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

Last Updated: December 31, 2025

Profile for Argentina Patent: 116035


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Argentina Patent: 116035

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
11,633,396 Oct 7, 2029 Astrazeneca LYNPARZA olaparib
11,975,001 Oct 7, 2029 Astrazeneca LYNPARZA olaparib
12,048,695 Oct 7, 2029 Astrazeneca LYNPARZA olaparib
12,144,810 Oct 7, 2029 Astrazeneca LYNPARZA olaparib
12,178,816 Oct 7, 2029 Astrazeneca LYNPARZA olaparib
8,475,842 Dec 31, 2029 Astrazeneca LYNPARZA olaparib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

In-Depth Analysis of Argentine Patent AR116035: Scope, Claims, and Landscape

Last updated: August 3, 2025


Introduction

Patent AR116035, filed within Argentina's intellectual property framework, pertains to a specific pharmaceutical innovation. As the Latin American country adheres to the TRIPS Agreement via its national legislation, patent rights generally encompass novel, inventive, and industrially applicable drug-related inventions. Analyzing AR116035’s scope and claims provides insights into its strategic positioning within the patent landscape, potential market exclusivity, and implications for competitors and innovators.


Patent Scope of AR116035

The scope of patent AR116035 revolves around its detailed claims, which define the boundaries of exclusivity. Typically, pharmaceutical patents fall into categories such as compound patents, formulation patents, methods of use, and manufacturing processes.

While the full text of AR116035 is proprietary and not explicitly available publicly, based on standard patent law practices and available patent databases, several aspects can be inferred:

  • Main Focus: The patent likely claims a novel chemical entity, a new formulation, or an innovative method of treatment. Its scope extends to how the drug is made, used, or administered, and the specific chemical structures or process steps involved.]

  • Claims Breadth: Given the common structure of pharmaceutical patents, AR116035 probably includes independent claims covering the core compound or method, with dependent claims specifying particular variations, dosages, or excipient combinations.

  • Claim Type and Strength: The broader the independent claims, the wider the protection. If the claims are narrowly tied to a specific chemical derivative or method, competitors may develop around it. Conversely, broader claims offer extensive coverage but may face higher invalidity risks.


Analysis of the Claims

An effective patent analysis includes examining the scope and robustness of the claims, which often fall into these categories:

1. Composition of Matter Claims

If AR116035 claims a new chemical compound, these are foundational and typically provide the strongest patent protection. Such claims aim to prevent competitors from manufacturing and marketing the same compound.

  • Claim language likely encompasses the compound's structure, including specific substituents, stereochemistry, or molecular weight ranges.
  • Implications: Stronger protection against generics, provided the compound demonstrates novelty and inventive step.

2. Method-of-Use Claims

Method claims often specify the particular medical application of the compound, such as treating a specific disease or condition.

  • Scope: These claims protect not only the compound but also specific indications, enhancing exclusivity.
  • Limitations: They are often narrower and susceptible to design-around strategies.

3. Formulation and Manufacturing Claims

Claims covering formulation innovations (e.g., controlled-release matrices) or manufacturing processes aim to secure additional layers of protection.

  • Benefit: They can extend patent life beyond compound patents if the formulation offers significant therapeutic or stability advantages.

4. Combination Claims

If the patent covers combinations with other compounds or excipients, it broadens potential applications and market segments.


Patent Landscape in Argentina

Argentina exhibits a dynamic pharmaceutical patent environment influenced by national innovation policies and international treaties, notably the TRIPS Agreement. Its patent law, aligned with TRIPS, emphasizes:

  • Novelty and Non-Obviousness: Strict criteria for patentability.
  • Patent Term: 20 years from filing, subject to maintenance fees.
  • Granting Process: Examination is substantively rigorous, focusing heavily on novelty and inventive step.

Current Landscape Highlights

  • Major Players: Multinational pharmaceutical companies actively patent new drugs in Argentina, often seeking patent protection for innovative compounds, formulations, and methods.
  • Patent Trends: The country has witnessed an increase in patent filings covering biologics, combination therapies, and specific formulations, reflecting industry focus.
  • Patent Challenges: Argentina’s legal framework allows third parties to file opposition and oppositions during patent granting, leading to a rigorous examination process.
  • Compulsory Licenses: Argentina's legislation permits compulsory licensing under public health emergencies, which can impact patent exclusivity.

AR116035 in Context

Given the strategic importance of patent AR116035, its positioning within this landscape hinges on:

  • Patent Family: It is crucial to examine whether AR116035 is part of a broader family covering related compounds or formulations, enhancing defensive and offensive IP strategies.
  • Legal Status and Maintenance: Ensuring maintenance fees are paid sustains its enforceability.
  • Litigation and Licensing: Potential enforcement actions or licensing agreements can influence its commercial trajectory.

Strategic Implications

The scope of AR116035's claims determines its defensibility and market potential:

  • Narrow Claims: Easier to defend but offer limited market exclusivity.
  • Broad Claims: Provide extensive coverage but may face invalidation or challenges based on prior art.
  • Patent Lifecycle Management: Combining compound, formulation, and method claims optimizes protection duration.

Competitors aiming to develop similar drugs must analyze whether their innovations infringe upon the claim scope, while innovators should explore licensing or research-around strategies.


Conclusion

Patent AR116035 appears to represent a strategically valuable pharmaceutical patent within Argentina’s evolving patent landscape. Its scope, primarily defined by its claims—whether composition, method, or formulation—dictates its enforceability and competitive impact. A thorough examination of its claims, legal status, and related patent family members is vital for stakeholders to navigate the Argentine pharmaceutical patent terrain effectively.


Key Takeaways

  • Scope Precision: The strength and breadth of AR116035's claims directly influence its market exclusivity and defensibility.
  • Patent Family Strategy: Broadening claims across patents enhances protection and bargaining power.
  • Landscape Awareness: Firms should monitor Argentina’s legal climate, including potential for compulsory licenses and opposition proceedings.
  • Portfolio Management: Combining compound, formulation, and method claims extends lifecycle and reduces vulnerability.
  • Legal Vigilance: Regular patent maintenance and enforcement are crucial amid Argentina’s active patent environment.

FAQs

1. What are the typical components of a pharmaceutical patent claim in Argentina?
Claims generally cover chemical compounds (composition of matter), methods of use, formulation specifics, and manufacturing processes, all subject to Argentine patent law standards for novelty and inventive step.

2. How does Argentina’s patent law influence pharmaceutical patents like AR116035?
Argentina requires substantive examination, emphasizing novelty and non-obviousness, with provisions for compulsory licensing and opposition, shaping the scope and enforcement of patents.

3. Can competitors develop similar drugs despite AR116035’s patent?
Yes, if they innovate around the claims—such as creating structurally different compounds, alternative formulations, or different methods—without infringing the patent.

4. How does the patent landscape in Argentina impact patent strategy for pharmaceutical companies?
It necessitates comprehensive patent portfolio planning, including broad claims, family expansion, and ongoing legal vigilance to sustain market exclusivity.

5. What is the significance of patent AR116035 in Argentina’s pharmaceutical market?
Its significance depends on the patented compound's therapeutic value, scope of claims, and the company's ability to enforce and maintain the patent, affecting competitive positioning.


Sources:

[1] Argentine Patent Office (INPI). Official Patent Documents.
[2] WIPO. Argentina Patent Law and Practice.
[3] World Trade Organization. TRIPS Agreement Overview.
[4] Patent databases (e.g., Espacenet, INPI national registry).

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.