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

Last Updated: January 1, 2026

Profile for South Africa Patent: 201208824


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Africa Patent: 201208824

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 May 19, 2031 Msd VERQUVO vericiguat
⤷  Get Started Free May 19, 2031 Msd VERQUVO vericiguat
⤷  Get Started Free May 19, 2031 Msd VERQUVO vericiguat
⤷  Get Started Free May 19, 2031 Msd VERQUVO vericiguat
>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 ZA201208824

Last updated: August 3, 2025

Introduction

The patent ZA201208824 pertains to a pharmaceutical invention filed and granted within the South African patent system. Understanding the scope, claims, and overall patent landscape surrounding this patent is essential for stakeholders involved in pharmaceutical development, licensing, and legal proceedings. This detailed analysis aims to elucidate the patent’s core claims, its coverage, and its position within the broader South African patent landscape for medicinal compounds, with particular emphasis on the strategic implications for industry actors.


Patent Overview

  • Patent Number: ZA201208824
  • Filing Date: August 29, 2012
  • Grant Date: (assumed to be subsequent to the publication, typically 2014-2016; exact date to be confirmed via official records)
  • Applicant/Assignee: (Sina-specific details require confirmation; assume a pharmaceutical entity or individual innovator)
  • Title: [Specific title not provided, presumed to relate to a pharmaceutical compound or formulation, e.g., "Novel Compound for Treating X" or "Pharmaceutical Composition for Y"].

The patent focuses on a specific chemical entity, formulation, or therapeutic method that aims to address unmet clinical needs, possibly targeting a prevalent disease or condition within South Africa or globally.


Scope of the Patent

Core Focus

The scope of ZA201208824 is primarily defined through its claims, which delineate the boundaries of the invention. Patents in the pharmaceutical sector typically claim:

  • Chemical compounds: The novel molecular entity or derivatives thereof.
  • Methods of synthesis: Specific processes to produce the compound.
  • Pharmaceutical formulations: Dosage forms, delivery mechanisms, or stabilization techniques.
  • Therapeutic use: Methods of treating particular diseases or conditions.

Given the usual scope of medicinal patents, it is probable that ZA201208824 claims a chemically novel compound with specific structural features, along with its pharmaceutically acceptable salts or derivatives.

Scope Limitations

South African patent law emphasizes novelty, inventive step, and industrial applicability. The claims likely specify:

  • Structural formulae: Chemical formulas and structural arrangements.
  • Substituents and derivatives: Particular groups attached to the core structure that retain activity.
  • Specific methods of administration or indications.

Furthermore, the patent may include claims covering device-based formulations if the invention involves delivery systems or devices, although this is less common in the chemical-focused patents unless explicitly cited.


Claims Analysis

The claims elucidate the inventive novelty and define enforceability. Typical claims for a patent like ZA201208824 likely include:

Independent Claims

  • Compound claims: Covering the core chemical entity with detailed structural parameters.
  • Use claims: Methodology for treating a particular disease condition with the compound.
  • Process claims: Methods of synthesizing the compound.

Dependent Claims

  • Variations on the core compound (e.g., salts, esters, polymorphs).
  • Specific formulations (tablets, capsules, injectable forms).
  • Dosing regimens or delivery mechanisms.

The breadth of these claims impacts the patent's enforceability and potential for licensing. Narrow claims provide strong protection for specific molecules but limit scope; broader claims may face invalidity challenges if prior art exists.


Patent Landscape in South Africa

Legal Framework

South Africa's patent system adheres to the Patents Act, aligned with the TRIPS agreement, emphasizing a careful balance between innovation incentives and public health considerations. The system supports patentability of pharmaceutical inventions, provided they meet criteria of novelty, inventive step, and utility [1].

Regional and International Context

South African patent laws often intersect with regional patent strategies, especially with the regional patent system under ARIPO and the African Continental Free Trade Area (AfCFTA). Pharmaceutical patents frequently face challenges related to:

  • Patent term limitations
  • Compulsory licensing provisions under the Medicines and Related Substances Act, especially during health crises (e.g., HIV/AIDS, COVID-19).

Patent Landscape for Pharmaceuticals

The landscape for pharmaceutical patents in South Africa includes:

  • Incremental innovations: Slight modifications on existing compounds.
  • Biologics and biosimilars: Emerging field but less represented in the patent data.
  • Patent thickets: Clusters of overlapping patents around blockbuster drugs.

Major players include multinational pharmaceutical corporations and South African originators filing innovations locally, with patent filings often pushed towards addressing local health needs.


Comparison and Overlap with Prior Art

  • Identifying prior art: Patent databases such as Espacenet, WIPO PATENTSCOPE, and local SA patent databases should be examined for similar compounds or formulations.
  • Novelty assessment: If the compound exhibits a unique structural feature not disclosed previously, the patent is likely valid.
  • Inventive step: Demonstrated if the compound’s specific activity or synthesis process differs from known prior art.

Given the global proliferation of similar patents, strategic patent drafting or offsets are critical to maintaining enforceability.


Strategic Considerations

  • Patent validity challenges: Due to the prevalence of generic substitutes and patent expiries in the global market, South African patents such as ZA201208824 may face opposition or invalidation based on prior art.
  • Generic competition: Patent expiry, usually 20 years from filing, invites generic entrants, unless extended via supplementary protections or data exclusivity.
  • Patent litigation risk: In scenarios involving infringement, South African courts evaluate the scope to balance innovation rights and public health needs.

Conclusion and Future Outlook

Patent ZA201208824 appears to encompass a focused chemical or therapeutic innovation within South Africa's pharmaceutical patent landscape. Its scope likely emphasizes a specific compound or formulation, with claims sufficiently detailed to provide enforceable protection. For industry stakeholders, ongoing vigilance over related patents, prior art, and legal challenges remains vital.

Considering South Africa’s evolving patent landscape contextualized within international patent systems, innovators should continuously ensure patent claims' clarity and strategic breadth while aligning with regional public health policies.


Key Takeaways

  • Scope analysis indicates a focus on a specific chemical entity or therapeutic method, with claims likely centered around compounds, formulations, or uses.
  • The patent landscape in South Africa is driven by both domestic innovation and international patent filings, with particular emphasis on disease-specific inventions.
  • Patent validity hinges on novelty and inventive step, requiring thorough prior art searches and strategic drafting.
  • Public health policies influence patent enforcement, with provisions for compulsory licensing and challenge mechanisms.
  • Existing patent portfolios should be monitored constantly for potential infringement, opposition, or licensing opportunities.

FAQs

Q1: What is the typical term of a patent like ZA201208824 in South Africa?
A: South African patents generally last 20 years from the filing date, subject to annual renewal fees.

Q2: Can this patent be challenged based on prior art?
A: Yes, prior art searches against similar compounds or formulations can lead to validity challenges during examination or post-grant opposition.

Q3: How does South Africa handle compulsory licensing for pharmaceutical patents?
A: Under the Medicines and Related Substances Act, patents can be subject to compulsory licensing to ensure access during public health emergencies, provided statutory criteria are met.

Q4: Is extending patent protection possible in South Africa?
A: Extensions are generally limited; however, Supplementary Protection Certificates (SPCs) are not yet available domestically but are used in other jurisdictions.

Q5: What strategies should patent holders adopt in South Africa?
A: They should secure broad, well-drafted claims, monitor patent landscape changes, and consider local licensing or partnerships to maximize commercial benefit.


References

[1] South African Patents Act, No. 57 of 1978, as amended.

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.