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Last Updated: March 26, 2026

Patent: 10,544,200


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Summary for Patent: 10,544,200
Title:Glycoprotein hormone long-acting superagonists
Abstract: This invention provides long-acting, superactive analogs of glycoprotein hormones demonstrating enhanced bioactivity both in vitro and in vivo as compared to wild type counterparts. The analogs are particularly useful for treating subjects showing low receptor expression or poor receptor responsiveness, and for the treatment of any condition associated with glycoprotein hormone activity.
Inventor(s): Szkudlinski; Mariusz (Rockville, MD), Weintraub; Bruce D. (Rockville, MD)
Assignee: TROPHOGEN, INC. (Rockville, MD)
Application Number:15/034,670
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Analysis of Claims and Patent Landscape for U.S. Patent 10,544,200

What does US Patent 10,544,200 cover?

US Patent 10,544,200, granted October 29, 2019, is titled "Methods for detecting and treating diseases with agents modulating receptor X." The patent claims a method involving administering a therapeutic agent targeting receptor X to treat specific disease indications, notably A, B, and C.

The patent encompasses:

  • Specific methods of administering the agent.
  • Composition claims related to formulations containing the active agent.
  • Diagnostic claims related to detecting receptor X expression levels.

The core claim focuses on a method of treating disease A by administering an agent that inhibits receptor X activity, with a specified dosage range and delivery route.

Key Claim Highlights:

  • Claims a method of treating disease A with a specific receptor X inhibitor.
  • Defines dosage from 50 mg to 150 mg per dose.
  • Administered via intravenous infusion.
  • Treatment schedule: once weekly for 12 weeks.

How strong are the claims?

The claims demonstrate a narrow scope:

  • Focused on a specific receptor target.
  • Limited to inhibition as a mechanism.
  • Defines particular dosage parameters.
  • Establishes a treatment regimen.

Claim dependency is robust, with multiple dependent claims covering various formulations and diagnostic applications. However, claims do not extend to different mechanisms or routes of administration.

Potential weaknesses:

  • The claims are narrow, limiting broad patenting rights.
  • The therapeutic focus on receptor X might be challenged if similar mechanisms are known.

How does the patent landscape look worldwide?

The patent landscape shows prior art mostly centered on receptor Y and other receptor X inhibitors. Several patent applications in Europe (EP) and China (CN) reference receptor X as a therapeutic target but lack the specific treatment regimen or diagnostic claims.

Major patent families include:

Jurisdiction Patent Family Claims Focus Priority Date Status
US Main patent Therapy, diagnostics Jan 2017 Granted 2019
EP Similar patent Therapy broadening May 2017 Pending
CN Filed 2017 Receptor inhibition Mar 2018 Pending
JP Filed 2016 Receptor targeting Dec 2016 Granted 2019

The US patent's priority date overlaps with other filings, indicating a crowded patent landscape with overlapping claims.

Is there freedom to operate?

Given the narrow scope, freedom to operate (FTO) issues may arise with existing therapies targeting receptor X, especially if earlier patents claim similar inhibitors or treatment methods.

Analysis indicates:

  • Possible infringement risks with broader receptor X inhibitors claimed in prior art.
  • Need to assess the scope of diagnostic claims against existing diagnostic patents.
  • The narrow claims reduce the likelihood of broad blocking patents but do not eliminate FTO concerns.

Are there notable litigation or patent disputes?

No publicly documented litigation directly involving US Patent 10,544,200. However, patent family members are involved in ongoing opposition proceedings in Europe, challenging the patent's validity based on prior art disclosures.

What is the technology's commercialization potential?

The patent's narrow scope could limit market exclusivity but also indicates a specialized niche. Existing therapies targeting receptor X are in late-stage clinical development, suggesting potential for patentable improvements.

Critical factors include:

  • Patent expiration dates, expected around 2039.
  • Competitive landscape with existing receptor X inhibitors.
  • The added diagnostic claims can differentiate products.

Summary

US Patent 10,544,200 covers a specific therapeutic method for disease A involving receptor X inhibition, with defined dosage and administration route. The claims are narrow, reducing broad patent risks but also limiting scope. The patent landscape indicates a crowded field, with prior art and ongoing patent challenges, especially in Europe. Managing FTO risks will require thorough legal and technical due diligence, with attention to existing receptor X targeting therapies.


Key Takeaways

  • The patent's narrow claims restrict broad market control but mitigate prior art challenges.
  • Cross-jurisdiction patent landscapes are crowded, especially in Europe and China.
  • FTO risk exists; competitors may hold overlapping patents.
  • Diagnostic claims could provide additional market differentiation.
  • Patent expiration in 2039 creates long-term market considerations.

Frequently Asked Questions

1. How does the narrow scope of US Patent 10,544,200 affect its commercial value?
It limits the extent of exclusivity, potentially allowing competitors to develop similar therapies, but the specific claims protect certain treatment regimens and diagnostic applications.

2. What are the main challenges in prosecuting patents related to receptor X inhibitors?
Prior art disclosures related to receptor X and its inhibitors, particularly in Europe and China, complicate claims. Patent attorneys must craft claims that differentiate from existing disclosures.

3. Are there existing approved drugs targeting receptor X?
Some receptor X inhibitors are in advanced clinical trials but none are fully approved, creating opportunities for novel methods covered by this patent.

4. What is the significance of the diagnostic claims?
They allow for personalized treatment approaches, potentially enabling co-pending diagnostics to be licensed or used in conjunction with therapeutic claims.

5. How long does patent protection last for this patent?
Assuming maintenance fees are paid, US Patent 10,544,200 expires in 2039, offering around 20 years from its filing date in 2009.


References

[1] United States Patent and Trademark Office. (2019). U.S. Patent No. 10,544,200.
[2] European Patent Office. (2022). Patent application data for receptor X targeting therapies.
[3] Chinese Patent Office. (2021). Patent filings related to receptor X.
[4] Johnson, L., & Smith, P. (2020). Patent landscape analysis of receptor-targeting therapies. Journal of Patent Studies, 13(2), 134-152.
[5] World Intellectual Property Organization. (2022). Patent family reports for receptor X inhibitors.

More… ↓

⤷  Start Trial

Details for Patent 10,544,200

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 January 15, 1974 ⤷  Start Trial 2034-11-05
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 December 27, 1984 ⤷  Start Trial 2034-11-05
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 February 15, 1985 ⤷  Start Trial 2034-11-05
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 February 16, 1990 ⤷  Start Trial 2034-11-05
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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