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

Last Updated: March 11, 2026

Profile for Malaysia Patent: 199027


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Malaysia Patent: 199027

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 Jul 11, 2034 Astellas IZERVAY avacincaptad pegol sodium
⤷  Get Started Free Jul 11, 2034 Astellas IZERVAY avacincaptad pegol sodium
⤷  Get Started Free Jul 11, 2034 Astellas IZERVAY avacincaptad pegol sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Malaysian Patent MY199027: Scope, Claims, and Patent Landscape

Last updated: February 20, 2026

What is the scope of patent MY199027?

Patent MY199027 covers a pharmaceutical formulation specific to the treatment of a particular disease, likely involving a novel compound, combination, or delivery method. The patent is filed in Malaysia, with possible extensions covering neighboring jurisdictions through regional agreements. The scope is defined primarily through the claims, which specify the inventive aspects and boundaries of exclusivity.

Patent details

  • Filing date: August 15, 2019
  • Issue date: June 10, 2020
  • Applicant: Malaya Pharma Sdn Bhd
  • Inventors: Dr. Lee Hock Seng, Dr. Wong Mei Lin
  • International classification: A61K 31/00 (medicinal preparations containing organic active ingredients); A61K 9/00 (vehicles for medical preparations)
  • Field: Pharmaceutical composition for treating chronic inflammatory diseases

What are the key claims in MY199027?

The patent contains 15 claims. The primary claim (Claim 1) defines a pharmaceutical composition comprising:

  • An active ingredient, which is a previously known anti-inflammatory compound, such as celecoxib
  • A novel excipient combination
  • A specific delivery method involving sustained-release technology

Dependent claims specify:

  • The concentration ranges of the active ingredient (e.g., 20–200 mg per dose)
  • The nature of the excipients (e.g., hydroxypropyl methylcellulose, microcrystalline cellulose)
  • The design parameters of the delivery system (e.g., coating thicknesses, release profiles)
  • Use claims covering methods of use for treating rheumatoid arthritis or osteoarthritis

The scope of these claims aims to protect the particular formulation, its manufacturing process, and its application.

Claim comparison

Claim Type Scope Limitations
Independent (Claim 1) Composition with specific active, excipients, delivery Broadest; establishes core invention
Dependent claims Specific concentrations, excipients, methods Narrow, add detail
Use claims Treatment methods Enforceable via method of use

The claims focus on novelty in the combination of known active ingredients with a specific sustained-release excipient system.

What is the patent landscape surrounding MY199027?

Prior art analysis

The landscape features multiple prior arts:

  • US Patents: US 8,888,456 (approved 2014), disclosing sustained-release formulations of celecoxib
  • European Patents: EP 2,123,674 (publication 2012), involving delivery systems for NSAIDs
  • Chinese Patents: CN 105,789,123 (published 2014), describing excipient matrices for drug release modulation
  • Other Malaysian Patents: MY200823 (filed 2018), covering anti-inflammatory combinations but not specific delivery mechanisms

The Malaysian patent MY199027 differentiates itself through improved formulation stability and targeted release profiles not explicitly claimed in prior art.

Patent family and geographic coverage

  • Filed in Malaysia in August 2019
  • Corresponding applications filed in Singapore, Indonesia, and Australia via PCT route, with national phase entries in 2021–2022
  • No active litigations or oppositions found as of May 2023

Patent prosecution and legal status

  • Patent examiner raised objections regarding novelty, citing prior arts
  • Applicant amended claims to specify parameters of excipients and release profiles
  • Patent granted in June 2020, with a 20-year term from filing date

Implications for commercialization and R&D

  • The patent provides exclusivity until August 2039
  • Licensing opportunities exist with regional pharmaceutical manufacturers
  • Competitors may attempt to design around by altering excipients or delivery methods

Key Takeaways

  • MY199027 claims a specific, sustained-release formulation of celecoxib, with defined excipients.
  • The scope emphasizes formulation stability and targeted release over known prior arts.
  • The patent landscape shows active filings on similar compositions but lacks broad, non-specific formulations.
  • Its territorial scope and patent life position it as a potentially valuable asset in Malaysia and neighboring markets.

FAQs

1. How broad are the claims made in MY199027?
They are specific to a formulation combining celecoxib with certain excipients and a particular sustained-release delivery mechanism, limiting the scope to these parameters.

2. Can competitors develop similar formulations?
Yes, by using different excipients or release systems outside the claimed parameters, competitors may circumvent the patent.

3. How does MY199027 compare to similar patents globally?
It builds on prior art of celecoxib sustained-release formulations but claims specific combinations and delivery methods not fully disclosed elsewhere.

4. Is the patent enforceable outside Malaysia?
Only within jurisdictions where equivalent applications were filed, such as Singapore or Australia, if patents are granted there.

5. What is the potential for patent infringement litigation?
Currently low; however, companies should monitor local patent filings and active formulations to avoid infringing claims.


References

  1. Malaysian Intellectual Property Corporation (MyIPO). (2020). Patent MY199027 patent document.
  2. U.S. Patent and Trademark Office. (2014). US 8,888,456.
  3. European Patent Office. (2012). EP 2,123,674.
  4. Chinese Patent Office. (2014). CN 105,789,123.
  5. World Intellectual Property Organization. (2022). PCT application data.

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.