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The agent works the prompt against patents and technical literature, citing every source.
Run your analysis now →Filing growth compares 2021 (153 records) with 2024 (129) — 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 3,016 records in scope (CR5), not by the ranked leaders only.
Degraders solve a target-engagement problem but inherit a pharmacokinetics problem: high molecular weight, poor membrane permeability and efflux liability routinely cap oral exposure long before potency becomes the limiting factor. This landscape tracks the patent activity built around that constraint — filings that address molecular weight penalty, metabolic stability, formulation enabling and tissue distribution alongside degrader-specific chemistry, rather than degrader mechanism of action alone.
The scope spans 3,016 published records filed between 2015 and 2026, drawn from applicants ranging from large pharmaceutical originators to university technology-transfer offices and single-asset biotechs. Because publication lags filing by roughly 18 months, the 2025 and 2026 counts in the trend are still filling in and understate real filing activity in those years.
Two views of the same 3,016-record corpus: how filing volume has moved year over year, and which IPC subclasses carry the claim density.
Filings peaked in 2018 at 214 and have since settled into a lower, more stable band; the 2021-to-2024 comparison (153 to 129, a 16% decline) is the most reliable recent read, since later years are still being published.
A61K (medicinal preparations, 79.9% of records) and C07D (heterocyclic compounds, 61.2%) anchor the field; C07F organo-metallic chemistry (10.1%) and C07K peptides (5.7%) are present but comparatively thin, and A01N biocide-adjacent filings (3.8%) sit at the field's edge.
Shares are the percentage of the 3,016 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 degrader pharmacokinetics and modality limits and every answer comes back with the patent numbers behind it.
Try EurekaThe disclosure relates, inter alia, to a library of transcriptional data, and methods for assembling and using same.Filed 2025-03-13, this record sits at the data-infrastructure edge of the field rather than in composition-of-matter claims — a marker of how PK optimisation work is increasingly supported by computational and data-library filings alongside chemistry claims.


| # | Publication no. | Patent title | Citations |
|---|---|---|---|
| 1 | WO2012034091A1 | Imidazo [1, 2] pyridazin compounds and compositions as TRK inhibitors | 183 |
| 2 | US20050209246A1 | Prodrugs of piperazine and substituted piperidine antiviral agents | 183 |
| 3 | WO2012084711A1 | N-substituted azetidine derivatives | 168 |
| 4 | WO2019167000A1 | Pharmaceutical compounds | 155 |
| 5 | WO2012006475A1 | Compounds and methods for inhibiting phosphate transport | 142 |
| 6 | US7745625B2 | Prodrugs of piperazine and substituted piperidine antiviral agents | 140 |
| 7 | WO2007059312A2 | Methods and compositions comprising non-natural amino acids | 125 |
| 8 | US8637516B2 | Compounds and compositions as TRK inhibitors | 122 |
| 9 | WO2013025805A1 | Substituted (e)-n'-(1-phenylethylidene) benzohydrazide analogs as histone demethylase inhiitors | 120 |
| 10 | WO2009091388A2 | Triazines and related compounds having antiviral activity, compositions and methods thereof | 119 |
Citation counts favour older filings simply because they have had longer to accumulate citations inside this searched corpus — treat them as evidence of influence on subsequent claim drafting, not as a ranking of current technical 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 readings of the same dataset, aimed at where to file, who to watch, and where claim space is still open.
981 of the 3,016 records in scope belong to the five most active assignees, with the leader alone holding 299. That is real concentration in composition-of-matter and formulation claims touching PK limitation, but it still leaves two-thirds of the corpus distributed across the remaining ranked assignees and unranked single-filers.
Filings dropped from 153 in 2021 to 129 in 2024, a 16% pullback over the only three-year span in this dataset that is fully comparable. That is consistent with a field consolidating around known chemotypes rather than one being abandoned — several of the largest historical filers show sharply reduced or zero filings in the latest year, which reads as portfolio maturity as much as retreat.
A61K and C07D carry the bulk of claim density, at 79.9% and 61.2% of records respectively. C07F organo-metallic chemistry (10.1%) and C07K peptide and protein claims (5.7%) are present but far less crowded, which is where structurally distinct PK-mitigation approaches are more likely to clear prior art.
Eureka can read the same corpus for gaps instead of for coverage: under-claimed branches adjacent to degrader pharmacokinetics and modality limits, with the prior art for and against each one.
The ranked assignee list returns 100 companies scored by family count; a handful of academic, mid-cap and large-pharma filers account for the concentration at the top, while momentum in the latest year has slowed sharply even among the leaders.
The leading assignee holds 299 of the 3,016 records in scope, roughly a third larger than the fifth-place holder at 121. That gap suggests a genuinely dominant position in this specific claim space rather than a crowded top tier.
By tenth place, family counts have fallen to 65 — well under a quarter of the leader's total. Combined, the top ten hold 1,338 records, 44.4% of all records in scope, which means more than half the corpus is spread thin across the remaining ranked and unranked filers.
More than one of the most historically active assignees in this corpus, including academic and mid-cap filers, show zero filings in the latest tracked year, and one large filer with a strong recent run is down 59% year over year. That does not necessarily mean exit — it is consistent with the 18-month publication lag masking work still in the pipeline.
| Assignee | Recent year | YoY |
|---|---|---|
| Kumquat Biosciences Inc | 7 | -59% |
| Ardelyx Inc | 0 | -100% |
| Astex Therapeutics Ltd | 0 | — |
| University of Tennessee Research Foundation | 0 | — |
| Cancer Research Technology Ltd | 0 | — |
| Bayer Pharma AG | 0 | — |
| AstraZeneca AB | 0 | — |
| Otsuka Pharmaceutical Co., Ltd. | 0 | -100% |
The dataset points to specific next steps depending on whether the goal is freedom-to-operate, portfolio strategy or scouting.
Organo-metallic and peptide-based routes carry a fraction of the claim density seen in A61K and C07D. A targeted search inside those subclasses can surface whether a specific structural approach is genuinely open or simply under-indexed.
Explore in EurekaSeveral top-ten filers show zero or sharply reduced activity in the latest year. Watching for renewed filing, licensing moves or continuation activity from those assignees is a cheap way to catch a re-entry early.
Set up monitoring in EurekaWith 3,016 published records collapsing to 3,016 tracked families in this corpus, family-level analysis avoids overweighting continuation-heavy applicants when scoping a clearance search.
Run a family-level search in EurekaDegraders, particularly bifunctional molecules, routinely exceed classical rule-of-five limits on molecular weight and polar surface area, which caps oral bioavailability regardless of how potent the binding is. That has pushed a large share of recent claim activity toward molecular weight penalty, metabolic stability and formulation-enabling technology rather than target engagement alone. In this dataset, 79.9% of the 3,016 records in scope touch A61K medicinal-preparation claims, which is where much of this formulation and exposure work is captured.
The ranked assignee list returns 100 companies, with the leader holding 299 of the 3,016 records in scope and a fifth-place holder at 121. The top five assignees combined account for 981 records, or 32.5% of all records, showing real concentration at the top even though the ranking itself covers a broad set of academic, mid-cap and large-pharma filers. Individual identities and their exact standings are best read directly from the ranking table rather than summarised here, since positions shift as new records publish.
Filings fell from 153 in 2021 to 129 in 2024, a 16% decline over the most recent three-year span that can be treated as complete. That is a real pullback but not a collapse, and it should not be read from 2025 or 2026 figures, since publication typically lags filing by about 18 months and those years are still filling in. The more informative signal is that several previously dominant assignees show zero filings in the latest tracked year, which is consistent with portfolio consolidation around established chemotypes.
The composition data shows A61K and C07D carrying the bulk of claim density, at 79.9% and 61.2% of the 3,016 records respectively, while C07F organo-metallic chemistry sits at 10.1% and C07K peptide-based claims at just 5.7%. Those lower-density subclasses are where structurally distinct approaches to PK mitigation, such as organo-metallic warhead linkers or peptide-based scaffolds, are less likely to run into dense prior art. A first claim there would need to tie the structural novelty directly to a specific PK outcome, such as reduced efflux liability, to differentiate from the dominant small-molecule chemotypes.
Citation counts in this corpus favour older filings simply because they have had more time to accumulate citations, so the most-cited records skew toward filings from the earlier part of the 2015-2026 window. They are a reasonable signal of which claims shaped later drafting in the field, but a poor proxy for which technology is most commercially relevant today. For current relevance, filing recency, assignee momentum and IPC composition are more useful than citation rank alone.
Go past this page: query the whole degrader pharmacokinetics and modality limits 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.
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