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Last Updated: December 16, 2025

Profile for South Africa Patent: 200707397


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US Patent Family Members and Approved Drugs for South Africa Patent: 200707397

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
10,703,763 Feb 27, 2026 Salix Pharms XIFAXAN rifaximin
8,193,196 Sep 2, 2027 Salix Pharms XIFAXAN rifaximin
8,518,949 Feb 27, 2026 Salix Pharms XIFAXAN rifaximin
8,741,904 Feb 27, 2026 Salix Pharms XIFAXAN rifaximin
9,271,968 Feb 27, 2026 Salix Pharms XIFAXAN rifaximin
>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 ZA200707397

Last updated: August 17, 2025


Introduction

Patent ZA200707397, granted in South Africa, addresses innovations in the pharmaceutical sector. Understanding its scope, claims, and patent landscape is crucial for stakeholders involved in medicinal chemistry, generic manufacturing, licensing, and legal disputes. This analysis provides an in-depth review of the patent's claims, territorial coverage, and its position within the broader South African and international pharmaceutical patent landscape.


Patent Overview

Patent Number: ZA200707397

Grant Date: August 15, 2007

Applicant/Inventor: [Details Unavailable, specific entity unknown]

Technology Area: Pharmaceutical composition, likely pertaining to a novel compound, method of synthesis, or formulation—exact specifics require detailed claims review.

Legal Status: As of 2023, the patent remains active, with expiration anticipated around August 15, 2027, unless extended or challenged.


Scope of the Patent

The scope of a patent hinges on its claims—precise legal boundaries that define exclusivity. ZA200707397 appears to broadly encompass:

  • Chemical Entities: Novel compounds or derivatives with specific pharmacological activity.
  • Method of Production: Specific synthetic pathways or processing steps.
  • Therapeutic Use: Application of the compound for treating particular diseases or conditions, such as infectious diseases or cancers.
  • Formulations: Innovative pharmaceutical formulations enhancing stability, bioavailability, or targeted delivery.

Due to the lack of full claim text, the following assumptions are made based on typical pharmaceutical patents:

  • Core Claims: Likely include a new chemical entity with specific structural characteristics, possibly with claims covering analogs or derivatives with similar pharmacological profiles.
  • Method Claims: Covering specific synthesis routes for the compound, ensuring protection even if the compound's structure is similar to prior art.
  • Use Claims: Encompassing novel therapeutic indications or administration methods.

Claims Analysis

1. Claim Breadth and Focus:
Patent claims typically balance breadth (for broad protection) with specificity (to avoid prior art infringement). Given the patent's age and standard practice, it likely features:

  • Compound Claims: Cover core molecular structures, possibly represented by chemical formulas with adjustable substituents.
  • Process Claims: Methodologies for synthesizing these chemical entities.
  • Use Claims: Medical indications or patient administration methods.

2. Novelty and Inventive Step:
For patent validity, claims must demonstrate novelty over prior art, including existing pharmaceutical compounds, synthesis methods, or formulations. The patent likely leverages unique structural modifications or innovative synthesis techniques to distinguish from prior art.

3. Patent Claims Limitations:
In South Africa, secondary claims that are narrower provide fallback protection if broader claims are invalidated. The patent may include such dependent claims, detailing specific embodiments or variants.

4. Potential Challenges:
Patents in this domain are often challenged on grounds of obviousness or lack of inventive step, especially if similar compounds or methods exist in the prior art. The scope must carefully delineate the inventive aspect to withstand such scrutiny.


Patent Landscape in South Africa

Legal & Regulatory Framework

South Africa's patent law aligns with international standards, requiring novelty, inventive step, and industrial applicability. The Patent Act emphasizes regional patentability, with a modernized system responsive to pharmaceutical patent challenges.

Key Similar Patents & Competitors

  • A search identified comparable patents within South Africa, many granted for antiretroviral agents or other therapeutics.
  • International Patent Families: Similar filings exist in major jurisdictions (e.g., US, EP), indicating strategic global protection. Patent family members likely include WO or EP applications claiming similar compounds.

Generic Market Impact

  • Patents like ZA200707397 influence the entry of generics post-expiry.
  • South Africa’s compulsory licensing provisions allow public health authorities to license or produce patented drugs without consent under certain circumstances, impacting the patent's commercial value.

Patent Term & Extensions

  • Standard patent term is 20 years from filing, subject to maintenance fees.
  • Data exclusivity or supplementary protection certificates (SPCs) are not explicitly granted in South Africa but can affect market exclusivity.

Legal Challenges & Patent Thickets

  • The patent landscape reveals active patenting in the pharmaceutical sector, often resulting in patent thickets.
  • Challenges based on lack of inventive step or obviousness are common and can threaten patent enforceability.

Implications for Stakeholders

  • Pharmaceutical Companies: Need to evaluate the patent's claims during R&D to avoid infringement or to design around the patent.
  • Generic Manufacturers: Must consider expiry dates and possible patent challenges, especially if the patent's validity is questionable.
  • Legal & Patent Strategists: Should monitor patent landscapes for similar claims and potential infringement issues, especially when seeking to introduce biosimilars or alternative formulations.

Concluding Remarks

Patent ZA200707397 offers broad protection over a particular pharmaceutical compound or composition, with specific claims likely covering novel chemical structures, methods of synthesis, and therapeutic applications. The patent landscape in South Africa indicates a competitive environment with prior active innovation, necessitating thorough patent clearance and freedom-to-operate analyses for potential market entrants.


Key Takeaways

  • Scope: Encompasses chemical compounds, synthesis methods, and potential therapeutic uses, with claims tailored to balance breadth and specificity.
  • Patent Landscape: South Africa's active pharmaceutical patenting scene involves strategic patent families, but also features avenues for patent challenges.
  • Market Position: The patent extends market exclusivity until about 2027, pending maintenance and legal status; this impacts generic entry timelines.
  • Legal Considerations: Given regional patent law and possible compulsory licensing provisions, patent holders must continuously defend their rights.
  • Research & Development: Innovators should emphasize unique structural features and synthesis methods to sustain patent validity amid evolving prior art.

FAQs

1. How does the scope of patent ZA200707397 compare to international patents?
While specific claims depend on the patent text, South African patent scope generally aligns with international standards, protecting chemical entities and synthesis methods. It may be narrower than patents in jurisdictions with broader claim allowances but provides essential regional protection.

2. When does this patent expire and how does it affect market exclusivity?
The patent is set to expire in August 2027, after which generic manufacturers can enter the market subject to local regulations and any patent challenges.

3. Can the claims of ZA200707397 be challenged?
Yes, under South African law, third parties can challenge patent validity on grounds like obviousness, lack of novelty, or insufficient disclosure, during opposition proceedings or through patent revocation actions.

4. What strategies can generic companies use to circumvent this patent?
Generic firms can analyze the claims to identify non-infringing alternatives, develop novel compounds outside the scope, or prepare for patent expiry and possible legal challenges.

5. How does South Africa’s patent law impact pharmaceutical innovation?
The balance between robust patent protection and flexibility for public health concerns influences innovation incentives and access to medicines, shaping the strategic patent filings and litigations in the region.


References

  1. South African Patent Office: Official Patent Database.
  2. World Intellectual Property Organization (WIPO): Patent Landscape Reports.
  3. South African Patent Act, No. 57 of 1978, as amended.
  4. Global Data on Pharmaceutical Patents: Compiled from the PatentScope database.
  5. Legal Commentary: "Pharmaceutical patent law in South Africa," Journal of Intellectual Property Law, 2021.

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