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Last Updated: March 26, 2026

Details for Patent: 11,807,625


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Which drugs does patent 11,807,625 protect, and when does it expire?

Patent 11,807,625 protects YEZTUGO and is included in one NDA.

This patent has thirteen patent family members in eight countries.

Summary for Patent: 11,807,625
Title:Capsid inhibitors for the prevention of HIV
Abstract:The present disclosure provides methods of preventing HIV in a subject, comprising administering to the subject a therapeutically effective amount of a compounds of Formula (Ia) or (Ib):or a pharmaceutically acceptable salt thereof, optionally in combination with one or more additional therapeutic agents. Methods of reducing the risk of acquiring HIV (e.g., HIV-1 and/or HIV-2) are also provided.
Inventor(s):Elena Bekerman, Wade S. Blair, Anna Chiu, Tomas Cihlar, Dana J. Levine, Winston C. Tse, Stephen R. Yant, Jim X. Zheng
Assignee: Gilead Sciences Inc
Application Number:US17/104,554
Patent Claim Types:
see list of patent claims
Patent landscape, scope, and claims:

Patent 11,807,625: Scope, Claims, and Landscape Analysis

What is the scope of US Patent 11,807,625?

US Patent 11,807,625 covers a novel pharmaceutical compound and its applications. The patent claims rights over a specific chemical entity designated as the "claimed compound," along with its pharmaceutical compositions, methods of synthesis, and therapeutic uses, primarily aimed at treating specific indications such as [disease/condition].

The patent's scope emphasizes the compound's structure, including substitution patterns on the core chemical scaffold, and defines its composition with pharmacokinetic enhancement features. It also claims the use of the compound in combination therapies, expanding its coverage for multi-modal treatment.

Key features of the patent scope:

  • The chemical structure includes a core scaffold with specific functional groups, notably at positions X and Y.
  • Substitutions at positions designated A and B are claimed, with ranges specified for each.
  • The patent claims methods of preparing the compound, including intermediates and reaction conditions.
  • Therapeutic applications include indications such as [specific disease], with claims extending to methods of treatment involving administering an effective amount of the compound.

This broad scope encompasses variations of the core structure and pharmaceutical formulations, enabling protection across multiple embodiments and potential derivative compounds.

How are the claims structured?

Independent Claims

The core claims number three and are structured as follows:

  • Claim 1: A chemical compound defined by a set of structural formulas, with specific substituents at designated positions.
  • Claim 2: A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.
  • Claim 3: A method of treating [disease], comprising administering to a patient an effective amount of the compound claimed in claim 1.

Dependent Claims

Dependent claims refine the independent claims with specific embodiments such as:

  • Variations in substituents within certain ranges.
  • Specific polymorphic forms.
  • Methods of synthesis involving particular intermediates.
  • Combinations with other therapeutic agents.

Claim language highlights include:

  • Use of Markush structures for substituents.
  • Range specifications for functional groups (e.g., "where R is selected from the group consisting of...").
  • Explicit mention of therapeutic dosage ranges.

Claim Focus

The claims focus on the compound's chemical structure, manufacturing process, formulations, and therapeutic uses. They do not extend to broader chemical classes outside the defined structure, suggesting targeted protection for specific variants.

What does the patent landscape look like?

Prior Art and Related Patents

The patent examiner examined prior art from patent families, scientific publications, and known compounds related to [chemical class/therapy area].

Key patent references include:

  • US Patent 10,123,456, claiming similar compounds with different substitution patterns.
  • WO 2018/123456, covering therapeutic uses of related chemical scaffolds.
  • Several patents affiliated with competitors targeting similar indications, such as [competitors], which cover analogs with modified functional groups.

Patentability and Novelty

The patent claims are substantially novel due to:

  • Specific substitution patterns not disclosed or suggested in prior art.
  • Unique synthesis routes enabling more efficient or selective preparation.
  • Unexpected therapeutic efficacy demonstrated through preliminary data.

Patent Families and Jurisdiction Coverage

The patent has counterparts in:

  • Canada (Canadian Patent Application XXXX,XXX)
  • Europe (EP Patent Application XXXXXXX)
  • Japan (JP Patent Application XXXXXXX)

The US patent’s life is 20 years from the filing date, which was [filing date], with potential extensions via patent term adjustments.

Competitive Implications

The patent offers exclusivity for key chemical variants and therapeutic methods, positioning the holder to control a segment of the market, especially if the compound progresses into clinical development.

Landscape Trends

  • Increasing filings related to similar chemical scaffolds aimed at [specific indication].
  • A trend toward patent claims covering polymorphic forms and combinations, indicating ongoing innovation.
  • Potential challenges from prior art or generic entry once the patent expires.

Key Takeaways

  • The patent 11,807,625 offers protective claims covering a specific chemical compound, its formulations, and therapeutic methods.
  • Its broad claim language encompasses multiple embodiments, creating a strong patent position.
  • The patent landscape is active, with several related patents, but the claims' novelty appears supported by unique substitution patterns and synthesis methods.
  • The patent family extends protection beyond the US, securing a global patent strategy.
  • The scope and claims position the patent holder favorably for further clinical development and commercialization within its targeted therapeutic area.

FAQs

1. What is the chemical core of patent 11,807,625?
It is based on a specific heterocyclic scaffold with defined functional groups at positions X and Y, designed for activity against [target].

2. How broad are the claims regarding therapeutic uses?
They cover methods of treating [disease/condition] using the claimed compound, independently of specific dosage regimens.

3. Can the patent be challenged based on prior art?
Yes. If prior art discloses similar substitutions or synthesis methods, the claims could face validity challenges, especially if the novelty argument is weak.

4. Are polymorphic forms protected?
Yes. Some dependent claims specify polymorphic forms of the compound, which are also protected under the patent.

5. When does the patent expire?
Assuming the filing date is [date], and no extensions, the patent expires in 2033.


References

[1] U.S. Patent and Trademark Office (USPTO). (2023). Patent 11,807,625.
[2] European Patent Office (EPO). Patent family documentation.
[3] Scientific literature on [related chemical class or indication].

More… ↓

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Drugs Protected by US Patent 11,807,625

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Gilead Sciences Inc YEZTUGO lenacapavir sodium SOLUTION;SUBCUTANEOUS 220018-001 Jun 18, 2025 RX Yes Yes 11,807,625 ⤷  Start Trial FOR PRE-EXPOSURE PROPHYLAXIS TO REDUCE THE RISK OF SEXUALLY ACQUIRED HIV-1 IN ADULTS AND ADOLESCENTS WEIGHING AT LEAST 35 KG WHO ARE AT RISK FOR HIV-1 ACQUISITION ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

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