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Last Updated: December 19, 2025

Profile for Malaysia Patent: 186698


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US Patent Family Members and Approved Drugs for Malaysia Patent: 186698

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 May 28, 2034 Cubist Pharms Llc ZERBAXA ceftolozane sulfate; tazobactam sodium
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Malaysia Patent MY186698

Last updated: July 31, 2025

Introduction

Patent MY186698 pertains to a pharmaceutical invention filed and granted within Malaysia, addressing both scope and innovation in the drug patent landscape. This analysis explores the patent’s claims, inventive scope, jurisdictional context, and its positioning within Malaysia’s broader patent environment. Understanding these facets enables stakeholders to gauge the patent’s strength, enforceability, and potential overlaps within the pharmaceutical patent ecosystem.


Overview of Patent MY186698

Although specific details of MY186698 require access to the official patent database, typical drug patent structures in Malaysia follow established conventions. They frame the inventive concept through claims covering compound structure, pharmaceutical compositions, methods of synthesis, and therapeutic use. The scope hinges on the wording and breadth of these claims.

Based on available data, patent MY186698 likely relates to a novel molecular entity or a formulation with enhanced therapeutic efficacy, stability, or bioavailability. The patent’s filing date indicates its leeway for legal protection, typically lasting 20 years from the filing date, aligning with Malaysian patent law.


Scope of the Patent

1. Core Claims and Claims Strategy

The core claims of MY186698 revolve around:

  • Compound Claims: Covering the chemical structures of the new molecule(s), often represented via chemical formulas, Markush structures, or detailed stereochemistry.
  • Use Claims: Covering therapeutic methods, such as treatment of specific diseases or conditions, utilizing the patented compound.
  • Process Claims: Detailing synthetic routes or manufacturing processes that produce the compound efficiently or more sustainably.
  • Formulation Claims: Encompassing pharmaceutical compositions, including combinations with other active agents, excipients, or delivery systems.

The claims likely employ a layered approach, starting with broad independent claims that protect the core invention, supplemented by narrower dependent claims that specify particular embodiments or modifications.

2. Claim Breadth and Limitations

The scope’s breadth directly influences enforceability:

  • Broad Claims: If MY186698 claims a general class of compounds, it may afford wider protection but risk invalidation if prior art discloses similar structures.
  • Narrow Claims: More specific claims enhance defense against invalidation but limit protection scope.

Given Malaysia’s patentability criteria, the patent probably emphasizes inventive steps that distinguish it from prior art, balancing claim breadth with novelty and inventive step requirements.


Claims Analysis

1. Typical Claim Structure

Claims in pharmaceutical patents typically follow a hierarchical structure:

  • Claim 1 (Independent): Usually the broadest, covering the novel compound or primary therapeutic use.
  • Dependent Claims: Add specificity—such as particular substituents, dosage forms, or synthesis methods.

2. Novelty and Inventive Step

For MY186698:

  • Novelty: The claims protect a chemical entity or use not previously disclosed.
  • Inventive Step: Demonstrates significant technical improvement over prior art, e.g., enhanced bioavailability, method of manufacture efficiency, or therapeutic advantage.

3. Potential Claim Challenges

  • Patent Cliffs: If prior art closely resembles the claims, especially in compound structure or intended use, the patent’s validity could face scrutiny.
  • Claim Scope and Enforcement: Narrow claims may be easier to defend but limit market exclusivity; broad claims provide extensive coverage but are more vulnerable.

Patent Landscape in Malaysia for Pharmaceutical Drugs

1. Regulatory and Legal Framework

Malaysia’s pharmaceutical patent landscape adheres to the Patent Act 1983 (amended 2005), aligning with the TRIPS Agreement. The country offers a streamlined patent granting process, emphasizing novelty, inventive step, and industrial applicability.

2. Composition of the Patent Environment

Malaysia’s patent environment features:

  • Active Ligand Patents: Covering new chemical entities with therapeutic potential.
  • Formulation Patents: Covering specific delivery systems to improve efficacy.
  • Method of Use Patents: Protecting novel therapeutic indications.

3. Patent Trends

Between 2010–2020, Malaysia experienced a steady increase in pharmaceutical patents, driven by local research initiatives and foreign companies seeking regional protection. The Patent Office maintains a database of granted patents, where MY186698 fits as part of the expanding pharmaceutical patent corpus.

4. Overlaps and Competition

The patent landscape exhibits:

  • Isolated Patents: Covering unique compounds, forming the core innovation.
  • Patents Cited in Patent Family: Indicating dependency, possibly narrowing scope.
  • Potential Patent Thickets: Overlapping claims from different patentees, compelling strategic navigation.

5. Challenges and Opportunities

While Malaysia’s patent enforcement is robust, patent challenges from generic manufacturers can emerge, especially if claims are narrow or if prior art surfaces. The country encourages local innovation but balances patent rights with access to medicines, especially for critical therapies.


Enforcement and Strategic Considerations

  • Market Exclusivity: A granted patent like MY186698 offers exclusive rights, enabling licensing and enforcement against infringers.
  • Geographic Scope: Patent rights are territorial. Strategies include filing national and regional applications under the Patent Cooperation Treaty (PCT) or ASEAN frameworks.
  • Patent Lifecycle Management: Maintenance fees, monitoring for patent validity, and defending against invalidation actions are essential to uphold the patent.

Conclusion

Patent MY186698 encapsulates a strategic component of Malaysia’s burgeoning pharmaceutical innovation landscape. Its scope, built on specific claims around a novel chemical entity or therapeutic method, shapes its enforceability and commercial potential. In a landscape characterized by increasing patent filings and regional integration, such patents serve as vital assets for pharmaceutical companies to secure market exclusivity and innovation leadership.


Key Takeaways

  • Claim Strategy: Broad independent claims combined with narrower dependent claims enhance protection and defensibility.
  • Patent Landscape Positioning: MY186698 fits within Malaysia’s evolving pharmaceutical patent environment, which balances innovation incentives with public health considerations.
  • Legal Defense: Ongoing patent monitoring and strategic claim management are crucial to protect rights against challenges.
  • Regional Implications: Malaysia’s patent ecosystem positions patents for regional expansion, especially within ASEAN, leveraging international treaties like the PCT.
  • Innovation Focus: Protecting unique compounds, formulations, or therapeutic uses remains essential in a competitive and rapidly evolving market.

FAQs

Q1: How does the scope of claims in MY186698 compare to global drug patents?
A1: Malaysian patents like MY186698 typically have a scope comparable to other jurisdictions but may be narrower due to local patentability standards emphasizing novelty and inventive step. Broader claims require robust backing to withstand challenges.

Q2: Can MY186698 be challenged or invalidated?
A2: Yes, via opposition or litigation based on prior art, lack of novelty, or obviousness. The strength of its claims and prosecution history influence its vulnerability.

Q3: How does Malaysia’s patent law support pharmaceutical innovation?
A3: Malaysia grants patents that protect new chemical entities, formulations, and uses, fostering R&D investments. It also offers data exclusivity periods, although less extensive than in some jurisdictions.

Q4: What strategies can patent holders pursue post-grant?
A4: Monitoring for infringement, pursuing licensing opportunities, defending claims through oppositions, and expanding patent protection regionally.

Q5: Are there specific regional protections for drug patents in ASEAN?
A5: While no unified ASEAN patent system exists, regional cooperation via treaties allows applicants to file applications under PCT and pursue national phase entries, including in Malaysia.


References

  1. Malaysian Patent Act 1983 (Amended 2005).
  2. World Intellectual Property Organization (WIPO). Malaysia’s patent landscape overview.
  3. Malaysian Intellectual Property Corporation (MyIPO). Patent database and guidelines.
  4. Yang, K. (2018). "Pharmaceutical Patents in Southeast Asia," Journal of IP Law.
  5. Global Data on Pharmaceutical Patent Filings. WIPO statistics, 2022.

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