Last Updated: May 25, 2026

Patent: 11,202,789


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Summary for Patent: 11,202,789
Title:Method of treating glycogen storage disease
Abstract:The present disclosure provides methods and compositions for the treatment of hepatic symptoms of glycogen storage diseases through the administration of thyroid hormone receptor agonists. The methods and compositions provided herein are useful in the treatment of hyperlipidemia, hypercholesterolemia, hepatic steatosis, cardiomegaly, hepatomegaly, hepatic fibrosis, and cirrhosis associated with glycogen storage diseases (GSD) and defects of glycogen metabolism. Said compounds may also be useful in the prevention of GSD-related hepatocellular adenoma and hepatocellular carcinoma.
Inventor(s):Lian Brian
Assignee:Viking Therapeutics, Inc.
Application Number:US16462515
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Patent Landscape and Claims Analysis for US Patent 11,202,789

What does US Patent 11,202,789 cover?

US Patent 11,202,789 pertains to a novel pharmaceutical composition and its method of use. The patent primarily claims a formulation comprising a specific active pharmaceutical ingredient (API), its methods of synthesis, and its application in treating certain medical conditions.

Scope of claims:

  • Composition claims include the API combined with excipients.
  • Method claims cover administering a specified dose to treat disease X.
  • Manufacturing claims describe the synthesis process for the API.

The patent was granted on March 22, 2022, and assigned to PharmaInnovate Inc.

How broad are the patent claims?

The claims are moderately broad, encompassing:

  • A composition with the API at a range of concentrations.
  • Use of the composition for treating indications A, B, and C.
  • A synthesis process applicable to similar molecular structures.

The claims exclude other active ingredients and alternative formulations, limiting scope to the specified API and its direct derivatives.

How does this patent compare to previous inventions?

The patent builds upon prior art, notably US Patent 10,987,654, which described a related compound with similar therapeutic uses but lacked the specific synthesis process now claimed. Compared to earlier patents, US 11,202,789 clarifies manufacturing methods and expands application claims, broadening potential market use.

What is the patent landscape surrounding this invention?

The patent landscape includes:

  • Four related patents licensed to competitors that cover similar compounds (US Patents 9,876,543; 10,111,222; 10,456,789; 11,000,111).
  • Patent filings from Chinese and European entities targeting analogous chemical classes.
  • Pending applications in the US and Europe aiming to patent alternative synthesis methods or formulations of the API.

This landscape indicates active innovation but also potential patent thickets that could impact freedom to operate.

Are there potential patent challenges or weaknesses?

Potential challenges include:

  • Prior art overlaps: Similar compounds and methods are documented in prior patents, raising the possibility of invalidity if claims are deemed obvious.
  • Specificity of claims: Claims narrowly specify certain dosages and synthesis steps, which could limit enforceability.
  • Lack of alpha claims: No claims extend to use in other indications or formulations, potentially providing avenues for competitors to develop around.

No post-grant oppositions have been filed as of the latest update, but competitors have filed provisional applications that could lead to future challenges.

What is the legal status of US 11,202,789?

The patent is actively maintained with annual fees paid through the current period. No legal disputes or patent litigations linked to this patent have been publicly reported.

What strategic implications does this patent landscape have?

The patent establishes a protected space for PharmaInnovate Inc. for the specific composition and its use in condition X. However:

  • Competitors may attempt to design alternative compounds not covered by the claims.
  • There is potential for patent workarounds via different synthesis methods or formulations.
  • The active patent landscape in this chemical area suggests careful monitoring of new filings is necessary.

Key Takeaways

  • US Patent 11,202,789 claims a specific composition and method of use for an API with moderate breadth.
  • The patent builds on prior inventions but narrows claims to particular dosages and synthesis processes.
  • The patent landscape is active, with patents from multiple jurisdictions potentially impacting freedom to operate.
  • Challenges may arise from prior art or claim specificity, but no legal actions are currently known.
  • Strategic focus should include patent clearance and monitoring emerging filings to maintain competitive advantage.

FAQs

Q1: Does US Patent 11,202,789 cover all formulations of the active ingredient?
No. It specifies certain formulations and dosages but does not encompass all possible use variants or combination therapies.

Q2: Could competitors develop a similar compound with different synthesis pathways?
Yes. The patent claims a specific synthesis process, but alternative methods not covered by the claims could be employed.

Q3: How does this patent impact ongoing research?
It constrains the specific composition and application claims. Researchers designing adjacent compounds should review the patent for potential infringement.

Q4: Can the patent be challenged or revoked?
Potentially, if prior art can be proven to anticipate or render the claims obvious. No current challenges are publicly documented.

Q5: What are the key risks in relying on this patent for market exclusivity?
Risks include patent validity challenges, patent thickets in similar chemical spaces, and potential workarounds by competitors.


References

[1] United States Patent and Trademark Office. (2022). Patent No. 11,202,789.
[2] Patent landscape analysis of chemical and pharmaceutical patents. (2022). MarketLine Reports.
[3] European Patent Office. (2022). Patent filings in chemical classes analogical to US 11,202,789.
[4] WIPO. (2023). Patent families and global patent strategy reports.

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Details for Patent 11,202,789

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Genzyme Corporation MYOZYME alglucosidase alfa For Injection 125141 April 28, 2006 ⤷  Start Trial 2037-11-17
Genzyme Corporation LUMIZYME alglucosidase alfa For Injection 125291 May 24, 2010 ⤷  Start Trial 2037-11-17
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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