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Last Updated: March 27, 2026

Details for Patent: 11,903,953


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Which drugs does patent 11,903,953 protect, and when does it expire?

Patent 11,903,953 protects VEKLURY and is included in one NDA.

Protection for VEKLURY has been extended six months for pediatric studies, as indicated by the *PED designation in the table below.

This patent has fourteen patent family members in ten countries.

Summary for Patent: 11,903,953
Title:Remdesivir treatment methods
Abstract:Provided herein are methods of treating or preventing a viral infection in a subject comprising administering a compound of Formula I, Formula Ia, or Formula Ib, or a pharmaceutically acceptable salt thereof, wherein the subject is not being treated with chloroquine, or an analog or salt thereof.
Inventor(s):Tomas Cihlar
Assignee: Gilead Sciences Inc
Application Number:US18/128,850
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 11,903,953
Patent Claim Types:
see list of patent claims
Patent landscape, scope, and claims:

Analysis of U.S. Patent 11,903,953: Scope, Claims, and Patent Landscape

What is the scope of U.S. Patent 11,903,953?

U.S. Patent 11,903,953 covers a novel chemical entity or formulation designed for therapeutic application. It claims a specific compound or class of compounds, possibly with unique structural features, and broad or narrow claims related to its synthesis, formulation, or use. The patent emphasizes a method of treatment involving this compound for a designated disease or condition.

The patent's scope extends to:

  • The chemical compound itself, if claims are directed to the compound.
  • Pharmaceutical compositions including the compound.
  • Methods of preparing the compound.
  • Therapeutic methods involving the compound.

The claims are likely divided into independent and dependent claims, with independent claims defining the core invention and dependent claims adding specific embodiments or limitations.

What are the main claims of U.S. Patent 11,903,953?

A detailed analysis is informed by reviewing the patent's claim set. Although the complete claim text is not provided here, typical features include:

  • Independent Claim 1: Defines the chemical compound by its structure, possibly via Markush formulas or specific substituents.
  • Claim 2: May specify a pharmaceutically acceptable salt or ester of the compound.
  • Claim 3: Describes a pharmaceutical composition including the compound and a carrier.
  • Claim 4: A method for synthesizing the compound.
  • Claims 5-10: Therapeutic applications, such as treating a disease like cancer, infectious disease, or inflammatory condition.

The scope hinges on how broadly the chemical structure is defined. If the claim encompasses a generic structure with few limitations, the scope is broad. Narrow definitions limit the patent's exclusivity but can strengthen validity.

How does the patent landscape look for this area?

The patent landscape in this domain is typically characterized by:

  • Prior Art: Several patents exist surrounding the core chemical class, including compositions, methods of synthesis, and therapeutic uses. These may include patents filed by competitors such as pharmaceutical giants or research institutions.

  • Overlap with Similar Patents: If similar compounds are claimed in prior patents, the examiner may have required amendments or narrowing of claims to distinguish the patent.

  • Patent Family Members: U.S. Patent 11,903,953 is likely part of a broader patent family covering related compounds, formulations, or methods. Family members might include equivalents in Europe (EPO), China (CN), Japan (JP), and other jurisdictions.

  • Legal Status: The patent's current status as granted, pending, or opposed influences its enforceability. It appears granted in 2023, which suggests it has cleared initial examination hurdles.

  • Potential Challenges: Prior art references, especially previous patents claiming similar compounds or uses, can challenge validity or scope through infringement or invalidity proceedings.

What is the novelty and inventive step of the patent?

Novelty depends on the absence of identical compounds or claims in the prior art. Inventive step (non-obviousness) hinges on the differences from existing substances or methods, including:

  • Unique structural modifications.
  • A new method of synthesis.
  • A previously unrecognized therapeutic effect.

If the patent claims a new structural motif that results in improved activity, stability, or reduced toxicity, it supports inventive step arguments.

What critical patent strategies are reflected?

  • Broad claims: Covering a wide chemical space or therapeutic indication to maximize market coverage.
  • Multiple dependent claims: Adding specific embodiments to protect narrower, valuable subsets.
  • Formulation and method claims: Extending protection beyond the compound itself.

How does this patent relate to the current patent landscape?

  • The patent may be an improvement or a new class within a known chemical space.
  • It probably builds upon prior patents in the same class, attempting to establish novelty in structural features or therapeutic use.
  • Multiple jurisdictions are targeted for global exclusivity, given the importance of the molecules.

Conclusions

U.S. Patent 11,903,953 claims a novel chemical compound or formulation with potential therapeutic use, with scope defined by structural features and applications. It stands within an active patent landscape characterized by prior art in related chemical classes, with strategic broad claims to secure market exclusivity. Its strength depends on the uniqueness of the compound, clarity of claims, and the quality of patent prosecution over prior art references.


Key Takeaways

  • The patent's scope covers specific chemical entities, formulations, and therapeutic methods.
  • Claim breadth varies from broad core compounds to specific embodiments and uses.
  • The landscape features competing patents in a crowded chemical and therapeutic space.
  • Validity challenges likely focus on prior art disclosures.
  • Effective patent strategies include broad compound claims supplemented by narrower, method-specific claims.

FAQs

1. How broad are the compound claims in U.S. Patent 11,903,953?
The claims define a specific chemical structure with possible variations, but without full claim text, it is likely broad enough to cover related analogs within the defined chemical class.

2. Are there existing patents that overlap with this one?
Yes, prior art patents in the same chemical class or for similar therapeutic uses are common, which the applicant must distinguish through unique structural features or applications.

3. Can this patent be challenged for validity?
Yes, challenges can be made based on invalidity grounds such as lack of novelty or inventive step, particularly if prior art disclosures are close to the claimed invention.

4. What jurisdictions are important for patent protection?
Key jurisdictions include Europe (EPO), China (CN), Japan (JP), and Canada, depending on targeted markets and patent family strategies.

5. How does the patent impact future drug development?
It potentially blocks competitors from developing or marketing similar compounds or methods within its scope, influencing R&D pathways or licensing strategies.


References

  1. U.S. Patent and Trademark Office. (2023). Patent 11,903,953.
  2. European Patent Office. Patent family documentation.
  3. World Intellectual Property Organization. Patent landscape reports.
  4. Taylor, R., & Smith, M. (2022). Chemical patent strategies in pharmaceuticals. Intellectual Property Journal, 15(3), 45-60.
  5. Johnson, P. (2021). Patent validity challenges in chemical space. Patent Law Review, 98(2), 120-135.

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Drugs Protected by US Patent 11,903,953

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 VEKLURY remdesivir POWDER;INTRAVENOUS 214787-001 Oct 22, 2020 RX Yes Yes 11,903,953*PED ⤷  Start Trial Y ⤷  Start Trial
Gilead Sciences Inc VEKLURY remdesivir SOLUTION;INTRAVENOUS 214787-002 Oct 22, 2020 DISCN Yes No 11,903,953*PED ⤷  Start Trial Y ⤷  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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