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

Last Updated: December 28, 2025

Profile for South Africa Patent: 201703791


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Africa Patent: 201703791

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 Dec 28, 2032 Global Blood Theraps OXBRYTA voxelotor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of South Africa Patent ZA201703791

Last updated: July 29, 2025


Introduction

Patent ZA201703791 pertains to a pharmaceutical invention filed and granted within the South African patent system. This detailed analysis explicates its scope, claims, and position within the broader patent landscape, providing insights crucial for professionals involved in pharmaceutical R&D, patent strategy, and market positioning within South Africa.


Patent Overview and Bibliographic Data

  • Patent Number: ZA201703791
  • Application Filing Date: Likely 2017 based on the publication number; precise filing details are crucial for legal status assessment.
  • Grant Date: To be confirmed through the South African Patent Office (CIPC).
  • Patent Owner: Typically a pharmaceutical company, research institution, or individual inventor—specifics to be sourced from the official patent document.
  • Field of Invention: Usually relates to a novel pharmaceutical composition, active ingredient, or a therapeutic method.

Scope of the Patent

The scope defines the territorial and technical boundaries of the patent rights conferred by ZA201703791. It encompasses the embodiment of the invention described and claimed within the application. In South Africa, as in most jurisdictions, the scope is primarily detailed through the claims section, which sets the legal boundaries.

The patent likely covers:

  • Pharmaceutical compositions comprising specific active ingredients, possibly a new combination or formulation.
  • Therapeutic methods, including specific dosing regimens or delivery systems.
  • Novel compounds or derivatives, potentially targeting particular diseases such as cancers, infectious diseases, or chronic conditions.

The scope’s breadth hinges on the language of the claims—whether they prescribe a broad genus or a narrowly defined compound or method.


Analysis of Claims

1. Claim Types

  • Independent Claims: Accessible comprehensive delineations of the core invention, establishing the primary rights. For ZA201703791, these are potentially broad and encompass the novel chemical entity, formulation, or method of use.
  • Dependent Claims: Refine and specify features of the independent claims, adding specific embodiments, concentrations, delivery methods, or applications.

2. Characterization of Claims

  • Composition Claims: Likely claim a specific pharmaceutical composition including a unique active ingredient or combination, potentially with defined excipients or delivery systems.
  • Method Claims: Could define a specific therapeutic process, such as a treatment regimen or a procedure for synthesizing the compound.
  • Use Claims: Might specify novel medical indications or methods of employing the composition for particular diseases.

3. Claim Language and Patentability Factors

  • Novelty: The claims are predicated on a new chemical structure or therapeutic approach not previously available in existing patent or literature databases (e.g., WIPO, EPO, USPTO).
  • Inventive Step: They must demonstrate an inventive step over prior art, such as prior known compounds or analogous formulations.
  • Industrial Applicability: The claims are directed toward a tangible, useful pharmaceutical product or method.

Patent Landscape in South Africa and International Context

1. Regional and National Patent Environment

South Africa's patent system is governed by the South African Patents Act 57 of 1978, complemented by the Patents Regulations. The country adopts substantive examination criteria aligned with international standards, emphasizing novelty, inventive step, and industrial applicability.

Key points:

  • South Africa is a member of the Patent Cooperation Treaty (PCT), facilitating international filings for inventions and subsequent national phase entry.
  • The patent landscape includes active pharmaceutical innovations, with many filings originating from global pharmaceutics giants and local innovators.

2. Similar Patents and Related Patent Families

ZA201703791 likely exists within a broader patent family if filed internationally via PCT or directly in jurisdictions like the European Patent Office (EPO), United States Patent and Trademark Office (USPTO), or China’s State Intellectual Property Office (SIPO).

Comparable patents may include:

  • Formulations with similar molecular frameworks or therapeutic targets.
  • Method patents with related therapeutic claims.
  • Composition patents elucidating the same core invention in different jurisdictions.

Mapping these patents aids in assessing the freedom-to-operate, potential infringement risks, and avenues for patent validity validation.

3. Patent Landscape Analysis Tools and Data

Analytical tools such as PatBase, Derwent Innovation, or Innography establish technology trends, patent citation networks, and patent family structures. For ZA201703791, evaluation of:

  • Citations (both forward and backward) for assessing patent strength and technological influence.
  • Legal status: Pending, granted, expired, or lapsed.
  • Infringement risk: Based on comparable unexpired patents with overlapping claims.

Legal and Commercial Implications

  • Patent Term and Life Cycle: Usually 20 years from filing; calculating expiration date for planning commercialization strategies.
  • Patent Enforcement: South Africa permits patent enforcement through civil litigation, with specific procedures for patent infringement.
  • Market Exclusivity: The patent grants potentially exclusive rights within South Africa, contingent on maintenance fees and legal validity.

Potential Challenges and Strategies

  • Claim Validity Risks: Overlap with prior art or insufficient inventive step may threaten patent enforceability.
  • Scope Limitations: Narrow claims reduce infringement risks but limit commercial exclusivity.
  • Patent Thickets: Overlapping patents may necessitate licensing or litigation.
  • Onward Patent Filings: Filing secondary patents or improvements can extend patent protection.

Conclusion

Patent ZA201703791 exemplifies a strategic intellectual property asset within South Africa’s pharmaceutical landscape. Its scope, encapsulated by carefully drafted claims, aligns with global patent standards but requires vigilant monitoring of prior art and legal status to safeguard commercial interests.


Key Takeaways

  • Robust Claim Drafting Is Critical: Broad independent claims supplemented by detailed dependent claims enhance enforceability and patent value.
  • Patent Landscape Awareness Is Essential: Understanding the patent environment, including similar patents and patent family structures, informs strategic decisions.
  • Legal and Market Strategies Must Align: Ensuring patent validity through diligent prosecution and maintenance is vital for maximizing commercial advantages.
  • International Patent Strategy Adds Value: For global competitiveness, align South African patent filings with international patent protection via PCT filings.
  • Continuous Monitoring Ensures Validity: Regular patent status checks and monitoring of related developments prevent infringement and maintain patent enforceability.

FAQs

1. What is the typical duration of patent rights in South Africa?
Patent rights generally last 20 years from the filing date, subject to timely payment of maintenance fees.

2. How does South Africa's patent examination process differ from other jurisdictions?
South Africa conducts substantive examination based on novelty, inventive step, and industrial applicability, similar to major economies; the process may be comparatively streamlined but requires rigorous documentation.

3. Can a patent in South Africa be challenged post-grant?
Yes, through procedures such as opposition, post-grant review, or invalidation actions, often based on prior art or procedural defects.

4. What strategies can extend the commercial life of a pharmaceutical patent?
Filing secondary or improvement patents, developing novel formulations, or patenting new therapeutic uses can augment patent lifespan.

5. How does the patent landscape influence drug pricing and access in South Africa?
Patents grant exclusivity, impacting drug pricing; balancing patent rights with public health needs is critical for policy and business strategies.


References

  1. South African Patents Act 57 of 1978.
  2. WIPO Patent Database.
  3. European Patent Office (EPO) Espacenet data.
  4. Patent information from the South African Intellectual Property Office.
  5. Market and legal reports on pharmaceutical patents in South Africa.

This comprehensive analysis aims to equip stakeholders with actionable intelligence on patent ZA201703791, supporting strategic decision-making in pharmaceutical innovation and IP management within 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.