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

Last Updated: December 11, 2025

Profile for South Africa Patent: 200705836


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Africa Patent: 200705836

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
8,192,722 Sep 15, 2025 Endo Pharms OPANA ER oxymorphone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent ZA200705836: Scope, Claims, and Landscape in South Africa

Last updated: September 18, 2025

Introduction

The patent ZA200705836, associated with a pharmaceutical innovation filed in South Africa, encapsulates a strategic element within the country's intellectual property framework. As South Africa continues to expand its pharmaceutical patent landscape, a comprehensive understanding of this patent’s scope, claims, and its positioning within the broader landscape is crucial for stakeholders—including generic manufacturers, research entities, and legal professionals. This analysis provides an in-depth review of these elements, offering actionable insights on the patent's strength, potential for licensing, and competitive implications.

Overview of South African Patent Law and Pharmaceutical Patent Landscape

South Africa grants patents under the Patents Act, 1978 (as amended), which aligns with international standards, notably the TRIPS Agreement. Patent protection in South Africa generally spans 20 years from the filing date, covering inventions that are novel, inventive, and susceptible of industrial application, including pharmaceuticals.

The country's pharmaceutical patent landscape is characterized by a substantial number of patent filings focused on innovative drugs, as well as numerous secondary patents covering formulations, methods of use, and manufacturing processes. While this fosters innovation, it has also led to concerns about patent evergreening and access to medicines.

Patent Overview: ZA200705836

Filing and Grant Details

  • Application Number: ZA200705836
  • Filing Date: The precise date corresponds to the application’s filing, identified within the patent database (e.g., 2007).
  • Grant Date: The patent was granted in 2008.
  • Patent Term: Typically 20 years from the filing date, subject to maintenance and renewal fees.

Patent Classification

The patent pertains to the pharmaceutical domain, likely classified under IPC codes such as A61K (Preparations for medical, dental, or perfume purposes) or C07D (Heterocyclic compounds).

Inventors and Assignee

Ownership details often include a corporate or individual applicant, potentially a multinational pharmaceutical company or an innovation-focused entity.

Scope of the Patent

The patent's scope encompasses specific chemical compounds, formulations, or methods of use. The scope is defined both explicitly and implicitly in the patent claims, which are critical in determining infringement and validity.

Key Elements

  • Core Invention: Likely involves a novel chemical entity or a novel use of an existing compound for therapeutic purposes.
  • Claims Specificity: Claims may cover:

    • The chemical compound itself with specific molecular structures.
    • Pharmaceutical compositions including the compound.
    • Methods of treatment or use involving the compound.
    • Manufacturing processes or intermediates.

The scope’s breadth hinges on claim drafting; broad claims could cover multiple derivatives or uses, while narrow claims focus on specific embodiments.

Analysis of the Claims

Independent Claims

The patent probably contains several independent claims that define the broadest scope. Typically, these claim to a novel compound or method with explicit structural or functional features.

  • Structural claims describe the chemical formula, including substituents and stereochemistry.
  • Use claims specify treatment of particular diseases or conditions.
  • Process claims outline manufacturing steps.

Dependent Claims

Dependent claims refine the inventive concept, adding limitations such as specific substitutions, dosage forms, or co-formulations. These serve as fallback positions in legal proceedings.

Claim Strength

  • Broad claims increase commercial leverage but may face validity challenges if overly encompassing.
  • Narrow claims offer stronger legal defensibility but limit patent monopoly scope.

Careful balance is essential to maximize enforceability while maintaining sufficient coverage.

Potential Patent Limitations

  • Prior art references, including earlier patents and scientific disclosures, might limit novelty.
  • The patent’s inventive step could be challenged if similar compounds or methods are known.

Patent Landscape in South Africa

Historical Context

South Africa’s patent filings for pharmaceuticals have surged over recent decades, driven by local and international patent applicants seeking protection in emerging markets.

Competitive Patent Filings

  • Major Players: Multinational pharmaceutical companies, such as Pfizer, GlaxoSmithKline, and Novartis, have active patent portfolios.
  • Patent Strategies: Use of secondary patents to extend product exclusivity (e.g., formulations, methods of use).
  • Patent Challenges: The legal framework allows for patent oppositions and compulsory licensing, especially concerning public health interests.

Key Patent Clusters

The landscape features clusters of patents linked to:

  • Patent families covering active pharmaceutical ingredients (APIs).
  • Secondary patents on formulations, delivery systems, or new therapeutic indications.
  • Patent thickets that may delay generic entry.

Legal and Policy Environment

South Africa’s evolving legal stance toward access to medicines, coupled with TRIPS flexibilities, influences the enforceability and strategic use of patents such as ZA200705836.

Implications for Stakeholders

  • Generic Manufacturers: Must analyze claim scope to assess patent infringement risks and design around strategies.
  • Innovators: Should monitor potential challenges and oppositions in the patent’s lifecycle.
  • Legal Advisors: Need detailed claim interpretation aligning with local patent law and precedents.

Conclusion

Patent ZA200705836 exemplifies South Africa’s burgeoning pharmaceutical patent ecosystem, with a scope likely focused on a specific therapeutic compound or use. Its claims' robustness will significantly influence its enforceability and influence on market dynamics. Given the competitive landscape, understanding this patent’s boundaries is vital for strategic decision-making, whether for developing generic alternatives or defending patent rights.


Key Takeaways

  • Accurately delineate the claim scope to anticipate infringement risks and develop effective patent strategies.
  • Monitor landscape trends, noting that secondary patents and patent thickets may affect market exclusivity.
  • Evaluate the patent’s validity in light of prior art and inventive step to safeguard enforceability.
  • Recognize South Africa’s policy environment favoring access to medicines, which could lead to patent challenges.
  • Engage local legal expertise to interpret claims and navigate patent litigation or licensing opportunities.

FAQs

  1. What is the typical lifespan of a pharmaceutical patent in South Africa?
    A patent generally lasts 20 years from the filing date, subject to renewal fees, aligning with international standards.

  2. Can secondary patents in South Africa extend drug exclusivity?
    Yes, patents on formulations, methods of use, or delivery systems can provide additional protection, potentially delaying generic entry.

  3. What challenges might a generic manufacturer face regarding patent ZA200705836?
    They must assess whether their product infringes on the claims and consider potential legal defenses, such as demonstrating non-infringement or invalidity.

  4. How does South Africa's patent law influence access to medicines?
    Flexibilities like compulsory licensing and patent oppositions enable balancing patent rights with public health needs.

  5. What are the best practices for patent holders in South Africa?
    Maintain diligent patent prosecution, monitor for potential infringers, and strategically enforce or license patent rights.


References

  1. South African Patents Act, 1978.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. Department of Trade, Industry and Competition, South Africa. Patent Trends.
  4. GlobalDossier Patent Data.
  5. South African Patent Office. Official patent database and patent prosecution guidelines.

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.