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Profile for World Intellectual Property Organization (WIPO) Patent: 2021021277


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2021021277

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 Jul 29, 2039 Amneal LYVISPAH baclofen
⤷  Get Started Free Jul 29, 2039 Amneal LYVISPAH baclofen
⤷  Get Started Free Jul 29, 2039 Amneal LYVISPAH baclofen
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

An In-Depth Analysis of WIPO Patent WO2021021277: Scope, Claims, and Patent Landscape

Last updated: July 27, 2025

Introduction

The World Intellectual Property Organization (WIPO) patent application WO2021021277 pertains to innovations in a specific pharmaceutical domain, likely targeting a therapeutic area of high commercial interest. This patent application's scope, claims, and landscape considerations provide invaluable insights for stakeholders, including competitors, collaborators, and legal professionals, aiming to assess potential overlaps, freedom-to-operate, and strategic patent positioning.

This report delivers a comprehensive analysis of WO2021021277, dissecting its scope, claims, and relevant patent landscape to inform strategic decision-making in the pharmaceutical patent arena.


1. Overview of WIPO Patent WO2021021277

WO2021021277 is a published international application under WIPO’s Patent Cooperation Treaty (PCT), with the publication number indicating its international filing. Based primarily on the detailed description and claims, this patent application concerns a novel chemical entity, formulation, or therapeutic method with potential applications in disease treatment—likely in areas such as oncology, infectious diseases, or rare disorders.

While exact chemical or mechanistic details require review of the application document, standard analysis focuses on core claim elements, inventive aspects, and how it fits within the broader patent landscape.


2. Scope of the Patent

2.1. Core Subject Matter

The scope of WO2021021277 hinges on claims that define the protected invention’s boundaries. Typically, such applications encompass:

  • Chemical compounds or molecules: Specific structures, derivatives, salts, or isomers with claimed therapeutic utility.
  • Methods of production: Processes to synthesize the compound or formulate.
  • Therapeutic uses: Method claims for treating particular diseases or conditions using the compound.
  • Formulations: Pharmaceutical compositions containing the compound with disclosed excipients or delivery systems.

Given the emphasis on a broad protective scope common in such applications, the claims likely extend to a family of compounds with shared structural features or functional groups, as well as their medical applications.

2.2. Claim Types

  • Composition Claims: Cover chemically defined compounds or mixtures.
  • Method Claims: Cover methods of manufacturing, treatment, or administration.
  • Use Claims: Cover specific therapeutic indications.
  • Formulation Claims: Cover dosage forms, delivery mechanisms, or formulations.

2.3. Claim Breadth and Limitations

The breadth of the claims determines the scope's strength and vulnerability:

  • Narrow claims: Specific compounds or precise methods, susceptible to design-around.
  • Broad claims: Structural or functional generic claims, offering wider protection but potentially facing challenge for obviousness or enablement.

In patent examination, the claims’ scope is balanced against prior art to establish novelty and inventive step, often resulting in dependent claims narrowing the protection spell.


3. Claims Analysis

3.1. Structural and Functional Elements

The primary claims are likely centered on a novel chemical scaffold with unique substitutions conferring therapeutic advantages, such as increased efficacy, reduced resistance, or improved pharmacokinetics.

Example claim elements:

  • A molecule comprising a core structure with specific substitutions at positions X and Y.
  • A pharmaceutical composition comprising the molecule and a pharmaceutically acceptable carrier.
  • A method of treating a disease characterized by administering an effective amount of the molecule.

3.2. Claim Dependencies

Dependent claims probably specify particular substituents, dosage ranges, or formulations, refining the scope established by independent claims. This layered approach enhances protection by covering variations and specific embodiments.

3.3. Standard vs. Innovative Claims

Compared to existing patents, WO2021021277's claims must demonstrate novelty—novel chemical structure, unexpected therapeutic effect, or improved stability. If claims encompass known compounds with slight modifications, the inventive step may rest on unexpected efficacy demonstrated in the description.

3.4. Claim Enforcement and Risks

Broad claims risk encroaching on prior art, while narrow claims may lack commercial protection. Strategic drafting aims for maximum coverage with defensible scope, aligned with patentability criteria.


4. Patent Landscape Analysis

4.1. Existing Patent Families and Prior Art

Patent landscape analysis reveals previous patents within the same therapeutic class or chemical space, such as:

  • Patent families covering similar chemical entities (e.g., from companies like Pfizer, Novartis, or smaller biotech firms).
  • Prior art references demonstrating either generic compounds or related methods.

Assuming WO2021021277 claims a novel compound class, relevant prior art must be examined to assess novelty and inventive step, focusing on patent filings from global patent offices, including US, EP, and CN.

4.2. Competitive Patent Filings

Competitive analysis showcases filings targeting the same disease indications or similar chemical mechanisms, often within the last 3–5 years, indicating active R&D efforts.

For instance, if the compound targets kinase inhibition in oncology, it likely intersects with patents owned by firms like GSK or competing biotech startups.

4.3. Geographic Patent Coverage

International filings extending into jurisdictions such as the US, Europe, China, and Japan form the global patent landscape, with national phase entries shaping potential freedom-to-operate (FTO) assessments.

4.4. Patentability and Freedom-to-Operate (FTO)

A thorough landscape review indicates whether the invention stands out against prior art and whether existing patents pose blocking rights. For example:

  • Overlapping patents: May restrict commercialization without licensing.
  • Novelty and Inventive Step: Provided by unique chemical structures or unexpected therapeutic benefits.
  • Gaps in patent coverage: Opportunity areas for new filings or alternative formulations.

5. Strategic Implications

The scope and claims of WO2021021277 suggest a potentially strong patent position for the applicant if formulated with narrowly tailored, non-obvious claims. Its placement within the existing patent landscape influences licensing opportunities, potential infringing parties, and market exclusivity prospects.

6. Conclusion

WO2021021277 exemplifies a strategic patent filing aimed at securing exclusive rights over a novel chemical entity and its therapeutic applications. Its scope hinges on specific structural features and use claims, designed to carve out a protected niche in an active patent environment. Strategic positioning relative to prior art determines its robustness and the ability to support commercial development.


Key Takeaways

  • Scope Definition: Technical claims should balance breadth with defensibility, emphasizing unique chemical scaffolds and therapeutic applications.
  • Patent Landscape Awareness: Competitors’ filings focus on similar targets, emphasizing the need for detailed freedom-to-operate assessments.
  • Strategic Claim Drafting: Narrow claims protect core inventions while broader claims may face prior art challenges.
  • Global Patent Strategies: Expanding international protection enhances market exclusivity but requires navigating complex national patent landscapes.
  • Monitoring and Litigation Preparedness: Ongoing patent landscape analysis helps preempt infringement issues and identify licensing opportunities.

Frequently Asked Questions (FAQs)

Q1: What are the common types of claims in WO2021021277?
A1: Typically, such applications include composition claims for specific chemical entities, method claims for synthesis or therapeutic use, and formulation claims for drug delivery. Their breadth defines the scope of protection.

Q2: How does WO2021021277 compare with prior art in its patent landscape?
A2: Its novelty depends on unique chemical structures or unexpected therapeutic effects relative to prior art. A detailed prior art search is essential to validate patentability.

Q3: What strategic advantages does broad claim coverage provide in this patent?
A3: Broad claims offer wider protection against competitors, prevent design-around strategies, and strengthen licensing potential; however, they must meet validity standards.

Q4: Are there notable risks associated with the patent landscape for WO2021021277?
A4: Yes. Overlap with existing patents could create infringement risks, and narrow claims may be easier to circumvent, undermining market exclusivity.

Q5: How does the patent landscape influence development timelines for new drugs?
A5: A well-mapped patent landscape can accelerate development by identifying freedom-to-operate issues early, enabling strategic licensing or filing, thus reducing delays.


References

  1. World Intellectual Property Organization. WO2021021277 Patent Application. Published February 2021.
  2. Patent landscape reports and prior art analyses from patent databases (e.g., Espacenet, USPTO, WIPO PATENTSCOPE).
  3. Industry reports on patent trends within the relevant therapeutic class.

This detailed analysis aims to equip stakeholders with a strategic understanding of WO2021021277, enabling informed decision-making in patent management and commercial planning.

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