] Precise claims emphasizing unique structural aspects or uses are advantageous.

  • Patent Term and Life Cycle:
    The patent’s term—typically 20 years from the filing date—dictates market exclusivity. Monitoring potential extensions or supplementary protections (e.g., pediatric extensions) is essential.

  • Infringement Risks in the Region:
    Given Malaysia’s manufacturing hub status and proximity to regional markets, patent MY197630’s scope impacts not just Malaysia but also regional manufacturing and import activities.


Related Patent Landscape Elements

  1. Competing Patents:
    Other filings in Malaysia or neighboring jurisdictions may challenge or complement MY197630’s claims.

  2. Patent Litigation and Challenges:
    While Malaysia has a relatively nascent patent enforcement environment compared to Western jurisdictions, disputes over drugs, especially generic entries, are emerging.

  3. Regulatory Interface:
    Patent protection complements Malaysian Medicines Authority (MMA) approval processes. Patent status influences market entry timing for generics or biosimilars.


Conclusion

Patent MY197630 appears to secure exclusive rights over a specific pharmaceutical compound or formulation, with claims likely focused on the chemical structure, therapeutic use, or manufacturing method. Its scope is essential in defining the protection boundaries, impacting licensing, commercialization, and potential litigation strategies within Malaysia and the broader Southeast Asian pharmaceutical landscape.

Understanding the patent’s claims and positioning within existing patent families informs innovation strategies, ensuring robust IP protection and competitive advantage while navigating Malaysia’s evolving patent environment.


Key Takeaways

  • Scope Definition: Clear, specific claims centered on novel structural features offer stronger protection, whereas broader claims require meticulous drafting to withstand validity challenges.
  • Patent Landscape Position: MY197630 operates amidst a competitive environment with active filings from international and local entities; monitoring related patents is crucial.
  • Strategic Implication: Effective IP management for this patent involves regular landscape analysis, considering potential overlapping patents and enforcement opportunities.
  • Legal and Market Readiness: Ensure compliance with local patent regulations and align patent strategies with Malaysia’s approval processes for maximized commercial benefits.
  • Regional Considerations: Patent rights in Malaysia form a basis for broader regional patent strategies in ASEAN markets, facilitating potential expansion or licensing.

FAQs

1. What types of claims are typically found in Malaysian drug patents like MY197630?
Malaysian drug patents usually contain compound claims (covering chemical entities), use claims (therapeutic applications), formulation claims (drug delivery systems), and process claims (manufacturing methods).

2. How does Malaysia’s patent environment impact pharmaceutical patent strategy?
Malaysia’s patent system adheres to TRIPS, demanding novelty, inventive step, and industrial applicability. Its enforcement track record influences decisions on patent filing, challenge, and licensing.

3. Can patent MY197630 be challenged or invalidated?
Yes. Through designated legal proceedings, such as opposition or invalidity actions, prior art can be cited to challenge the patent’s validity, particularly if claims are overly broad or lack novelty.

4. How does the patent landscape influence generic drug entry in Malaysia?
Patent protection delays generic entry; infringement or non-infringement determinations shape market dynamics and pricing, especially as patents nearing expiry open opportunities for generics.

5. Are regional patent filings aligned with MY197630?
Likely. Patent families often extend protection through regional or international applications (e.g., PCT), impacting competition and licensing opportunities across ASEAN.


References

[1] MyIPO official database – Patent information.
[2] TRIPS Agreement – World Trade Organization.
[3] Malaysian Patents Act 1983 (amended).

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