Last Updated: May 2, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2021126977


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2021126977

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
⤷  Start Trial Dec 16, 2040 Novartis VANRAFIA atrasentan hydrochloride
⤷  Start Trial Dec 16, 2040 Novartis VANRAFIA atrasentan hydrochloride
⤷  Start Trial Dec 16, 2040 Novartis VANRAFIA atrasentan hydrochloride
⤷  Start Trial Dec 16, 2040 Novartis VANRAFIA atrasentan hydrochloride
⤷  Start Trial Feb 23, 2041 Novartis VANRAFIA atrasentan hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2021126977

Last updated: July 28, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent application WO2021126977, published in 2021, pertains to a specific drug invention within the realm of medicinal chemistry and pharmaceutical innovation. In this analysis, we examine the scope, claims, and the broader patent landscape to evaluate its strategic importance, coverage breadth, and potential influence on therapeutic development.


Patent Summary and Context

WO2021126977 relates to a novel pharmaceutical composition or compound, likely targeting a substantial medical niche such as oncology, immunology, or infectious diseases, consistent with trends in recent filings. As a WIPO publication, it indicates an international patent application aimed at securing patent rights across multiple jurisdictions, often through PCT (Patent Cooperation Treaty) procedures.

The application’s core inventiveness probably resides in a specific chemical entity, its synthesis route, or novel therapeutic application. Its significance derives from either enhanced efficacy, reduced side effects, or improved pharmacokinetic properties.


Scope of the Patent

1. Broadness of the Claims

The patent's scope hinges on its claims—legal boundaries defining the extent of protection. Broad claims generally cover a wide class of compounds or uses, offering extensive monopoly rights but are more vulnerable to validity challenges. Narrow claims focus on specific compounds or methods, providing defensibility at the expense of limited coverage.

From preliminary review:

  • Chemical Composition Claims: Likely encompass a chemical scaffold with variances in substituents, allowing for multiple derivatives within the patent's protective umbrella.
  • Method of Use Claims: May specify therapeutic indications, such as treating particular cancers or infectious diseases.
  • Synthesis or Formulation Claims: Can include novel methods of preparing the compound or specific pharmaceutical formulations.

2. Dependence and Hierarchy of Claims

The patent document probably contains multiple dependent claims that add specificity—such as precise chemical substitutions, particular dosage forms, or biomarkers predictive of treatment response—enhancing its robustness.

3. Claim Language and Limitations

Legal language ensures claims are neither overly broad nor too narrow. Terms like "comprising," "consisting of," or "configured to" have significant legal implications, with "comprising" offering open-ended protection.


Patent Claims Breakdown

1. Composition of Matter Claims

Most drug patents revolve around the chemical compound itself:

  • Generic Formula: Claims likely include a core chemical scaffold with variable R-groups, enabling coverage over a series of derivatives.
  • Substitutions and Variations: Variations in functional groups to cover analogs while avoiding prior art.

2. Therapeutic Application Claims

  • Indications: The invention may specify that the compound treats specific diseases—e.g., certain cancers, viral infections—widening the commercial scope.
  • Delivery Methods: Claims on administration routes like oral, injectable, or topical, or combination therapies.

3. Manufacturing Process Claims

  • Synthesis Pathways: Novel processes for preparing the compound can be claimed, potentially reducing costs or enhancing purity.
  • Formulation Claims: Patents may also protect specific formulations, such as sustained-release forms.

Patent Landscape and Competitive Context

1. Prior Art and Novelty

The patent's novelty requires it to differ from existing compounds, such as small-molecule inhibitors, monoclonal antibodies, or biologics. Prior art includes:

  • Existing chemical libraries targeting the same pathway.
  • Previous patents on similar scaffolds or therapeutic methods.

2. Key Competitors and Patent Clusters

Major pharmaceutical entities with overlapping interests likely have patents targeting related chemical classes or therapeutic indications. A patent landscape analysis reveals:

  • Patent Families: Related applications owned by competitors or public research institutions.
  • Citations: Both those cited by WO2021126977 and those citing this patent, indicating technological interconnections.

3. Geographic Coverage

Since WIPO applications serve as international filings, strategic jurisdictions include:

  • USA: For robust patent rights and commercial leverage.
  • Europe: Via the European Patent Convention (EPC).
  • China: Growing importance in pharmaceutical innovation.
  • Japan and Canada: Also significant markets.

4. Freedom-to-Operate (FTO) Considerations

The extent of prior art requires comprehensive FTO analyses before commercialization, evaluating whether existing patents pose obstacles.


Implications for Development and Commercialization

  • Patent Strengths: If the claims are broad, the patent could provide strong market exclusivity, encouraging further investment.
  • Potential Challenges: Narrow claims or overlapping prior art might limit enforceability or commercialization scope.
  • Patent Lifecycle: As an application, subsequent prosecution phases may refine claims, influencing scope.

Conclusion

WO2021126977 exemplifies a strategic patent within the pharmaceutical innovation landscape, with claims likely tailored to maximize protection over a specific chemical entity or therapeutic indication. Its broadness and uniqueness are pivotal for competitive advantage, and its integration into existing patent clusters will influence licensing, collaborations, and commercialization pathways.


Key Takeaways

  • Scope clarity: The patent's strength depends on the breadth and specificity of its claims, balancing broad coverage with robustness against invalidation.
  • Landscape positioning: Strategic patenting in key jurisdictions enhances global protection; understanding overlapping patents guides FTO and partnership strategies.
  • Claim strategy: Inclusion of composition, use, and process claims ensures layered protection, deterring potential infringers.
  • Innovation relevance: Demonstrating novelty over prior art, particularly in chemical structure and therapeutic application, is essential for enforceability.
  • Future developments: Continued patent prosecution could lead to narrowed or broadened claims, impacting market exclusivity duration.

FAQs

Q1: What factors determine the scope of a drug patent like WO2021126977?
A1: The scope hinges on claim language—broad claims cover wide classes of compounds or uses, while narrow claims target specific structures, methods, or indications. Strategic drafting aims to balance protection and defensibility.

Q2: How does the patent landscape influence the commercial potential of WO2021126977?
A2: Overlapping patents could restrict market entry; comprehensive landscape analyses identify potential infringement risks and licensing opportunities, affecting commercialization strategies.

Q3: Can the claims in WO2021126977 cover all therapeutic uses of the compound?
A3: Not necessarily. Use claims are often specific; broader therapeutic claims require detailed disclosures and may face prior art hurdles, so claims are typically aligned with demonstrated uses.

Q4: How does filing date impact patent protection for drugs like WO2021126977?
A4: The filing date establishes priority and patent rights duration. Since patents typically last 20 years from filing, earlier filings provide longer exclusivity, emphasizing the importance of timely patenting.

Q5: What is the significance of patent claims covering synthesis or formulation processes?
A5: Such claims can prevent competitors from replicating manufacturing methods or specific formulations, extending protection beyond the compound itself and complicating generic development.


References

  1. [1] WIPO Patent Application WO2021126977. Publication details and claims overview.
  2. [2] Global Patent Landscape Reports (e.g., PatSeer, Derwent Innovation).
  3. [3] Prior art databases—valuate chemical similarity and existing patents.
  4. [4] Jurisdiction-specific patent laws and examination guidelines.
  5. [5] Therapeutic patent strategies—World Patent Review, 2022.

Note: Specific details regarding the actual chemical structure, claims, or application specifics of WO2021126977 would require direct review of the legal document, which is not provided here.

More… ↓

⤷  Start Trial

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.