USPTO Grants PRMT5 Inhibitors Patent to Merck Sharp & Dohme
Summary
The USPTO has granted a new patent (US12583871B2) to Merck Sharp & Dohme LLC for PRMT5 inhibitors. The patent covers compounds and methods for treating conditions such as cancer, sickle cell, and hereditary persistence of foetal hemoglobin.
What changed
The United States Patent and Trademark Office (USPTO) has granted patent US12583871B2 to Merck Sharp & Dohme LLC. This patent covers novel compounds identified as PRMT5 inhibitors, along with their pharmaceutically acceptable salts, esters, and prodrugs. The invention also includes methods for synthesizing these compounds, pharmaceutical compositions containing them, and their therapeutic applications for treating cancer, sickle cell disease, and hereditary persistence of foetal hemoglobin (HPFH) mutations.
This patent grant signifies a new intellectual property asset for Merck Sharp & Dohme in the area of oncology and genetic disorders. While this is a patent grant and not a regulatory rule imposing direct compliance obligations on other entities, it highlights a specific area of innovation and potential future drug development. Companies operating in the pharmaceutical sector, particularly those involved in developing treatments for cancer or blood disorders, should be aware of this granted patent as it may impact their own research and development strategies or potential licensing opportunities.
Source document (simplified)
PRMT5 inhibitors
Grant US12583871B2 Kind: B2 Mar 24, 2026
Assignee
Merck Sharp & Dohme LLC
Inventors
Michelle Machacek, Michael D. Altman, Shuhei Kawamura, David L Sloman, David J. Witter, Craig R. Gibeau
Abstract
The present invention provides a compound selected from: and the pharmaceutically acceptable salts, esters, and prodrugs thereof, which are PRMT5 inhibitors. Also provided are methods of making compounds disclosed herein, pharmaceutical compositions comprising compounds disclosed herein, and methods of using these compounds to treat cancer, sickle cell, and hereditary persistence of foetal hemoglobin (HPFH) mutations.
CPC Classifications
C07D 519/00
Filing Date
2020-12-14
Application No.
17787135
Claims
16
Named provisions
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