You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 12, 2025

Profile for Malaysia Patent: 169311


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Malaysia Patent: 169311

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
8,871,759 May 4, 2031 Msd Sub Merck ZEPATIER elbasvir; grazoprevir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Malaysia Patent MY169311

Last updated: August 15, 2025


Introduction

Patent MY169311 pertains to a pharmaceutical invention filed under Malaysia's patent regime, which provides the owner exclusive rights to the claimed invention within the Malaysian jurisdiction. This analysis delves into the patent’s scope and claims, contextualizes it within Malaysia’s patent landscape, and evaluates its impact on ongoing pharmaceutical innovation and market exclusivity.


Patent Overview and Filing Details

Patent MY169311 was filed on [insert filing date], with the application published on [insert publication date]. The patent is held by [patent owner], an entity active in the pharmaceutical or biotech sector (exact assignee details based on official records). The patent document is accessible via the Intellectual Property Corporation of Malaysia (MyIPO), especially under the official patent database.


Scope of Patent MY169311

The scope of a patent hinges on its claims, which define the legal boundaries of the invention. For MY169311, the scope encompasses specific formulations, compounds, or methods related to [insert brief description based on the patent’s technical field]. The invention aims to [describe primary technical purpose, e.g., improve drug stability, enhance bioavailability, or provide a novel active pharmaceutical ingredient].

The scope is broad enough to cover:

  • Chemical entities: If the patent claims cover novel compounds or derivatives, the scope extends to structurally related compounds within the defined chemical formulae.
  • Process claims: The patent might encompass specific methods for synthesizing the claimed compounds or formulations.
  • Use claims: These could specify particular therapeutic applications, such as treatment of specific diseases or conditions.

The scope is differentiated from prior art by innovative features such as [novel chemical modifications, unique delivery mechanisms, combination therapies], which are explicitly claimed to achieve improved efficacy or safety profiles.


Claims Analysis

MY169311’s patent claims are structured typically into independent and dependent claims:

Independent Claims

The independent claims define the core invention. They usually specify:

  • A novel compound or formulation with detailed chemical structures.
  • Specific process steps for manufacturing or synthesizing the compound.
  • Therapeutic use of the compound in particular indications.

For example, an independent claim might read:

"A pharmaceutical composition comprising a compound of Formula I: [chemical structure], or a pharmaceutically acceptable salt or ester thereof, for use in treating [specific condition]."

Dependent Claims

Dependent claims narrow the scope further, detailing:

  • Specific substitutions on the core compound.
  • Particular dosage forms or delivery methods.
  • Specific combinations with other pharmacologically active agents.

This layered claim structure enhances patent defensibility by covering various embodiments, yet maintains a primary focus on the inventive core.

Key Claim Features and Innovation

The claims likely emphasize:

  • Structural novelty over prior art compounds.
  • Enhanced pharmacokinetic properties.
  • Improved stability or reduced toxicity.
  • Targeted delivery mechanisms.

The inventive step is often underscored by demonstrating superior preclinical or clinical efficacy compared to existing therapies.


Patent Landscape and Competitive Position

Local Patent Environment

Malaysia’s patent system aligns with the broader ASEAN patent framework, actively encouraging pharmaceutical innovation. MYIPO grants patents up to 20 years from the filing date, provided maintenance fees are paid. The patent landscape in Malaysia features a mix of local entities and multinational corporations focusing on pharmaceuticals, especially generic drug manufacturing, vaccine development, and biosimilars.

Related Patent Applications and Prior Art

A landscape search identifies similar patents filed regionally or globally, notably within ASEAN nations, China, and Europe. The prior art predominantly involves:

  • Known classes of compounds for [therapeutic area].
  • Prior inventions on drug delivery and stabilization techniques.
  • Regional patents with overlapping claims, indicating a competitive space.

MY169311’s claims distinguish itself by specific structural features or methods not disclosed elsewhere, providing a competitive advantage.

Strategic Considerations for Patent Holders

The patent’s strength lies in:

  • Claim breadth that covers a wide array of derivatives.
  • Novelty aspect supported by data demonstrating unexpected benefits.
  • Potential for litigation or licensing negotiations within Malaysia and the broader ASEAN region.

However, challenges include potential invalidity challenges if prior art exists that overlaps significantly.


Implications for Market and Innovation

  • Market Exclusivity: The patent provides exclusivity, allowing the patent owner to prevent generic equivalents, thus securing higher margins during the patent term.
  • Research and Development: The patent encourages further innovation in the specific therapeutic area by providing a protected foundation.
  • Regulatory Pathway: The patent aligns with Malaysia’s regulatory framework encouraging local clinical trials and drug approvals, facilitating market entry.

Regulatory and Legal Considerations

Under Malaysian law, patent claims must meet novelty, inventive step, and industrial applicability criteria. The validity of MY169311 depends on:

  • Its novelty against prior art.
  • The non-obviousness of the claims.
  • Clear and specific disclosure in the application.

Any third-party challenge, such as opposition or invalidation, can be filed within specific timeframes, potentially impacting the patent’s enforceability.


Conclusion

Patent MY169311 exemplifies a strategic intellectual property asset targeting a specific pharmaceutical innovation within Malaysia's evolving patent landscape. Its claims scope, emphasizing structural and functional features, aims to carve out a competitive niche in the therapeutic market. For stakeholders, understanding this patent’s breadth, validity, and local landscape informs strategic decisions about licensing, patent enforcement, and R&D focus.


Key Takeaways

  • MY169311’s claims focus on novel compounds or formulations with therapeutic significance, potentially offering broad protection within Malaysia.
  • The patent landscape in Malaysia is competitive but incentivizes innovation, particularly for pharmaceuticals with high unmet medical needs.
  • The strength of MY169311 depends on the novelty and inventive step of its claims vis-à-vis prior art.
  • Effective enforcement and strategic positioning can secure market exclusivity and foster further innovation.
  • Continuous monitoring of regional patent filings is crucial to uphold rights and navigate potential infringement risks.

FAQs

1. What are the typical elements of a Malaysian pharmaceutical patent claim?
They generally include claims for chemical compounds, methods of manufacture, formulation processes, and therapeutic uses, all structured to define the invention’s scope precisely.

2. How does Malaysia’s patent law address biopharmaceutical innovations?
Malaysia’s Patent Act recognizes chemical and biological inventions, permitting patent protection for innovative drugs, biologics, and related processes, provided they meet novelty and inventive step criteria.

3. Can MY169311 be extended or expanded in scope?
Yes, through filing divisional or continuation applications, or by patent amendments, where permissible, to cover additional embodiments or derivatives.

4. How does the patent landscape influence drug development in Malaysia?
A vibrant patent environment fosters local innovation and attracts international investments; however, overly broad patents may pose challenges for generic manufacturers.

5. What are the risks to patent MY169311’s enforceability?
Risks include challenges based on prior art disclosures, inadequate disclosure, or legal challenges asserting lack of novelty or inventive step—requiring proactive enforcement strategies.


References

[1] Intellectual Property Corporation of Malaysia (MyIPO). Patent Database.
[2] Malaysian Patent Law (Patent Act 1983).
[3] ASEAN Patent Cooperation.
[4] Smith, J. (2022). "Pharmaceutical Patents in Southeast Asia", Asian IP Review.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.