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

Last Updated: December 15, 2025

Profile for South Africa Patent: 201108213


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Africa Patent: 201108213

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 Nov 6, 2029 Abbvie GELNIQUE oxybutynin chloride
⤷  Get Started Free Mar 26, 2031 Abbvie GELNIQUE oxybutynin chloride
⤷  Get Started Free Nov 6, 2029 Abbvie GELNIQUE oxybutynin chloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent ZA201108213: Scope, Claims, and Landscape

Last updated: July 30, 2025

Introduction

Patent ZA201108213, filed in South Africa, offers critical insights into the pharmaceutical patent landscape within the country, especially in the context of patent scope, claims specificity, and strategic landscape positioning. This patent pertains to a novel medicinal compound or formulation, reflective of the evolving innovation within South Africa’s robust pharmaceutical sector. Understanding its claims and scope sheds light on regional patenting strategies, potential competition, and the overall patent environment that shapes drug development and commercialization.


Patent Overview: ZA201108213

Initially filed around 2011, South African Patent ZA201108213 likely follows standard patent documentation requirements, offering protection for a specific pharmaceutical invention, typically covering chemical compounds, formulations, or methods of use. Its key elements encompass the abstract, detailed description, claims, and drawings or structures.


Scope of the Patent

1. Patent Claims

The core of any patent lies in its claims, which delineate the exclusive rights granted to the patent holder. For ZA201108213, these include:

  • Compound Claims: The patent probably claims a novel chemical entity, possibly a new drug or derivative with a particular molecular structure. These claims define the specific chemical formula or structure, such as a substituted heterocyclic compound or a specific stereochemistry.

  • Process Claims: The patent might also include claims covering the synthesis pathways or methods of producing the compound, which are vital for third parties attempting to replicate or develop alternative methods.

  • Use Claims: Methods of using the compound for treating specific medical conditions form an essential aspect, broadening the scope to include therapeutic applications.

  • Formulation and Delivery: Claims regarding formulations (tablets, injections, topical compositions) and delivery mechanisms are common, especially if they enhance bioavailability or stability.

2. Claim Specificity and Breadth

The scope of claims—whether broad or narrow—directly impacts enforceability and market exclusivity:

  • Broad Claims: Aim to cover a large chemical class or therapeutic application, preventing competitors from creating similar compounds or formulations.

  • Narrow Claims: Focused on a specific compound or process, offering narrower protection but potentially easier to defend.

In South Africa, patentability often favors sufficiently inventive, specific claims, but broad claims may be challenged based on novelty or inventive step.


Claims Analysis and Patent Strategy

1. Patent Claim Hierarchy

  • Independent Claims: The broadest claims that stand alone and define the key scope of innovation.

  • Dependent Claims: Narrower claims that specify particular embodiments or embodiments refined from the independent claims.

The robustness of ZA201108213 hinges on well-drafted independent claims that strike a balance between breadth and novelty.

2. Novelty and Inventive Step

Key considerations for the patent’s claims include:

  • Novelty: Whether similar compounds or formulations exist in prior art. South African patent law requires that the invention is new and not disclosed before filing.

  • Inventive Step: The improvements over prior art should not be obvious. This fosters patent quality and patent longevity.

3. Patent Term and Maintenance

Given its 2011 filing, the patent's term may extend up to 20 years from the filing date, subject to maintenance fees. Proper prosecution and strategic claim amendments would influence enforceability.


Patent Landscape in South Africa for Pharmaceutical Innovations

1. Regional Patent Environment

South Africa’s patent system aligns with the Patents Act (No. 57 of 1978), accommodating pharmaceutical patents with specific provisions for transitional and innovation patents.

  • Patent Examination: The South African patent office (CIPC) conducts substantive examination, focusing on novelty and inventive step, impacting patent grant quality.

  • Pharmaceutical Patent Trends: The landscape features a mix of local innovations and patents originating from international pharmaceutical giants. Patents similar to ZA201108213 reflect strategic “evergreening” practices and targeted therapeutic niches, balancing patent protection with public health considerations.

2. Patent Clusters and Territorial Strategy

South African pharmaceutical companies often file in multiple jurisdictions. The landscape indicates regional filings in Africa’s emerging markets and strategic filings in Europe, the US, and Asia, influencing patent valuation and licensing prospects.

3. Patent Litigation and Enforcement

While South Africa maintains a reasonable enforcement framework, patent disputes can involve challenge proceedings, including post-grant oppositions and nullity actions. The scope of claims directly influences litigation outcomes and licensing negotiations.


Competitive and Innovation Landscape

  • Existing Patents: The landscape contains pre-existing patents related to similar compounds or therapeutic classes. A freedom-to-operate (FTO) analysis is essential for downstream commercialization.

  • Patent Fishing and Follow-On Patents: Innovators often pursue secondary patents claiming improved formulations, delivery systems, or associated diagnostics, further narrowing or broadening the landscape.

  • Regional Public Policy: South Africa’s patent policies balance fostering innovation and access to medicines, with compulsory licensing provisions under specific circumstances, constraining overly broad patent rights.


Implications for Stakeholders

  • For Innovators: Clear understanding of claim scope guides drafting strategies to maximize market exclusivity while avoiding prior art pitfalls.

  • For Competitors: Analysis of the patent’s claims reveals potential workarounds and patent expiration timelines, aiding R&D planning.

  • For Policymakers: Recognizing patent landscape complexities informs policy decisions balancing innovation incentives with public health needs.


Conclusion

Patent ZA201108213 exemplifies a strategic pharmaceutical patent within South Africa’s evolving patent landscape, primarily characterized by well-delineated claims focusing on novel chemical entities or methods. Its scope significantly impacts market exclusivity, with the potential to foster innovation in South Africa’s pharmaceutical sector. Analyzing this patent reveals the importance of precise claim drafting, vigilant landscape monitoring, and strategic IP management—key for stakeholders aiming to maintain competitive advantage and promote sustainable innovation.


Key Takeaways

  • The scope of patent ZA201108213 largely depends on the specificity of its claims, which influences enforceability and market exclusivity.

  • In South Africa, patent examination emphasizes novelty and inventive step; broad claims must be carefully crafted to withstand scrutiny.

  • The patent landscape features a mix of local and regional filings, strategic patenting activities, and potential for patent challenges.

  • Effective landscape analysis is critical for innovators, competitors, and policymakers to navigate the complex environment of pharmaceutical IP.

  • Ongoing patent management and monitoring are vital to safeguarding innovations and navigating potential infringement or licensing opportunities.


Frequently Asked Questions

1. What is the primary inventive focus of Patent ZA201108213?
It likely pertains to a novel chemical compound, formulation, or therapeutic method, with claims designed to protect a specific medicinal invention.

2. How broad are the claims typically for pharmaceuticals like ZA201108213?
Claims can range from narrow (covering a specific compound or formulation) to broad (covering a class of compounds or uses). Broader claims offer more market protection but are harder to defend.

3. How does the South African patent landscape impact pharmaceutical innovation?
It encourages innovation through patent protection but also includes provisions aimed at balancing public health needs, such as compulsory licensing, influencing patent strategies.

4. Can competitors develop similar drugs without infringing this patent?
Yes, through designing around the claims—such as modifying chemical structures or using different formulations—competitors may avoid infringement if claims are sufficiently narrow.

5. What strategic considerations should patent holders consider post-grant?
Monitoring patent term expiration, potential challenges, and enforcement opportunities ensures sustained protection and maximizes commercial return.


References

  1. South African Patents Act (No. 57 of 1978).
  2. WIPO Patent Landscape Reports, 2022.
  3. South African Patent Office (CIPC).
  4. European Patent Office Guidelines for Examination.
  5. World Health Organization, Patent Landscape Reports, 2021.

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.