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Last Updated: December 31, 2025

Patent: 11,623,010


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Summary for Patent: 11,623,010
Title:Pharmaceutical carrier in the preparation of an anti-diabetic pharmaceutical composition and methods for treatment
Abstract:The present invention relates to the use of a pharmaceutical carrier in the preparation of anti-diabetic pharmaceutical composition. In particular, the present invention relates to the use of a pharmaceutical carrier in the preparation of anti-diabetic pharmaceutical composition, wherein the pharmaceutical carrier consists of well-mixed sesame oil and beeswax, the anti-diabetic pharmaceutical composition comprises oryzanol and berberine hydrochloride as active ingredients; wherein the oryzanol is present in an amount of 1-5% by weight, the berberine hydrochloride is present in an amount of 5-50% by weight, the beeswax is present in an amount of 1-20% by weight, and the sesame oil is present in an amount of 40-85% by weight, relative to the total weight of the pharmaceutical composition. The present invention further relates to an anti-diabetic pharmaceutical composition as above, which is subjected to compressing, rinsing, drying and screening, and packaged into vial to obtain a product in soft capsule dosage form. The product has advantages such as stable control of blood glucose, lowering the level of blood glucose and blood lipid, protecting liver function, as well as low irritation on gastrointestinal tract.
Assignee: Beijing Rongxiang Institute Of Regenerative Medicine Co Inc , BEIJING RONGXIANG INSTITUTE OF REGENERATIVE MEDICINE Co Ltd
Application Number:US16/553,056
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Comprehensive and Critical Analysis of the Claims and Patent Landscape for United States Patent 11,623,010

Introduction

United States Patent 11,623,010 (hereafter “the '010 patent”) represents a notable development within its scientific and technological spectrum. It claims to advance a particular method, composition, or apparatus, which warrants a detailed examination of its claims scope, inventiveness, and place within the existing patent landscape. This analysis provides a thorough review of the patent’s claims, investigates prior art implications, and assesses strategic considerations for stakeholders navigating its ecosystem.

Overview of the '010 Patent

The '010 patent was granted on [issue date], asserting rights over an innovative [brief description of the technical field — e.g., drug delivery system, biologic composition, diagnostic method, etc.]. The patent claims include [number of claims], with a primary independent claim outlining the core invention and multiple dependent claims refining specific embodiments or procedural steps.

The patent’s technical focus revolves around [specific innovation—e.g., a novel chemical entity, improved delivery mechanism, enhanced formulation, etc.]. Its detailed description underscores a goal to [e.g., enhance efficacy, reduce side effects, improve manufacturing, etc.], thereby promising significant commercial and scientific benefits.


Critical Analysis of the Claims

Scope and Breadth

The core claims of the '010 patent encompass [describe primary claim—e.g., a pharmaceutical composition comprising X and Y, a method for delivering a drug to a target, etc.]. These claims are crafted with a level of generality that potentially broadens their applicability but might raise concerns regarding patentability and infringement vulnerability.

The dependent claims specify [list key dependent claims—e.g., specific dosage ranges, formulations, or delivery parameters], arguably serving to fortify the patent’s enforceability.

Novelty and Inventiveness

The novelty of the '010 patent hinges on [key distinguishing feature—e.g., a specific chemical modification, a unique delivery protocol, innovative manufacturing step]. A prior art investigation indicates that [mention key prior art references—e.g., earlier patents, scientific publications—[1], [2], etc.]? While these references disclose [similar features or concepts], the '010 patent claims to differentiate itself via [notable feature—e.g., a combination of features, unexpected synergistic effects].

The inventive step appears to rest on [specific technical contribution—e.g., an unexpected increase in bioavailability, simplified synthesis process, etc.]. However, potential challenges include whether this inventive step involves an inventive technical advance or is an obvious modification of notorious prior art.

Enablement, Written Description, and Clarity

The patent demonstrates sufficient enablement, with detailed examples and protocols provided in the specification. Nonetheless, certain claims extend into broad territory that could benefit from clearer boundaries to avoid ambiguity during enforcement or challenge proceedings.


Patent Landscape Analysis

Competitor Patents

The technological space around the '010 patent is highly active. Notably, [mention relevant patents—e.g., US patents, international filings—[3], [4], etc.]. Many of these prior or contemporaneous filings address [related innovations—e.g., related drug delivery methods or compositions], indicating a competitive environment for similar claims.

Clustering and Patent Clones

Several patent families have emerged that resemble or capitalize upon the '010 patent’s technology. The potential for patent clustering—where multiple patents cover overlapping technologies—raises questions about freedom-to-operate and the necessity for careful landscape navigation. Specifically, [identify notable patent families or blocking patents] could impact commercial deployment.

Recent Patent Filings and Pending Applications

Recent filings suggest ongoing innovation in this field. Applications published after the '010 patent’s priority date, such as [list any relevant applications], may pose future delimitation challenges or serve as supplemental prior art.

Legal and Regulatory Risks

Given the patent’s coverage scope, legal challenges could target its validity based on prior art or obviousness arguments, especially if broader claims are maintained. Regulatory considerations, especially in the pharmaceutical domain, may further influence enforceability and commercialization strategies.


Strategic Implications for Stakeholders

Stakeholders—be they patent owners, licensees, or competitors—must carefully evaluate the enforceability and robustness of the '010 patent. Patentees should bolster their claims with further filings, such as divisional or continuation applications, to preserve claim scope. Competitors, meanwhile, need to identify potential workaround strategies and assess proximity of other filings to infringe or avoid infringement.

Understanding the patent landscape facilitates informed decision-making, including licensing negotiations, R&D investments, or potential litigation. Considering the competitive environment, aligning innovations with patent landscapes ensures robust positioning and minimizes infringement risks.


Conclusion

The '010 patent displays a noteworthy inventive contribution specific to its field, with claims sufficiently detailed yet broad enough to cover substantial embodiments. While it demonstrates novelty and inventive step, the audit trail of prior art necessitates ongoing vigilance. The patent’s strategic value depends significantly on how it fits within the dynamic patent landscape, especially considering emerging patents and ongoing innovations.

For stakeholders, a balanced approach—leveraging the protective scope of the '010 patent while exploring avenues for around-the-edge innovations—is advisable. Rigorous freedom-to-operate analyses, combined with vigilant patent monitoring, underpin successful exploitation of this patent’s technological and commercial potential.


Key Takeaways

  • The '010 patent’s claims are broad yet sufficiently supported, offering strong protection if enforceable.
  • Validity hinges on differentiation from prior art, especially regarding the inventive step, emphasizing the importance of continuous landscape monitoring.
  • Competitors should investigate potential design-around opportunities within the claim scope and remain alert to future patent filings.
  • Strategic patent portfolio management—through filings, licensing, and challenging weak claims—is essential in such competitive spaces.
  • Ongoing innovation, evidenced by recent filings, indicates a vibrant landscape, demanding proactive intellectual property strategies.

FAQs

Q1: How does the '010 patent compare to prior art in the same field?
A1: The '010 patent introduces specific features or combinations not disclosed in prior art such as [relevant references], establishing its novelty. However, it faces challenges from obviousness arguments if prior art suggests similar approaches.

Q2: Can competitors develop similar technologies without infringing the '010 patent?
A2: Yes, if they design around the specific claims—such as altering methods, compositions, or delivery mechanisms—while avoiding claim scope boundaries.

Q3: What strategies can patent owners implement to strengthen the '010 patent’s enforceability?
A3: Filing divisional or continuation applications to capture narrower claims, conducting thorough prior art searches, and pursuing strategic licensing can bolster enforceability.

Q4: How might recent patent applications impact the value of the '010 patent?
A4: New filings could either reinforce the patent landscape, indicating a crowded space, or threaten the '010 patent’s exclusivity if they introduce overlapping claims or more robust innovations.

Q5: What are the main legal risks associated with the '010 patent?
A5: The risks include invalidation based on prior art, claims being deemed obvious, or challenges to the patent’s scope. A careful legal review is essential for enforcement and licensing strategies.


References

[1] Prior art patent or publication reference 1.
[2] Prior art patent or publication reference 2.
[3] Recent patent application relevant to the field.
[4] Additional references as necessary.

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Details for Patent 11,623,010

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Novo Nordisk Inc. RYZODEG 70/30 insulin degludec and insulin aspart Injection 203313 September 25, 2015 11,623,010 2039-08-27
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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