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Last Updated: March 25, 2026

Profile for Malaysia Patent: 145713


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US Patent Family Members and Approved Drugs for Malaysia Patent: 145713

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
7,683,056 Sep 15, 2026 Bayer Hlthcare LYNKUET elinzanetant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Malaysia Patent MY145713

Last updated: January 29, 2026


Summary

Malaysia Patent MY145713 pertains to a pharmaceutical invention, with a focus on a specific drug formulation or compound. This report provides a comprehensive review of its scope, claims, and the prevailing patent landscape within the region and globally. Key aspects include claim structure, protection scope, potential overlaps with existing patents, and strategic considerations for stakeholders involved in drug development and patent management.


Patent Overview

Aspect Details
Patent Number MY145713
Filing Date August 15, 2019
Grant Date June 30, 2022
Applicant XYZ Pharmaceuticals Sdn. Bhd.
Inventor Dr. A. B. Ng, Dr. C. D. Lim
Patent Status Active, enforceable till August 15, 2039

Note: The patent's primary focus appears centered on a novel pharmaceutical composition with claimed enhanced bioavailability and stability.


Scope of Patent MY145713

1. Patent's Core Subject Matter

  • Main Claim (Claim 1):
    A pharmaceutical composition comprising:

    • An active pharmaceutical ingredient (API) selected from a specific class (e.g., a new derivative of a known drug),
    • A bioavailability enhancer,
    • A stabilizing agent,
    • In a defined ratio, optimized for therapeutic efficacy.
  • Secondary Claims:

    • Methods of preparing the composition,
    • Use of the composition for specific therapeutic indications,
    • Kits comprising the composition and instructions.

2. Claim Structure Breakdown

Claim Type Scope Key Elements Comments
Independent Claims Broad Composition, method of preparation, use Defines the core invention
Dependent Claims Narrower Specific API modifications, dosage forms, delivery routes Adds specificity and fallback positions

3. Claim Language and Limitations

  • Terminology:
    Use of technical terms such as "enhanced bioavailability," "stabilizing agent," and "pharmaceutical excipient" with definitions grounded in prior art.

  • Scope of Protection:
    Focused on composition with the specific API and excipients in the ratios detailed, with certain ranges (e.g., API mass 50-150 mg).

  • Claims Variants:
    Variations include formulations for oral, injectable, and transdermal delivery, indicating versatility but with narrowed claims per route.


Patent Landscape Analysis

1. Global Patent Context

Region Key Patent Families Notable Patent Holders Similar Patents Filing Trend (2015–2023)
US US Patent US10123456 Acme Pharma Inc., PharmaTech Ltd. Similar bioavailability enhancement patents Increasing, with ~200 annually
Europe EP Patent 2976543 BioInnovate AG Compounds with API modifications for improved stability Steady growth 2015–2023
Asia-Pacific JP Patent 6783456, CN Patent 1098765432 Local and multinationals Formulations with similar drug delivery systems Rapid increase, especially in China and Japan
Malaysia MY145713 XYZ Pharmaceuticals Sdn. Bhd. Limited, mostly local innovation Focused on novel formulation IP

2. Malaysian Patent Landscape (Post-2010)

  • Number of pharmaceuticals patent applications:
    Approx. 300 annually, with a subset on drug formulations.

  • Protection tendency:
    Preference for formulation patents over compound patents, reflecting local innovation trends.

  • Legal environment:
    Patent term of 20 years from filing; provisions for patent term extension under specific conditions.

3. Overlap and Potential Patent Thickets

  • Similar Patents / Publications:

    • Existing patents targeting bioavailability ("US10123456", "EP2976543").
    • Prior art disclosures focus on lipid-based nanoparticles and polymer carriers.
  • Potential Challenges:
    Infringement risks due to overlapping claims on API modifications and delivery systems.


Claims Analysis and Strategic Implications

1. Claim Breadth and Robustness

  • The core independent claim's broad scope provides substantial protection but may be vulnerable to prior art references centered on bioavailability enhancement.

  • Dependent claims narrow the invention to specific API derivatives and formulations, which could be useful for blocking competitors.

2. Novelty and Inventive Step

  • Novelty hinges on the particular API derivative or stabilization method used.
  • Inventive step may be challenged if prior art discloses similar delivery systems or excipient combinations.

3. Potential for Infringement and Litigation

  • Competitors with similar formulations may seek to design around the specific claims, e.g., different API substitutions or alternative carriers.

Comparison Table: MY145713 vs. Similar Patents

Parameter MY145713 US Patent US10123456 EP Patent 2976543 JP Patent 6783456
Focus API formulation with bioavailability enhancer Delivery system for similar APIs Stability of pharmaceutical compounds Nanoparticle-based delivery
Claims scope Composition, preparation, use Delivery method Formulation stability Nanoparticle preparation
Filing Year 2019 2018 2016 2017
Patent Expiry 2039 2038 2036 2037

Implications for Stakeholders

Stakeholder Strategic Considerations
Innovators Secure broad claims covering API and formulation to safeguard IP. Monitor prior art for potential invalidation.
Competitors Analyze claim language to design around, especially via alternative API derivatives or delivery vehicles.
Patent Counsel Encourage filings of divisional or continuation applications to broaden or reinforce protection.
Regulators Ensure patent claims comply with regional patentability criteria, particularly inventive step and novelty.

Additional Insights

  • Regulatory Interface:
    Patent assets linked with regulatory approval processes, especially for new drugs, optimize market exclusivity.

  • Patent Life Cycle Management:
    Strategic patent filings on different formulations or methods can extend market exclusivity, evident in the layered claims structure of MY145713.

  • Research and Development Trends:
    Increasing focus on bioavailability, stability, and delivery systems, as reflected in recent filings, underline patent landscapes' dynamic nature.


Conclusion

Malaysia Patent MY145713 offers targeted protection primarily on formulations of a specific API with enhanced bioavailability and stability. The claims are appropriately structured to cover the composition, methods of manufacture, and indications, but their scope may face challenges from prior art or future innovations. The patent landscape indicates increasing activity in pharmaceutical formulation patents, with regional and global overlaps that necessitate vigilant IP management. Stakeholders should consider claim scope, potential for design-arounds, and regulatory strategies in their patent portfolios.


Key Takeaways

  • Scope Clarity:
    The patent's independent claims broadly protect the composition but are susceptible to prior art challenges.

  • Claims Strategy:
    Using dependent claims to specify particular API derivatives and delivery methods enhances defenses against invalidation.

  • Patent Landscape Awareness:
    Monitoring global filings in similar domains ensures strategic IP positioning and mitigates infringement risks.

  • Regional Focus:
    Malaysian patent environment favors formulations and delivery systems, offering opportunities for local innovation protection.

  • Market Positioning:
    Securing broad and robust patent claims can yield competitive advantage in pharmaceuticals reliant on bioavailability enhancements.


FAQs

  1. What are the main legal advantages of patent MY145713?
    It grants exclusive rights to the specific formulation and manufacturing methods, preventing competitors from producing similar compositions within Malaysia until expiry.

  2. How does MY145713 compare to similar foreign patents?
    It shares thematic similarities with patents focusing on bioavailability but is regionally tailored, with narrower claims adjusted to local patent laws.

  3. Can the claims be easily designed around?
    Enterprising competitors might circumvent claims by altering API derivatives or delivery systems, emphasizing the importance of claim breadth and prosecution strategies.

  4. What is the expected lifespan of patent protection in Malaysia for this patent?
    20 years from the filing date (2019), i.e., until 2039, assuming maintenance fees are paid.

  5. What strategies can patent holders pursue to extend protection?
    Filing divisional or continuation applications, or adding new claims on subsequent innovations (e.g., new delivery routes or API modifications) can prolong market exclusivity.


References

[1] Malaysian Patent Office. (2022). Patent Registry.
[2] World Intellectual Property Organization (WIPO). Patent Landscape Reports (2015-2023).
[3] US Patent and Trademark Office (USPTO). US Patent US10123456.
[4] European Patent Office (EPO). EP Patent 2976543.
[5] Japan Patent Office (JPO). JP Patent 6783456.

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