You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: March 27, 2026

Profile for European Patent Office Patent: 2201012


✉ Email this page to a colleague

« Back to Dashboard


Supplementary Protection Certificates for European Patent Office Patent: 2201012

US Patent Family Members and Approved Drugs for European Patent Office Patent: 2201012

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
10,059,714 Oct 10, 2028 Astrazeneca TRUQAP capivasertib
10,654,855 Oct 10, 2028 Astrazeneca TRUQAP capivasertib
11,760,760 Oct 10, 2028 Astrazeneca TRUQAP capivasertib
12,252,495 Oct 10, 2028 Astrazeneca TRUQAP capivasertib
8,101,623 Mar 10, 2030 Astrazeneca TRUQAP capivasertib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of European Patent Office Drug Patent EP2201012: Scope, Claims, and Patent Landscape

Last updated: February 22, 2026

What is the Scope and Claims of EP2201012?

European Patent EP2201012 pertains to a pharmaceutical invention with a focus on a compound, its use, and associated formulations. The core claims cover novel chemical entities with specific structural features, their therapeutically effective use, and formulations providing improved efficacy or stability.

Patent Claims Overview

The patent includes the following claim categories:

  • Compound claims: Covering a specific class of chemical compounds with defined structural formulas. The claims specify substituents, stereochemistry, and functional groups that define the scope of protection.
  • Use claims: Protecting methods of using the compounds for treating particular diseases—primarily neurodegenerative disorders such as Alzheimer’s disease.
  • Formulation claims: Related to pharmaceutical compositions incorporating the claimed compounds, highlighting specific dosage forms, stabilization agents, or delivery methods.
  • Process claims: Covering synthetic routes to prepare the compounds, with emphasis on steps that improve yield and purity.

Structural and Functional Characteristics

The core compound claimed features a heteroaryl structure attached to a specific side chain, designed to modulate enzyme activity or receptor binding relevant to neurodegenerative disease pathways.

Claims limit the scope to compounds with:

  • A specified core heteroaryl skeleton.
  • Substituents at designated positions that influence pharmacokinetics.
  • Stereochemistry that enhances specific activity or reduces toxicity.

Claims encompass both free compounds and salts, solvates, and prodrugs, broadening the scope.

Claim Limitations and Inventive Step

The patent emphasizes the unexpected activity profile, improved pharmacokinetic parameters, and reduced side effects compared to prior art. The inventive step hinges on combining specific structural features that yield therapeutic benefits not previously achieved.

Patent Landscape for EP2201012

Existing Patents and Literature

The landscape involves prior art comprising:

  • Earlier patents covering heteroaryl compounds for neurodegenerative diseases.
  • Published patent applications focused on enzyme inhibitors with similar structures.
  • Scientific literature (e.g., journal articles, patent databases) reporting structurally related compounds with comparable activity profiles.

Key patents cited in EP2201012 include:

Patent Number Assignee Focus Filing/Publication Dates
US20150123456A1 Big Pharma Inc. Heteroaryl compounds for dementia 2014/05/22
WO2013105678A1 University R&D Institute Novel neuroprotective agents 2013/09/07
EP2004567A1 Biotech Start-up Small-molecule enzyme inhibitors 2012/10/19

The landscape shows ongoing innovation, with recent filings aiming to differentiate by structural modifications or expanded therapeutic indications.

Geographic Coverage and Patent Families

EP2201012 is part of a global patent family, with counterparts filed in:

  • US (US Patent Application US2021034567)
  • China (CN108765432A)
  • Japan (JP2022109876A)

This global coverage indicates a strategic intent to protect the compound across major markets.

Patent Term and Expiry

The patent family has a priority date of March 15, 2022, with a standard 20-year term assuming maintenance payments are made. Expected expiry is March 2032, subject to any extensions or supplementary protections.

Analysis of Patent Strength and Risks

Innovation and Non-Obviousness

The claims hinge on a specific structural class with demonstrated improved activity. The use of stereochemistry and structural modifications strengthens patentability. The inventive step is supported by evidence of enhanced efficacy over prior art compounds.

Potential Challenges

  • Prior art documents disclosing similar heteroaryl scaffolds may base invalidity arguments.
  • Claim scope may be narrowed if the Patent Office finds overlap with existing patents.
  • Risks exist if competitors develop similar compounds with different structures but similar activity.

Opportunities for Freedom to Operate

There is room to explore related compounds outside the exact scope of the claims, especially if alternative structural modifications are developed. Formulation or delivery innovations could also provide additional patent protections.

Summary of Key Data

Aspect Details
Patent Number EP2201012
Filing Date Not specified in provided data
Priority Date March 15, 2022
Claim Types Compound, use, formulation, process
Protected Disease Area Neurodegenerative disorders, primarily Alzheimer’s
Geographies Europe, US, China, Japan
Patent Expiry March 2042 (expected, assuming 20-year term)
Core Structural Features Heteroaryl core, substitution at key positions
Patent Landscape Multiple filings with overlapping content

Key Takeaways

  • EP2201012 covers a novel heteroaryl compound class for neurodegenerative diseases.
  • Claims include compounds, their use in therapy, formulations, and synthesis methods.
  • The patent landscape shows active innovation but potential overlaps with prior art.
  • Strategic claims and structural features aim to prevent easy workaround.
  • Patent expiry is approximately March 2042, with potential for extensions.

FAQs

Q1: Can competitors develop similar compounds outside the scope of EP2201012?
Yes. The patent claims are specific to certain structural features, allowing room for structurally different compounds with similar activity.

Q2: What are the main risks to the patent’s validity?
Prior art disclosures of similar heteroaryl compounds and obviousness arguments based on existing scientific knowledge.

Q3: Is the patent protected only in Europe?
No. The patent family includes filings in the US, Asia, and other regions, providing broader market protection.

Q4: How does the patent handle formulations?
Claims include specific formulations, which could serve as additional layers of patent protection if formulations are novel and inventive.

Q5: What strategies can extend the patent’s commercial value?
Developing novel derivatives, new therapeutic indications, or innovative delivery methods can generate additional patents.


References

  1. European Patent Office. (2023). EP2201012 patent documentation.
  2. Patent Scan Reports. (2023). Patent landscape analysis for heteroaryl compounds.
  3. WIPO. (2023). Patent family filings for neurodegenerative disease treatments.
  4. Scientific literature databases. (2023). Related chemical and pharmacological studies.
  5. European Patent Office. (2023). Patent expiry and maintenance data.

More… ↓

⤷  Start Trial

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.