Eureka on the web
When you want the answer in the next five minutes.
The agent works the prompt against patents and technical literature, citing every source.
Run your analysis now →Filing growth compares 2021 (43 records) with 2024 (28) — 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 1,039 records in scope (CR5), not by the ranked leaders only.
Harvest timing decisions in mammalian cell culture sit at the intersection of process control and product quality: when a manufacturer pulls a batch determines titer, impurity load and the viability profile of the cells doing the producing. This landscape tracks patents and applications that combine cell culture process claims with signals used to decide when to stop a run — viability decline, apoptosis markers, product titer and impurity release — filed under the core cell-culture and bioreactor classification codes.
The 1,039 records in scope span 2015 through the mid-2026 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 rather than as a genuine slowdown.
Two views of the same 1,039 records: how filing volume has moved year over year, and which IPC subclasses carry the claim density.
Filings rose to a peak of 113 records in 2018, then eased. On the last complete three-year comparison, 2021 (43) fell to 2024 (28), a -35% move; 2025 and 2026 figures are still filling in under publication lag and should not be read as a continued decline yet.
C12N (microorganisms and genetic engineering) touches 98.3% of records, confirming the corpus is fundamentally about the cell line and its engineered biology. C12P (fermentation) at 51.9% and C07K (peptides/proteins) at 48.7% show the second layer is production biochemistry, while C12M (bioreactor apparatus) at 14.2% and C12Q (enzyme/DNA testing) at 2.3% mark where the physical and analytical tooling around harvest decisions is comparatively under-claimed.
Shares are the percentage of the 1,039 records in scope. A patent can carry several IPC classes, so the shares add up to more than 100%.
This page is one run against one query. Ask Eureka your own question about mammalian cell culture harvest timing and every answer comes back with the patent numbers behind it.
Try EurekaThe present disclosure pertains to a mammalian cell culture genetically modified to express, and which expresses, a neublastin antibody polypeptide, or fragment thereof, in the culture, and to a neublastin antibody polypeptide, or fragment thereof, made by a mammalian cell culture genetically modified to express, and which expresses, the neublastin antibody polypeptide, or fragment thereof.Filed as US20190194602A1, this record illustrates how a therapeutic-molecule claim is anchored to a specific genetically modified culture rather than to a harvest-timing method as such — a pattern worth checking against before drafting new process claims.


| # | Publication no. | Patent title | Citations |
|---|---|---|---|
| 1 | US5510262A | Cell-culturing apparatus and method employing a macroporous support | 165 |
| 2 | WO2013006479A2 | Mammalian cell culture | 156 |
| 3 | WO2006026445A1 | Production of polypeptides | 133 |
| 4 | US20090042253A1 | Use of perfusion to enhance production of fed-batch cell culture in bioreactors | 121 |
| 5 | WO2011134920A1 | Improved cell culture medium | 107 |
| 6 | US5232848A | Basal nutrient medium for cell culture | 100 |
| 7 | WO2004058800A2 | Mammalian cell culture processes for protein production | 99 |
| 8 | WO2011134919A2 | Improved cell cultivation process | 84 |
| 9 | US20050019859A1 | Mammalian ceII culture processes for protein production | 81 |
| 10 | WO2007076032A2 | Compositions and methods for producing a composition | 80 |
Citation counts reward older filings that have had more time to accumulate references — treat this as a map of influence within the searched corpus, not a ranking of current commercial importance.
Each row carries its publication number; clicking a row searches Eureka by that number.
When you want the answer in the next five minutes.
The agent works the prompt against patents and technical literature, citing every source.
Run your analysis now →When it has to run inside your own pipeline.
Patent search, landscape analysis and assignee resolution as MCP tools. Drop them into any agent framework, or call REST directly.
Browse MCP servers →Three read-throughs from the concentration, trend and classification figures above.
With the five largest filers already holding 55.2% of all 1,039 records and the leading ten at 75.2%, a new entrant competing on filing volume in core cell-engineering claims is competing against incumbents with deep, overlapping portfolios. Differentiation is more realistic in adjacent process or analytical claims than in the crowded core.
Filing peaked at 113 records in 2018 and has since settled to a lower plateau, with the last comparable complete years showing a -35% move from 2021 to 2024. Because publication lag understates 2025-2026, this should be read as cooling from an unusually active period rather than as the field going quiet.
C12N claims touch 98.3% of records and C12P/C07K each cover roughly half, but C12M (bioreactor apparatus) sits at only 14.2% and C12Q (enzyme/DNA testing methods) at 2.3%. The instrumentation and assay layer that actually triggers a harvest decision is far less crowded than the cell-line and production biochemistry layers around it.
Eureka can read the same corpus for gaps instead of for coverage: under-claimed branches adjacent to mammalian cell culture harvest timing, with the prior art for and against each one.
The ranked leaders account for three-quarters of the field between the top ten alone; co-assignment activity is limited, and recent-year momentum has cooled across the largest filers even before publication lag is accounted for.
The top-ranked assignee's 317 records dwarf the fifth-place figure of 53 and the tenth-place figure of 34, meaning the drop-off after the leader is sharp rather than gradual.
Combined, the leading ten assignees account for 781 of the 1,039 records in scope, or 75.2%. That leaves a long tail of single- or few-filing entrants competing for the remaining quarter.
Only ten co-assignee pairs appear across the dataset, with the strongest pairing recorded at 19 shared records. Most large filers are prosecuting independently rather than jointly, which limits how much freedom-to-operate risk is shared across organisational lines.
Several of the largest assignees show 0 records in the latest year, with year-on-year drops as steep as -100%, and one shows -80% YoY. Given publication lag, this is partly an artefact of the reporting window rather than proof these organisations have stopped filing.
| Assignee | Recent year | YoY |
|---|---|---|
| Regeneron Pharmaceuticals, Inc. | 1 | -80% |
| Amgen Inc. | 0 | -100% |
| Genentech, Inc. | 0 | -100% |
| Biogen MA Inc. | 0 | — |
| F. Hoffmann-La Roche AG | 0 | — |
| Boehringer Ingelheim International GmbH | 0 | -100% |
| UCB Biopharma SPRL | 0 | — |
| Novartis AG | 0 | — |
The landscape points to where claim space is open and where it is not; the next step is testing a specific claim idea against the full record set.
With three-quarters of records held by ten organisations, a new filing in core cell-engineering or fermentation claims needs a clearance check against those specific portfolios before drafting begins.
Run a freedom-to-operate check in EurekaC12M and C12Q coverage is thin relative to the cell-biology core, suggesting more room for hardware-integrated or in-line assay claims tied to harvest decisions.
Explore white space in EurekaRecent-year momentum has dropped across several top assignees, but publication lag means the real picture is still forming — worth monitoring as 2025-2026 data fills in.
Set up assignee tracking in EurekaThe dataset shows a clear leader with 317 records, well ahead of the fifth-place assignee at 53 and the tenth at 34. The leading ten organisations together account for 781 of the 1,039 records in scope, or 75.2%, so filing activity is heavily concentrated rather than evenly spread across the field. A new entrant should expect to be filing into a space where a handful of large biologics companies already hold dense, overlapping claim positions.
Filing peaked at 113 records in 2018 and has eased since, with the most recent complete comparison showing a -35% move from 43 records in 2021 to 28 in 2024. Because patent publication typically lags filing by around 18 months, the 2025 and 2026 figures in any dataset are still incomplete and should not be read as proof the field has gone quiet. The safer read is that activity has cooled from an unusually active 2017-2018 period rather than that interest has disappeared.
Classification data shows C12N (microorganisms and genetic engineering) touching 98.3% of records, while C12M (bioreactor apparatus) sits at 14.2% and C12Q (enzyme and DNA testing methods) at just 2.3%. That gap suggests the instrumentation and in-line assay layer that actually triggers a harvest decision — sensors, real-time viability modelling, integrated titer monitoring — is comparatively open relative to the crowded cell-engineering core. Filers looking for less contested claim space should look at that hardware and assay layer rather than the biology itself.
US20190194602A1 claims a genetically modified mammalian cell culture that expresses a neublastin antibody polypeptide, along with the antibody product made by that culture. It anchors its claims to a specific engineered cell line and molecule rather than to a general harvest-timing method, so it primarily blocks close variants of that particular antibody-producing culture rather than harvest-decision logic broadly. Anyone drafting a process claim around viability or titer signals should still check it, but it is not a blanket barrier to harvest-timing method claims generally.
Co-assignment is uncommon in this landscape: only ten co-assignee pairs appear across the full dataset, and the strongest pairing covers 19 shared records. Most of the largest filers prosecute independently, which means portfolio risk and claim overlap are concentrated within single organisations rather than spread across joint ventures. This matters for freedom-to-operate analysis because it narrows the number of parties a new filer needs to clear against for any given large portfolio.
Go past this page: query the whole mammalian cell culture harvest timing corpus yourself, in your own scope.
Every answer comes back with patent numbers you can open.
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.