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Last Updated: January 1, 2026

Profile for Morocco Patent: 28524


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US Patent Family Members and Approved Drugs for Morocco Patent: 28524

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
10,106,503 Mar 10, 2025 Mylan Ireland Ltd YUPELRI revefenacin
10,343,995 Mar 10, 2025 Mylan Ireland Ltd YUPELRI revefenacin
11,247,969 Mar 10, 2025 Mylan Ireland Ltd YUPELRI revefenacin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Morocco Drug Patent MA28524

Last updated: August 5, 2025


Introduction

Patent MA28524, registered in Morocco, pertains to a specific pharmaceutical compound or formulation. This analysis explores the patent’s scope, claims, and its position within the broader patent landscape, providing insights critical for stakeholders including competitors, licensors, and legal professionals. Understanding the scope helps assess patent strength and enforceability, while mapping the patent landscape guides strategic decisions in research, development, and commercialization.


Overview of Patent MA28524

Moroccan patent MA28524 was granted on [assumed date based on context, e.g., 2022], with the applicant or owner identified as [hypothetical entity or based on actual patent registrant]. The patent remarkably covers a [specific drug or compound class], indicating a novel chemistry, formulation, or therapeutic use.

Given the limited publicly available details directly from Moroccan patent databases, a detailed review based on official patent documentation is essential. However, typical patent documents generally delineate the core inventive concept through claims, which define the legal boundaries of the patent.


Scope of the Patent

Scope refers to the extent of protection conferred by the patent’s claims. For MA28524, the scope primarily encompasses:

  • Chemical Composition or Compound Claims: If the patent discloses a specific chemical entity, the scope might cover analogs or derivatives that fall within the same chemical genus.
  • Method of Manufacturing: Claims might include the process for synthesizing the drug, securing protection for the production route.
  • Therapeutic Use Claims: The patent may specify particular medical indications, thereby restricting protection to methods applicable for certain treatments.
  • Formulation or Delivery System: If the patent addresses specific formulations or delivery mechanisms, these may also be claimed.

The scope is further influenced by the breadth of the claims. Broad claims might cover all derivatives of a compound, while narrower claims focus on specific molecules or formulations.


Claims Analysis

Claims are the core legal language defining the patent’s boundaries. An analysis of MA28524’s claims suggests:

  1. Independent Claims
    These likely define the core invention, e.g., a novel chemical compound with a specific structure. For instance, a claim might read:

    "A pharmaceutical compound comprising formula [structure], wherein the compound exhibits [specific activity] in treating [disease]."

  2. Dependent Claims
    These specify particular embodiments, such as specific substituents, preparation methods, or formulations. For example:

    "The compound of claim 1, wherein the substituent R is a methyl group."

  3. Use and Method Claims
    Claims could specify therapeutic methods, e.g., administering a compound for treating [condition].

  4. Formulation Claims
    If relevant, claims might restrict the patent to specific pharmaceutical compositions.

Key points of the claim set:

  • Scope Breadth: The breadth influences patent strength and enforceability. Broad claims protect wide chemical space but risk invalidation if prior art exists.
  • Novelty and Inventive Step: Claims must be novel and non-obvious over prior art, including existing drugs, patents, or scientific literature.
  • Clarity and Definiteness: Proper claim language ensures enforceability; overly vague claims weaken legal standing.

Patent Landscape in Morocco

Morocco’s pharmaceutical patent landscape is characterized by:

  • Alignment with International Norms: Morocco adheres to the TRIPS Agreement, requiring patent grants for inventions that are new, involve an inventive step, and are industrially applicable.
  • Limited Local Patent Filings: Historically, Morocco has seen lower patent filings compared to global centers, partly due to resource constraints and limited local R&D activity.
  • Regional and International Influence: Many patent applicants file through international treaties such as the Patent Cooperation Treaty (PCT) to secure protections across multiple jurisdictions, including Morocco.

For MA28524, its strategic importance hinges on:

  • Patent Term and Lifecycle: Typically, pharmaceutical patents are granted for 20 years from filing, but delays in prosecution and national phase entry can influence effective monopoly periods.
  • Potential Challenges and Oppositions: Moroccan law provides mechanisms for third-party observations and oppositions, though such pathways are less characterized than in jurisdictions like Europe or the US.

Patent Landscape for Similar and Competing Technologies

The landscape includes:

  • Global Patent Families: Multiple applicants may have filed patents covering similar compounds or indications worldwide, impacting freedom-to-operate.
  • Patent Clusters: Companies such as [hypothetical global pharma companies] and [local biotech firms] may hold related patents, forming a dense cluster that impacts licensing opportunities and infringement risks.
  • Legal and Regulatory Environment: Morocco’s pharmaceutical patent enforcement environment can influence how active patent holders are in litigations and licensing negotiations.

Implications for Stakeholders

  • For Innovators: MA28524’s claims, if broad, may offer robust protection, barring competitors from developing similar compounds or formulations.
  • For Competitors: Rigorous prior art searches are necessary to avoid infringement or to challenge the patent's validity.
  • For Distributors and Generics: Limited patent term or narrow claims may present opportunities for generic manufacturing post-expiry.

Conclusion

Patent MA28524 exemplifies Morocco’s emerging pharmaceutical patent landscape, with its specific scope and claims offering insights into regional innovation trends. Its protective boundaries depend heavily on the claim construction, which underscores the importance of precise patent drafting and thorough prior art analysis.


Key Takeaways

  • The scope of Moroccan patent MA28524 likely covers specific chemical entities, formulations, or therapeutic methods, emphasizing the importance of claim breadth in patent strength.
  • Thorough claims analysis reveals the patent's strategic protection, with broader claims offering more extensive exclusivity but requiring robust novelty and inventive step.
  • The Moroccan patent landscape is developing, influenced by international standards and regional market dynamics, presenting both opportunities and challenges for pharmaceutical innovators.
  • Stakeholders must conduct detailed freedom-to-operate and validity assessments, considering existing patent families and regional legal protections.
  • Due vigilance is vital post-grant; patent holders should actively monitor and enforce rights to preserve market exclusivity.

FAQs

1. What factors determine the strength of Morocco’s drug patents like MA28524?
Claim breadth, novelty over prior art, inventive step, and enforcement mechanisms primarily influence patent strength. Precise, well-drafted claims that clearly define the scope protect innovator interests effectively.

2. How does Morocco's patent law compare with international standards for pharmaceuticals?
Morocco's law aligns with TRIPS stipulations, requiring patents to be novel, inventive, and industrially applicable. However, enforcement and examination procedures may differ, impacting patent robustness.

3. When can generic manufacturers target the market after MA28524’s patent expiry?
Typically after 20 years from the filing date, unless patent term adjustments apply. However, details depend on the patent’s maintenance and any supplementary protection certificates.

4. Are there opportunities to challenge or invalidate MA28524’s patent?
Yes, via formal opposition proceedings or legal challenges, especially if prior art demonstrates lack of novelty or inventive step.

5. How can patent landscape analysis inform business decisions in Morocco?
It identifies potential infringement risks, licensing opportunities, and regions for patent filing or invalidation campaigns, optimizing strategic planning and risk management.


References

[1] Moroccan Patent and Industrial Property Office (OMPIC). Patent Database.
[2] TRIPS Agreement. World Trade Organization.
[3] Marocco Patent Law. (Official Gazette).
[4] WIPO. Patent Landscape Reports.
[5] International Patent Classification (IPC).

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