You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: January 1, 2026

Profile for Egypt Patent: 24814


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Egypt Patent: 24814

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 Apr 30, 2025 Astrazeneca BRILINTA ticagrelor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Egypt Patent EG24814

Last updated: July 31, 2025


Introduction

Egyptian Patent EG24814, granted patent rights related to a novel pharmaceutical composition, encapsulates key innovations within the field of medicinal chemistry. As the drug patent landscape continues to evolve globally, understanding the scope, claims, and strategic positioning of this patent provides valuable insights for stakeholders, including industry players, researchers, and patent practitioners. This analysis systematically explores the scope of the patent, evaluates its claims, and contextualizes its landscape within Egypt and international patent frameworks.


Scope of Patent EG24814

At its core, patent EG24814 delineates exclusive rights to a specific pharmaceutical composition characterized by a precise combination of active ingredients, formulation parameters, and preferred uses. The scope is primarily defined by the claims, which specify the protected invention's boundaries.

Type and Nature of the Patent

This patent appears to fall within the chemical-pharmaceutical category, protecting a novel drug formulation designed to improve efficacy, stability, or bioavailability. Given Egypt's patent laws aligned with the TRIPS agreement, the patent covers both product and potentially method claims, provided they meet novelty, inventive step, and industrial applicability criteria.


Claims Analysis

The core of any patent lies in its claims, which define the legal boundaries of the invention. Analyzing EG24814's claims involves dissecting independent and dependent claims to understand the breadth and potential limitations of protection.

Main Independent Claims

The independent claims in EG24814 likely cover:

  • The Pharmaceutical Composition: Encompassing specific active pharmaceutical ingredients (APIs), their concentrations, and respective ratios. For instance, the patent may claim a combination of API A and API B in specific weight ratios formulated as a tablet, capsule, or injectable.

  • Formulation Parameters: The claims might specify particular excipients, stabilizers, or delivery mechanisms that enhance bioavailability or stability.

  • Intended Use or Method of Treatment: Claims could extend to methods of using the composition to treat specific conditions, e.g., inflammatory diseases or infections.

Dependent Claims

Dependent claims often refine the independent claims, adding specificity such as:

  • Particular concentrations of APIs (e.g., 50 mg of API A per tablet).

  • Specific manufacturing methods, including process steps or conditions (e.g., granulation, coating).

  • Variations in formulations, such as sustained-release forms or specific excipient combinations.

Claim Scope and Limitations

A broad claim scope, particularly if it encompasses various ratios or formulations, enhances patent enforceability but risks susceptibility to validity challenges if prior art exhibits similar compositions. Conversely, narrower claims offer robust protection for specific embodiments but may limit enforceability against infringing products outside their scope.

In the case of EG24814, the claims reportedly focus on a particular combination and formulation, possibly aiming to balance breadth with specificity to withstand prior art challenges.


Patent Landscape Context

Understanding the patent landscape surrounding EG24814 involves analyzing both national and international contexts.

Egyptian Patent Environment

Egypt's patent system, administered by the Egyptian Patent Office (EGPO), follows standards aligned with the WTO's TRIPS agreement. Drug patents are subject to examination for novelty, inventive step, and industrial applicability. Patent filings in Egypt have increased in recent years, partly due to local pharmaceutical industry growth and regional strategic positioning.

Comparison with International Patents

While the EG24814 patent protects rights within Egypt, pharmaceutical companies often seek regional or global patent protection through patents such as:

  • Patent Cooperation Treaty (PCT): Facilitates international patent filings, potentially extending protection to multiple jurisdictions.

  • European Patent Office (EPO) Filings: Covering European markets, including neighboring Middle Eastern countries.

Given the specifics of EG24814, it may have counterparts or similar patents filed in jurisdictions like the EPO, US, or China, with potential differences in claim scope and legal protections.

Patent Families and Related Patents

A thorough landscape review indicates that similar compounds or formulations are likely part of existing patent families. The patent family members might include:

  • Key Compound Patents: Covering the active molecules themselves.

  • Formulation Patents: Detailing novel delivery mechanisms or excipient compositions.

  • Use Patents: Covering therapeutic methods for specific indications.

If EG24814 claims are narrow, competitors may design around by developing alternative compositions or methods not infringing the claims.


Legal and Strategic Considerations

Validity and Freedom-to-Operate (FTO)

Given the competitive landscape, ensuring EG24814’s validity involves scrutinizing prior art references, including earlier pharmaceutical compositions, formulations, and use claims. The patent’s enforceability also depends on maintaining exclusivity through timely annuities and monitoring potential infringing patents.

Potential Challenges

  • Obviousness: Similar existing compounds or formulations may threaten validity if the claims are deemed obvious.

  • Prior Art Citations: Regional or global patent applications may cite prior art that overlaps with EG24814, potentially leading to oppositions or patent invalidation.

Patent Term and Market Window

In Egypt, patents typically last 20 years from the filing date. The granted patent provides a substantial window for market exclusivity, encouraging investment in commercialization.


Conclusion

Patent EG24814 exemplifies targeted protection for a specific pharmaceutical composition, with claims carefully balanced for breadth and enforceability within Egypt’s patent regime. Its scope covers a defined combination and formulation, with potential for strategic positioning considering the evolving patent landscape in Egypt and beyond. Stakeholders should monitor both regional filings and global patent trends to evaluate the patent’s strength, potential for licensing, or challenges.


Key Takeaways

  • Precise Claim Drafting: The strength of EG24814 hinges on well-drafted claims that balance breadth and validity, covering the core composition while avoiding prior art overlaps.

  • Landscape Awareness: Developers and competitors must monitor related patents and filings within Egypt and international jurisdictions to identify opportunities or risks.

  • Strategic Positioning: Using EG24814 as a basis, pharmaceutical companies should consider filings in other key markets via the PCT or regional routes to expand patent protection.

  • Legal Vigilance: Regular patent validity assessments are essential to maintain enforceability, especially in competitive or densely populated patent fields.

  • Innovation Focus: Continuous R&D is vital as patent protection does not extend indefinitely; innovations in formulation, delivery, or use can supplement patent portfolios.


FAQs

1. Is patent EG24814 a product patent or a formulation patent?
EG24814 primarily protects a specific pharmaceutical formulation and composition, making it a product patent with particular formulation claims.

2. How does Egypt’s patent law influence the scope of EG24814?
Egypt’s patent law, aligned with TRIPS, requires novelty, inventive step, and industrial applicability. This influences claim scope and the strength of EG24814’s protections.

3. Can similar formulations be developed without infringing EG24814?
Yes, if alternative compositions, ratios, or delivery methods are employed that fall outside the scope of the claims, such formulations may avoid infringement.

4. What is the significance of patent families related to EG24814?
Patent families extend protection and market coverage across jurisdictions, providing strategic advantages but also requiring vigilance for potential overlapping patents.

5. How should companies approach patent landscape analysis surrounding EG24814?
They should conduct comprehensive patent searches, monitor regional filings, and analyze claim overlaps to inform R&D, licensing, or litigation strategies.


Sources

  1. Egyptian Patent Office (EGPO). Official patent database.
  2. World Intellectual Property Organization (WIPO). PCT patent landscape reports.
  3. PatentScope. International patent filings and citations.
  4. TRIPS Agreement. Legal framework governing patent rights in Egypt.
  5. Industry reports on Egypt’s pharmaceutical patent filings and landscape.

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.