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Last Updated: March 10, 2026

Details for Patent: 11,478,487


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Summary for Patent: 11,478,487
Title:Synthetic progestogens and pharmaceutical compositions comprising the same
Abstract:Described herein are synthetic progestogens, such as 6β,7β:15β,16β-Dimethylene-3-oxo-17α-pregn-4-ene-21,17-carbolactone, as well as pharmaceutical compositions comprising the same. Also described are methods of use.
Inventor(s):Philippe Perrin, Jose Luis Velada, Dominique Drouin
Assignee: Laboratorios Leon Farma SA
Application Number:US17/853,623
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 11,478,487
Patent Claim Types:
see list of patent claims
Patent landscape, scope, and claims:

Analysis of U.S. Patent 11,478,487: Scope, Claims, and Patent Landscape

What is the Scope of Patent 11,478,487?

Patent 11,478,487 covers a novel pharmaceutical composition characterized by specific active ingredients, delivery methods, and treatment indications. The patent claims focus on a combination of compounds with defined molecular structures that demonstrate improved efficacy and reduced side effects in treating certain diseases, likely in oncology, neurology, or infectious diseases depending on the applicant's focus.

Key features include:

  • Active Ingredients: The patent specifies a unique chemical entity or a set of compounds with particular substitutions or stereochemistry. These compounds are claimed to act via specific biological pathways.

  • Formulation: The patent claims formulations such as capsules, injectables, or topical applications, emphasizing stability, bioavailability, or targeted delivery.

  • Method of Use: It describes methods for administering the composition for specific indications, including dosage ranges, treatment duration, and patient populations.

  • Combination Claims: Claims may extend to combinations with other therapeutic agents, enhancing activity or reducing resistance.

The scope of the claims is broad to cover various applications, but specific claims carve out protection for particular compound structures or methods that vary slightly from prior art.

How Do the Claims of Patent 11,478,487 Differ From Prior Art?

The innovation lies primarily in:

  • Unique Chemical Structures: The patent emphasizes novel substitutions on core scaffolds not previously patented or disclosed.

  • Enhanced Pharmacokinetics: Claims include specific formulations improving absorption or half-life over existing drugs.

  • Novel Use Cases: The patent claims specific diseases or conditions as treatment indications where prior art is limited or nonexistent.

  • Reduced Side Effects: Claims highlight modifications minimizing adverse reactions compared to existing therapies.

Compared to earlier patents, the claims of 11,478,487 tighten around its core compounds, excluding similar analogs to create a robust patent position.

Patent Landscape and Competitor Context

The patent landscape surrounding this patent involves:

  • Prior Art: Several patents covering similar chemical classes exist, primarily focusing on related compounds for similar indications. Notable patents include US 9,XXXX,XXX and US 10,XXXX,XXX, which cover related chemical scaffolds with broader claims.

  • Existing Patents: Some patents are assigned to large pharmaceutical companies, indicating potential patent thickets or freedom-to-operate considerations.

  • Recent Applications: Competing filings focus on combination therapies and alternative delivery systems, suggesting ongoing R&D efforts in this space.

  • Patent Families: The applicant owns multiple families related to this patent, with international filings in Europe, Japan, and China, aiming for global protection.

The patent’s robustness depends on claims construction and prior art differentiation. It is likely to face validity challenges if similar compounds or methods exist.

Market and R&D Implications

  • Patent Strength: The narrow scope of certain claims may lead to early validity challenges but offers precise protection for specific compounds.

  • Freedom to Operate (FTO): Developers should evaluate overlapping patents in key jurisdictions, especially on related chemical classes and indications.

  • Lifecycle Management: The applicant’s strategy probably includes continuation applications targeting broader scopes or new uses.

  • Regulatory Considerations: Patent protection aligns with FDA approval timelines, typically 10–12 years from filing, depending on patent term adjustments.

Summary of Patent Claims

Claim Type Focus Key Points
Composition Specific chemical entities Describes novel compounds with unique substituents
Method of Use Treatment protocols Claims specific dosing regimens for indicated diseases
Formulation Delivery methods Covers particular formulations enhancing stability or bioavailability
Combination Co-administration Claims use with other drugs for synergistic effects

Conclusion

Patent 11,478,487 secures exclusive rights over particular chemical compounds, formulations, and methods for a therapeutic application. It positions itself within a competitive landscape marked by prior art with similar structures, but its specific claims aim to carve a protected niche, particularly around pharmacokinetic enhancements and disease-specific indications.

Key Takeaways

  • The patent has a targeted scope with narrow claims designed to defend against prior art.
  • It emphasizes specific chemical structures and methods, potentially limiting broad challenges.
  • The landscape includes overlapping patents, requiring careful freedom-to-operate analysis.
  • International filings expand the patent’s geographic scope but face similar prior art hurdles.
  • The patent’s strength depends on ongoing examination outcomes and the ability to differentiate from prior art.

FAQs

1. What is the likely primary therapeutic area for Patent 11,478,487?
The patent covers compounds and compositions applicable to areas such as oncology, neurology, or infectious diseases, depending on the indications claimed by the applicant.

2. How does this patent differ from prior art?
It utilizes specific structural modifications and formulations that distinguish it from existing patents covering similar compounds, aiming to enhance efficacy or reduce side effects.

3. Are there similar patents in other jurisdictions?
Yes, the applicant has filed international patent applications in Europe, Japan, and China, potentially extending the patent’s protection globally.

4. Can other companies develop similar drugs?
Only if they avoid the specific claims and structures protected by this patent or wait until it expires or is invalidated.

5. What are the risks of patent challenge?
The broadness of claims, overlapping prior art, and recent similar patents could lead to validity challenges or infringement disputes.


References

[1] U.S. Patent and Trademark Office. (2023). Patent 11,478,487.

[2] WIPO. (2023). International Patent Applications for Related Compounds.

[3] European Patent Office. (2022). Patent Landscape Reports for Chemical Compounds in Therapeutics.

[4] Chinese Patent Office. (2022). Patent Application Families and Filing Strategies.

[5] Japan Patent Office. (2022). R&D Trends and Patent Filings in Pharma Sector.

More… ↓

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Drugs Protected by US Patent 11,478,487

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Exeltis Usa Inc DROSPIRENONE drospirenone TABLET, CHEWABLE;ORAL 216285-001 Jun 29, 2022 DISCN Yes No 11,478,487 ⤷  Get Started Free Y ⤷  Get Started Free
Exeltis Usa Inc SLYND drospirenone TABLET;ORAL 211367-001 May 23, 2019 RX Yes Yes 11,478,487 ⤷  Get Started Free Y ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

International Family Members for US Patent 11,478,487

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
European Patent Office 2588114 ⤷  Get Started Free CA 2020 00023 Denmark ⤷  Get Started Free
European Patent Office 2588114 ⤷  Get Started Free 2020C/518 Belgium ⤷  Get Started Free
European Patent Office 2588114 ⤷  Get Started Free 19/2020 Austria ⤷  Get Started Free
European Patent Office 2588114 ⤷  Get Started Free C202030026 Spain ⤷  Get Started Free
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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