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Fc Engineering Patents: Leaders, Trends & White Space 2026

Fc Engineering Patents: Leaders, Trends & White Space 2026
https://www.patsnap.com/resources/blog/rd-blog/fc-engineering-and-effector-function-patent-landscape/ · Patsnap · data cut-off 2026-07-31 · downloaded from the live page
Patent Landscape · Antibody Engineering
Fc Engineering and Effector Function Patents
  • 29.1% concentration. The five leading assignees hold 19,775 of the 67,903 records in scope — a genuinely top-heavy field for a therapeutic antibody sub-domain.
  • Filings cooled from a 2021 peak. Volume ran from 1,636 records in 2021 to 985 in 2024, a 40% pullback over that span, though 2025-26 figures are still filling in as publications lag filing.
  • Two of the five most-cited documents are pre-2000 filings. US6737056B1 and US5648260A still anchor effector-function claim language two decades on, a sign of how much foundational IP underlies current designs.
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67.9K
Published Records
29%
Top-5 Share of All Records
-40%
Filing Growth 2021→2024
US
Leading Jurisdiction

Filing growth compares 2021 (1,636 records) with 2024 (985) — a three-year span. 2024 is the most recent year we treat as complete: publication lags filing by roughly 18 months, so 2025 onwards are still filling in and any growth rate that ends there would understate the field. Top-5 share is the combined record count of the five largest assignees divided by all 67,903 records in scope (CR5), not by the ranked leaders only.

Published byPatsnap Research··7 min readSourced from Patsnap Eureka
Overview

What this landscape covers

Fc engineering spans the amino-acid, glycan and receptor-binding modifications that tune how an antibody’s constant region interacts with Fc receptors and complement. This landscape pulls records that combine core concepts — Fc engineering, effector function, neonatal Fc receptor — with the specific mechanisms used to deliver them: afucosylation, complement activation, half-life extension, silenced Fc variants, glycan profiling and receptor binding assays. The scope therefore captures both the biology (what the modification does to ADCC, ADCP or CDC) and the engineering route (how the modification is made and measured).

67,903 published records sit in scope, spanning filings from 2015 through the 2026-07-31 cut-off. Because publication trails filing by roughly 18 months, the most recent one to two years understate real filing activity and should be read as provisional.

Filing activity and technology composition, 2015 to date
  1. 1GENENTECH INC11,107
  2. 2F HOFFMANN LA ROCHE & CO AG5,086
  3. 3GENMAB AS1,419
  4. 4AMGEN INC1,170
  5. 5MACROGENICS INC993
  6. 6OMEROS CORP882
  7. 7AMGEN RESEARCH (MUNICH) GMBH879
  8. 8F HOFFMANN LA ROCHE INC873
  9. 9CHUGAI PHARMA CO LTD853
  10. 10ALEXION PHARMACEUTICALS INC825
Source: Patsnap Eureka. Assignee ranking and totals. Derived from a Patsnap search on Fc Engineering and Effector Function covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.Run this in Eureka MCP

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The data

Filing trend and technology composition

Two views of the same 67,903-record corpus: how filing volume has moved year over year, and which IPC subclasses carry the claim density.

Filing trend: a 2021 peak, then a pullback

Annual filings rose to a peak of 1,636 records in 2021, then eased to 985 by 2024 — a 40% decline over that three-year window. 2017 opened the tracked window at 1,124 records; years from 2025 onward are still incomplete because of publication lag and should not be read as a continued fall.

Filing trend: a 2021 peak, then a pullback05001,0001,5002,0001,12420172018201920201,63620212022202320242025782026Most recent year is partial — publication lag means later filings are not yet visible.

Where the claims sit: peptide chemistry and formulation dominate

C07K (peptides and proteins) covers 25.6% of the 67,903 records, ahead of A61K (medicinal preparations) at 19.4% and A61P (therapeutic activity) at 12.8%. Downstream production and analysis classes — C12N, G01N, C12P — sit in the single digits, suggesting the field's claim pressure is concentrated on the molecule itself rather than on manufacture or assay method, which is where openings tend to sit.

Where the claims sit: peptide chemistry and formulation dominateC07K · Peptides & proteins17,41725.6%A61K · Medicinal preparations13,15019.4%A61P · Therapeutic activity of compou…8,70012.8%C12N · Microorganisms & genetic engin…3,8935.7%G01N · Material analysis & testing2,2643.3%C12P · Fermentation & enzymatic synth…1,4682.2%C12Q · Measuring & testing involving …5100.8%C07H · Sugars & nucleic acids4900.7%Other7871.2%

Shares are the percentage of the 67,903 records in scope. A patent can carry several IPC classes, so the shares add up to more than 100%.

Source: Patsnap Eureka. Filing trend and technology composition. Derived from a Patsnap search on Fc Engineering and Effector Function covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.

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Key patents

The documents anchoring this field

Representative filing
US7790858B22010-09-07

US7790858B2 — Polypeptide variants with altered effector function

GENENTECH, INC.

The present invention concerns polypeptides comprising a variant Fc region. More particularly, the present invention concerns Fc region-containing polypeptides that have altered effector function as a consequence of one or more amino acid modifications in the Fc region thereof.Filed by Genentech, granted 2010-09-07 — part of a family that includes several of the field's most-cited prior documents.

US7790858B2 — patent drawing 1US7790858B2 — patent drawing 2
View full record
Most-cited records in scope
#Publication no.Patent titleCitations
1US6737056B1Polypeptide variants with altered effector function7,652
2US5648260ADNA encoding antibodies with altered effector functions7,516
3US6194551B1Polypeptide variants6,894
4WO2000042072A2Polypeptide variants with altered effector function4,987
5WO1999051642A1Antibody variants and fragments thereof4,771
6US20030157108A1Glycoprotein compositions4,087
7US6982321B2Altered antibodies3,434
8US7332581B2Polypeptide variants with altered effector function3,101
9WO2010077634A1Anti-PD-l1 antibodies and their use to enhance t-cell function2,970
10US20050123546A1Antigen binding molecules with increased Fc receptor binding affinity and effector function2,849

Citation counts reflect an older, foundational skew: pre-2010 filings accumulate citations simply by being available longer, so treat this as a map of influence, not of current claim strength.

Each row carries its publication number; clicking a row searches Eureka by that number.

Source: Patsnap Eureka. Citation counts and representative records. Derived from a Patsnap search on Fc Engineering and Effector Function covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.Run this in Eureka MCP
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Insights

What the numbers mean for a filing decision

Three read-throughs from the concentration, trend and citation data above.

Concentration
29.1%
of 67,903 records held by top 5

A top-heavy field, but not a closed one

The five leading assignees hold 29.1% of the 67,903 records in scope, and the top ten extend that to 35.5%. That leaves the majority of filings spread across a long tail of single- and few-filing entrants, so freedom-to-operate work still needs to check well past the household names.

Top 5: 19,775 records · Top 10: 24,087 records
Momentum
-40%
2021 to 2024 filing change

Volume has eased from its 2021 high, not collapsed

Filings ran from 1,636 records at the 2021 peak to 985 in 2024. Several of the most active assignees also show sharp year-on-year drops in the latest tracked year, but that year is still filling in under publication lag, so read the direction rather than the exact percentage.

2021 peak: 1,636 records · 2024: 985 records
Claim density
25.6%
of records classed under C07K

Molecule-level claims crowd out process claims

C07K and A61K together touch close to half of all records once overlap is accounted for, while assay and production classes (G01N, C12P, C12Q) sit under 4% each. That imbalance is where less-contested claim territory tends to sit — in how a variant is made or measured rather than in the variant itself.

C07K 25.6% · A61K 19.4% · G01N 3.3%
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Eureka can read the same corpus for gaps instead of for coverage: under-claimed branches adjacent to fc engineering and effector function, with the prior art for and against each one.

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Source: Patsnap Eureka. Co-assignee relationships and derived observations. Derived from a Patsnap search on Fc Engineering and Effector Function covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.Run this in Eureka MCP
Players

Who is filing, and where the activity is slowing

The ranked leaders span both large-molecule originators and specialist antibody-engineering houses. Recent-year momentum figures should be read with the same publication-lag caveat as the overall trend: a steep year-on-year drop in the latest tracked year is partly an artefact of records not yet published.

Leader
11,107
records

A single assignee well ahead of the field

The leading assignee holds 11,107 records, well clear of fifth place at 993 and tenth place at 825 — a gap that says more about filing volume over a decade than about any single blocking patent.

Leader vs. 5th: 11,107 vs. 993
Mid-field
993 → 825
5th to 10th place

A tight band from fifth to tenth

The drop from fifth place (993 records) to tenth (825) is far shallower than the drop from first to fifth, indicating a genuine mid-tier of comparably active filers rather than a sharp cliff after the leader.

Top 10 combined: 24,087 records
Collaboration
389
strongest co-assignee pairing

Co-filing concentrates around a handful of pairs

Ten co-assignee pairs recur across the corpus, with the strongest pairing appearing 389 times and the next two above 200 — evidence of durable, structured research partnerships rather than one-off joint filings.

10 recurring co-assignee pairs identified
🔍
Under-claimed sub-areas worth checking before filing
Process, assay and combination claims sit well below the molecule-level classes in filing density.
Fc silencing variant assay methodsGlycan profiling analytics for afucosylation QCFcRn-mediated half-life extension in non-IgG scaffoldsComplement activation potency assaysCombination Fc-silenced bispecific formats
Rank all filers by momentum →
Recent-year filing momentum by assignee
AssigneeRecent yearYoY
Genentech, Inc.7-89%
F. Hoffmann-La Roche Ltd7-50%
Alexion Pharmaceuticals, Inc.5-62%
F. Hoffmann-La Roche AG4-90%
Omeros Corporation2-50%
Chugai Pharmaceutical Co., Ltd.2-78%
Genmab A/S2-83%
Xencor, Inc.1-93%
Source: Patsnap Eureka. Assignee-level momentum. Derived from a Patsnap search on Fc Engineering and Effector Function covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.Run this in Eureka MCP
What's next

Where to take this from here

The landscape points to specific next checks rather than a single conclusion.

Check freedom-to-operate against the long tail

With 70.9% of records held outside the top five assignees, a clearance search needs to extend well past the obvious originators into the long tail of few-filing entrants.

Run a freedom-to-operate check in Eureka →

Map the under-claimed process classes

Assay, production and measurement classes carry far less claim density than the molecule classes. That gap is worth mapping in detail before committing to a filing strategy.

Explore white space in Eureka →

Track momentum, not just totals

Recent-year drops across several leading assignees may reflect publication lag as much as a real slowdown. Re-checking this trend in a future data cut will separate the two.

Set up a monitoring search in Eureka →
Source: Patsnap Eureka. Forward-looking reading of the same dataset. Derived from a Patsnap search on Fc Engineering and Effector Function covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.Run this in Eureka MCP
FAQ

Common questions on Fc engineering patents

Answers are grounded in the same dataset. Derived from a Patsnap search on Fc Engineering and Effector Function covering 2015–2026, data cut-off 2026-07-31. Counts reflect published records only and shift as new filings publish.Run this in Eureka MCP

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Disclaimer. This page is generated from Patsnap Eureka data drawn from a limited snapshot of global patent and scientific-literature records, and is provided for general information and reference only.

Patent data carries inherent limitations: recent filings (typically the most recent 18–24 months) are under-counted due to standard publication lag; counts may be reported at either a patent-family or a patent-record basis and are not always directly comparable; classification, applicant-name, and citation data may contain errors, duplicates, or omissions; and the underlying search query defines and constrains the scope shown. As a result, the analysis may be incomplete or inaccurate and may not reflect the full technology landscape.

Nothing on this page constitutes an exhaustive prior-art, novelty, freedom-to-operate, or validity search, nor does it constitute legal, financial, investment, or professional advice, and it should not be relied upon as such. Any patent, commercial, or strategic decision should be verified independently and reviewed with qualified patent, legal, and domain professionals. Patsnap makes no warranties, express or implied, as to the accuracy, completeness, or fitness for any particular purpose of the information presented.

Machine translation. Assignee and organisation names originally recorded in Chinese, Japanese or Korean have been rendered into English by an AI translation step so that the tables stay readable. These renderings are best-effort and may not match a company’s registered English name; the original name is what the underlying patent record carries, and it is what any Eureka query launched from this page uses.

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