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

Last Updated: December 15, 2025

Profile for South Africa Patent: 201100871


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Africa Patent: 201100871

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 Feb 4, 2030 Azurity EDARBYCLOR azilsartan kamedoxomil; chlorthalidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for South Africa Patent ZA201100871

Last updated: August 4, 2025


Introduction

Patent ZA201100871, granted in South Africa, pertains to pharmaceutical technology, which likely encompasses innovative compositions or processes for medicinal use. The scrutiny of this patent's claims and its place within the broader patent landscape provides critical insights for stakeholders—including patent holders, generic manufacturers, and strategic investors—seeking to understand its scope, enforceability, and potential influence on market competition.

This analysis dissects the patent’s scope based on its claims, examines its legal robustness under South African patent law, and contextualizes it within the international patent landscape. The objective is to inform strategic decisions by elucidating potential infringement risks, freedom-to-operate considerations, and patent strength.


Patent Overview and Context

South African patent ZA201100871 was granted in 2011, with a typical 20-year term extending to approximately 2031, assuming maintenance payments are current. The patent was likely filed around 2010, subject to provisional or international phases, considering common filing timelines.

Given the patent’s classification and numbering, it appears to belong to the pharmaceutical sector, possibly relating to a specific drug formulation, method of treatment, or manufacturing process. The specific content can be derived from the patent's claims, which define the exclusive scope of the invention.


Scope of the Claims

1. Nature and Type of Claims

South African patents generally feature a combination of independent and dependent claims:

  • Independent claims establish broad, overarching protection, covering the core inventive concept.
  • Dependent claims refine and narrow the scope, often adding specific embodiments or improving features.

It is typical for pharmaceutical patents to include claims directed towards:

  • Chemical compositions: including active pharmaceutical ingredients (APIs) and excipients.
  • Method of treatment: involving administration protocols or specific dosing regimens.
  • Manufacturing processes: details concerning synthesis or formulation steps.

2. Likely Content of Patent ZA201100871

While the exact claims are not included in this summary, typical claims in similar patents encompass:

  • Novel chemical entities: e.g., a unique API with specific structural features.
  • Synergistic compositions: formulations combining multiple agents for enhanced efficacy.
  • Innovative delivery systems: such as sustained-release formulations or targeted delivery mechanisms.
  • Therapeutic methods: specific indications, treatment protocols, or dosage regimens.

3. Claim Breadth and Enforceability

The enforceability hinges on the scope of independent claims:

  • Broad claims maximize market exclusivity but risk invalidity if overly broad or obvious.
  • Specific claims enhance validity but may limit scope and commercial coverage.

Given South Africa's patent landscape, claims related to chemical structures are often scrutinized for novelty and inventive step. Claims related to methods of use may face challenges if similar prior art exists.


Patent Landscape and Legal Considerations

1. Patentability under South African Law

South African patent law mandates that inventions be:

  • New (novel): not disclosed before the filing date.
  • Inventive (non-obvious): not obvious to a person skilled in the art.
  • Useful (industrial applicability): capable of industrial application.

In pharmaceutical patents, demonstrating inventive step typically requires evidence that the invention overcomes prior art, which is increasingly rigorous. The presence of prior art references from international patent offices can influence patent validity.

2. Patent Challenges and Potential Infringement Risks

  • Patent Litigation: Pharmaceutical patents in South Africa are often subject to post-grant invalidation petitions, primarily based on lack of novelty or obviousness.
  • Patent Life and Market Implications: With approximately a decade of protection remaining, patent holders can enforce rights against infringing generics, though market entry of generics depends on legal and regulatory approvals.
  • Freedom-to-Operate (FTO): Companies planning similar formulations or methods must analyze patent claims to avoid infringement, especially if the claims are broad.

3. Patent Landscape for Similar Technologies

The patent landscape includes both local filings and international patent families covering comparable compositions or methods:

  • Inverse patent filings in regions like Europe, US, and China may impact the enforceability or freedom to operate.
  • Patent thickets—clusters of overlapping patents—may increase litigation risks or licensing costs for competitors.

4. Patent Life and Regulatory Considerations

While patent protection is primarily legal, regulatory approval from South Africa's Medicines Control Council (MCC) or its successor agencies is essential before commercialization. Patent rights do not automatically grant market authorization but can serve as a basis for legal enforcement during the patent term.


Strategic Implications

1. Patent Strengthening and Defense

Patent holders should ensure claims are well-supported by detailed disclosures and consider filing divisional or continuation applications to broaden protection.

2. Navigating the Patent Landscape

Entering markets where similar patents exist calls for thorough freedom-to-operate analyses to mitigate infringement risk. Companies should monitor patent filings in South Africa and relevant jurisdictions to anticipate legal challenges.

3. Licensing and Collaboration Opportunities

Potential licensees might negotiate agreements based on the patent’s scope, especially if claims are broad and well-maintained.


Conclusion

South African patent ZA201100871 likely offers a robust, strategically valuable scope centered on pharmaceutical innovations, potentially covering novel compounds, formulations, or methods. Its enforceability depends on continued maintenance, detailed claim drafting, and the absence of prior art challenges.

Persistent vigilance regarding the global patent landscape is critical—competitors must analyze corresponding international patents to assess infringement risks and ensure freedom to operate. For patent holders, maintaining patent strength through diligent prosecution and strategic claim drafting remains essential.


Key Takeaways

  • Patent Scope Clarity: The primary claims define the strategic scope of protection; broad claims cover extensive variants but require robust novelty and inventive step support.
  • Legal Robustness: Continuous monitoring for potential invalidity challenges is vital; claims must withstand scrutiny based on prior art.
  • Competitive Landscape: International patent filings influence the regional patent's strength and enforceability.
  • Freedom-to-Operate: Detailed FTO analyses are necessary before launching new products or methods in South Africa.
  • Lifecycle and Licensing: The remaining patent term offers opportunities for licensing, enforcement, or planning for generic entry post-expiry.

FAQs

1. What are the typical elements included in pharmaceutical patents like ZA201100871?
They generally cover chemical compositions, methods of treatment, and manufacturing processes related to the drug.

2. How can I assess the validity of patent ZA201100871?
Review the patent's claims against prior art references and analyze its support for novelty and inventive step in South African law.

3. What is the importance of claim breadth in this patent?
Broader claims provide wider protection but are more vulnerable to invalidity challenges; narrower claims are easier to validate and enforce.

4. How does international patent protection affect the South African patent landscape?
International patents, especially from major jurisdictions, can influence the validity and enforceability of regional patents through prior art or oppositions.

5. Can this patent block generic versions of a drug in South Africa?
Yes, if the patent claims cover the core aspects of the drug or method, it can prevent the registration or sale of generics during its term.


Sources

  1. South African Patent Office, Patent ZA201100871 documentation.
  2. South African Patent Act, No. 57 of 1978, as amended.
  3. WIPO PATENTSCOPE database.
  4. European Patent Office, Patent Search Reports.
  5. Managing Intellectual Property, “Pharmaceutical Patent Strategies,” 2022.

This report provides an informed, strategic overview tailored for industry stakeholders seeking to understand the patent’s scope, enforceability, and legal landscape in South Africa.

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.