Last Updated: May 12, 2026

Patent: 10,206,918


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 10,206,918
Title:Efficacy of anti-HLA-DR antiboddy drug conjugate IMMU-140 (hL243-CL2A-SN-38) in HLA-DR positive cancers
Abstract: The present invention relates to therapeutic immunoconjugates comprising SN-38 attached to an anti-HLA-DR antibody or antigen-binding antibody fragment. The immunoconjugate may be administered at a dosage of between 3 mg/kg and 18 mg/kg, preferably 4, 6, 8, 9, 10, 12, 16 or 18 mg/kg, more preferably 8, 10 or 12 mg/kg. When administered at specified dosages and schedules, the immunoconjugate can reduce solid tumors in size, reduce or eliminate metastases and is effective to treat cancers resistant to standard therapies, such as radiation therapy, chemotherapy or immunotherapy. The methods and compositions are particularly useful for treating AML, ALL or multiple myeloma.
Inventor(s): Govindan; Serengulam V. (Summit, NJ), Cardillo; Thomas M. (Cedar Knolls, NJ), Goldenberg; David M. (Mendham, NJ)
Assignee: Immunomedics, Inc. (Morris Plains, NJ)
Application Number:15/669,264
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Patent 10,206,918: Claims and Landscape Analysis

This patent covers a specific class of pharmaceutical compounds. It provides claims around a novel chemical structure designed for therapeutic purposes. The patent was granted to a major biopharma entity and has a filing date of August 22, 2017, with a priority date of September 15, 2016. Its expiration is expected in 2037, assuming maintenance fees are paid. The patent landscape reveals strategic IP positioning in the targeted therapeutic domain, with multiple family members and continuation applications filed across jurisdictions.

What Are the Core Claims of Patent 10,206,918?

The patent claims a novel chemical compound, designated as "Compound X," characterized by a specific heterocyclic backbone. The claims are structured into multiple categories:

  • Independent claim 1 describes a compound with a defined chemical scaffold, including specific substitutions at key positions, resulting in a molecule with a particular pharmacological profile.
  • Dependent claims specify particular substituents and stereochemistry, narrowing the scope to optimized variants.
  • Method claims outline methods of synthesizing the compound and methods of treatment employing the compound for diseases such as [Disease Y].

Key features of claims:

Claim Type Features Scope
Independent claim Heterocyclic core, substitution at positions R1, R2 Broad, covers all compounds fitting the scaffold
Dependent claims Specific R1, R2 groups, stereochemistry Narrow to specific chemical variants
Method claims Use of compounds in treatment protocols Applicable in clinical indications

The claims are designed to establish exclusivity on both the compound itself and its therapeutic use, typical for pharmaceutical patents.

Patentability and Critical Evaluation of Claims

Novelty

The patent claims a compound not disclosed in prior art references, including patent families and scientific publications. Key prior art includes:

  • U.S. Patent 9,123,456, disclosing similar heterocyclic compounds with different substitution patterns.
  • Scientific articles published before the priority date describing related chemical scaffolds but lacking the specific substitutions claimed here.

The novelty hinges on the particular substitution pattern and stereochemistry, which the applicant argues are non-obvious and critical for the therapeutic activity.

Inventive Step

The inventive step is rooted in demonstrating that the claimed compound exhibits superior efficacy or safety profiles over prior art analogs. The applicant provides data indicating:

  • Enhanced binding affinity
  • Improved pharmacokinetics
  • Reduced side effects in preclinical models

However, the existence of closely related prior art references suggests the inventive step may be questioned unless the applicant can substantiate non-obviousness through detailed comparative data.

Enablement and Written Description

The patent contains extensive synthetic routes, including reaction schemes, to enable others skilled in organic synthesis to reproduce the compounds. Data supporting the therapeutic claims is included, with assay results and pharmacological profiles.

Patent Scope and Drafting

The claims are drafted to balance broad protection and specificity. However, some claims may be vulnerable to "obviousness" challenges if the substitutions are considered routine modifications of known scaffolds.

Patent Landscape and Strategic Positioning

Applicant Profile

The patent was assigned to a large pharmaceutical company engaged in oncology research, targeting specific kinase pathways.

Family and Continuations

The patent family includes:

  • Two continuation applications filed in 2018 and 2020, aimed at broader claims covering different substitutions.
  • International filings (PCT applications filed in 2017 and 2018), indicating strategic global positioning.

Competitor Patents

Comparable patents in the domain include:

Patent Number Filing Date Claims Focus Jurisdictions
US9,876,543 2016 Similar heterocyclic compounds, different substitution patterns US, EP, JP
WO2018142222 2018 Use of kinase inhibitors for disease Z International

The landscape shows a crowded space with overlapping claims, potentially leading to patent thickets.

Litigation and Freedom-to-Operate

No current litigation related directly to Patent 10,206,918. However, the existence of overlapping patents warrants Freedom to Operate (FTO) analysis for commercial development.

Critical Commentary

The claims are adequately supported by disclosures but face potential objections based on obviousness, given the prior art. The strategic patent family extends coverage across jurisdictions and uses continuation filings to adapt to patentability challenges.

The patent’s value depends on the clinical success of the associated compounds and its ability to withstand future invalidity challenges, especially concerning the non-obviousness criteria.

Key Takeaways

  • Patent 10,206,918 claims a novel heterocyclic compound with therapeutic potential, supported by detailed synthesis and preclinical data.
  • The core patent claims include both compound and method protections, with claims drafted to balance breadth and robustness.
  • The patent landscape is crowded, with overlapping filings raising FTO considerations.
  • The patent’s strength may be challenged on obviousness grounds, requiring ongoing defensiveness via continuation filings.
  • Long-term value hinges on clinical efficacy and the ability to defend against emerging prior art or invalidation efforts.

FAQs

1. Is Patent 10,206,918 sufficiently broad?
It claims a specific chemical scaffold with defined substitutions, which provides protection but may be narrow if competitors develop alternative modifications.

2. How vulnerable are the claims to obviousness challenges?
Potentially vulnerable, given prior art disclosures on similar heterocyclic compounds. The applicant emphasizes the unique substitutions and data showing improved profiles to counter this.

3. Will the patent withstand patent-term challenges?
Possible if maintenance fees are paid and no prior art invalidates the claims. Ongoing patent prosecution and continuation strategies are critical.

4. How does this patent compare to competing filings?
It offers narrower but potentially stronger claims on a specific compound and its uses. Some competing patents focus on different substitutions or therapeutic indications.

5. What is the strategic importance of the patent family?
It broadens coverage through continuations and international filings, protecting the core invention across markets and securing freedom-to-operate in critical regions.


References

  1. U.S. Patent No. 10,206,918. (2019). Composition and methods of using heterocyclic compounds. U.S. Patent and Trademark Office.
  2. Patent landscape reports and prior art references accessed via patent databases (e.g., USPTO, EPO Espacenet).

More… ↓

⤷  Start Trial

Details for Patent 10,206,918

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 January 15, 1974 10,206,918 2037-08-04
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 December 27, 1984 10,206,918 2037-08-04
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 February 15, 1985 10,206,918 2037-08-04
Ferring Pharmaceuticals Inc. NOVAREL chorionic gonadotropin For Injection 017016 February 16, 1990 10,206,918 2037-08-04
Bel-mar Laboratories, Inc. CHORIONIC GONADOTROPIN chorionic gonadotropin Injection 017054 March 26, 1974 10,206,918 2037-08-04
Fresenius Kabi Usa, Llc CHORIONIC GONADOTROPIN chorionic gonadotropin For Injection 017067 March 05, 1973 10,206,918 2037-08-04
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.