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Routine Rule Added Final

Patent Application: Fused Azole Derivatives as Diacylglyceride Inhibitors

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Published March 11th, 2026
Detected March 26th, 2026
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Summary

The European Patent Office has published patent application EP4626881A1 for fused azole derivatives developed by Merck Sharp & Dohme LLC. These compounds are identified as novel diacylglyceride O-acyltransferase 2 inhibitors, potentially impacting treatments for metabolic and cardiovascular diseases.

What changed

The European Patent Office (EPO) has published a new patent application, EP4626881A1, detailing fused azole derivatives designed as diacylglyceride O-acyltransferase 2 (DGAT2) inhibitors. The applicant, Merck Sharp & Dohme LLC, claims these compounds are novel and may be useful in treating conditions related to DGAT2 activity, such as obesity, diabetes, and cardiovascular diseases. The application includes specific chemical structures and classifications (IPC: C07D) and lists designated states across Europe where patent protection is sought.

This publication represents the grant of a patent application, not a regulatory rule imposing obligations. However, it signifies the EPO's recognition of potential intellectual property in this area of pharmaceutical research. Companies involved in drug development, particularly those targeting metabolic pathways or cardiovascular health, should be aware of this patent as it may affect their own research and development activities or potential licensing opportunities. No immediate compliance actions are required for entities outside of Merck Sharp & Dohme LLC, but it highlights a specific area of innovation in pharmaceutical chemistry.

Source document (simplified)

← EPO Patent Bulletin

PREPARATION OF FUSED AZOLE DERIVATIVES AS NOVEL DIACYLGLYCERIDE O-ACYLTRANSFERASE 2 INHIBITORS

Publication EP4626881A1 Kind: A1 Mar 11, 2026

Applicants

Merck Sharp & Dohme LLC

Inventors

LIM, Yeon-Hee, HUGELSHOFER, Cedric L., ROANE, James P., SHOCKLEY, Samantha E.

IPC Classifications

C07D 409/14 20060101AFI20240607BHEP C07D 413/12 20060101ALI20240607BHEP C07D 413/14 20060101ALI20240607BHEP C07D 417/14 20060101ALI20240607BHEP C07D 471/04 20060101ALI20240607BHEP C07D 487/04 20060101ALI20240607BHEP C07D 498/04 20060101ALI20240607BHEP C07D 513/04 20060101ALI20240607BHEP A61P 3/00 20060101ALI20240607BHEP A61P 9/00 20060101ALI20240607BHEP A61P 25/00 20060101ALI20240607BHEP

Designated States

AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LI, LT, LU, LV, MC, ME, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR

View original document →

Classification

Agency
EPO
Published
March 11th, 2026
Instrument
Rule
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
EP4626881A1

Who this affects

Applies to
Drug manufacturers Pharmaceutical companies
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Drug Development Patent Filing
Geographic scope
European Union EU

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Legal
Compliance frameworks
FDA 21 CFR Part 11
Topics
Drug Development Intellectual Property

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