Abstract: Provided are methods of treating malaria comprising administration of compounds of Formula (I), or a pharmaceutically acceptable salt thereof, to a subject in need thereof, wherein the variables are as defined herein. Also provided are uses of the compounds of Formula (I), as defined herein, for inhibiting plasmepsin X, plasmepsin IX or plasmepsin X and IX activity, for treating a Plasmodium infection, and for treating malaria. Also provided are methods of treatment further comprising administration of one or more additional anti-malarial compounds.
Type:
Application
Filed:
December 5, 2022
Publication date:
February 27, 2025
Applicants:
Merck Sharp & Dohme LLC, The Walter and Eliza Hall Institute of Medical Research, MSD R&D (China) Co., Ltd.
Inventors:
John A. McCauley, Manuel De Lera Ruiz, Zhuyan Guo, Philippe Nantermet, Michael J. Kelly, III, Alvaro Gutierrez Bonet, Lianyun Zhao, Zhiyu Lei, Bin Hu, Dongmei Zhan, Anthony Hodder
Abstract: The disclosure relates to stable RSV F proteins and immunogenic compositions containing the same, as well as methods of using the immunogenic compositions and compositions comprising the RSV F proteins.
Type:
Grant
Filed:
December 20, 2022
Date of Patent:
February 25, 2025
Assignee:
Merck Sharp & Dohme LLC
Inventors:
Lan Zhang, Arthur Fridman, Eberhard Durr, Andrew Bett
Abstract: Provided are novel Substituted Thiophene Derivatives of Formula (I) and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, and R7 are as defined herein, as well as compositions comprising at least one Substituted Thiophene Derivative, and methods of using the Substituted Thiophene Derivatives for treating or preventing cancer in a patient.
Type:
Application
Filed:
December 15, 2022
Publication date:
February 20, 2025
Applicant:
Merck Sharp & Dohme LLC
Inventors:
David A. Candito, Matthew L. Childers, Duane E. DeMong, Christian Fischer, Xavier Fradera, James P. Jewell, Shuhei Kawamura, Ping Liu, Charles S. Yeung, Xiao Mei Zheng, Kaitlyn Marie Logan, Ryan D. Otte, Chunhui Huang, Sebastian E. Schneider
Abstract: A liquid-crystal (LC) medium containing one or more dyes and one or more polymerizable compounds, its use for optical, electro-optical and electronic purposes, in particular in LC displays, especially in colour LC displays of the PSA (polymer sustained alignment) or SA (self-aligning) mode containing a quantum dot colour filter (QDCF), an LC display of the PSA or SA mode containing the LC medium and containing a QDCF, and to a process of manufacturing the LC display.
Abstract: The present invention relates to combination therapies useful for the treatment of cancer. In particular, the invention relates to a therapeutic combination which comprises a PD-1 antagonist, an ATR inhibitor and a platinating agent.
Type:
Grant
Filed:
September 26, 2019
Date of Patent:
February 18, 2025
Assignee:
Merck Patent GMBH
Inventors:
Marat Alimzhanov, Patricia Soulard, Frank Zenke, Heike Dahmen, Astrid Zimmermann, Andreas Schroeder, Keyvan Tadjalli Mehr, Martin Falk
Abstract: The present disclosure provides novel anhydrate crystalline Forms 1 and 4 of 4?-Ethynyl-2-fluoro-2?-deoxyadenosine and pharmaceutical compositions thereof, each of which may be useful for the inhibition of HIV reverse transcriptase, the treatment or prophylaxis of HIV infection and/or the treatment, prophylaxis and/or delay in the onset or progression of AIDS or ARC.
Type:
Grant
Filed:
December 16, 2019
Date of Patent:
February 18, 2025
Assignee:
Merck Sharp & Dohme LLC
Inventors:
Daniel Skomski, Yongchao Su, Wei Xu, Marko Cubrovic, Stephanie Elizabeth Barrett
Abstract: Monovalent IL-12 heterodimeric Fc proteins that display attenuated potency at the IL-12 receptor compared to wild-type IL-12 and have an extended half-life compared to wild-type IL-12 are described. The monovalent heterodimeric IL-12 heterodimeric Fc proteins comprise a heterodimer comprising an IL-12p35 subunit first Fc domain fusion protein and an IL-p40 subunit second Fc domain fusion protein IL-12 and Fc domains wherein the first and second Fc domains comprise modifications that facilitate heterodimerization of the first Fc domain to the second Fc domain.
Type:
Application
Filed:
August 8, 2024
Publication date:
February 13, 2025
Applicant:
MERCK SHARP & DOHME LLC
Inventors:
Mehabaw Getahun Derebe, Ghassan N. Fayad, Veronica M. Juan, Mike Lee, Ji Hea Park, Piyali Saha, Fan Zhang
Abstract: The present invention relates to novel 5-azaindazole derivatives of formula (I), as described and defined herein, and pharmaceutically acceptable salts, solvates and prodrug thereof, as well as pharmaceutical compositions comprising such compounds. The 5-azaindazole derivatives according to the invention have been found to be highly effective dual A2A/A2B adenosine receptor antagonists, and can thus be used as therapeutic agents, particularly in the treatment or prevention of hyperproliferative or infectious diseases or disorders.
Type:
Application
Filed:
October 24, 2024
Publication date:
February 13, 2025
Applicant:
MERCK PATENT GMBH
Inventors:
Anne-Laure BLAYO, Baptiste MANTEAU, Camille AMALRIC, Stanislas MAYER, Stephan SCHANN, Mickaƫl FER
Abstract: Provided are novel Pyrazolopyrimidine Derivatives of Formula (I): and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, and R4 are as defined herein. Also provided are compositions comprising at least one Pyrazolopyrimidine Derivative, and methods of using the Pyrazolopyrimidine Derivatives for treating or preventing a herpesvirus infection in a patient.
Type:
Application
Filed:
December 13, 2022
Publication date:
February 13, 2025
Applicant:
Merck Sharp & Dohme LLC
Inventors:
Kira A. Armacost, Andrew J. Cooke, Christopher Douglas Cox, Brendan M. Crowley, Marc A. Labroli, Michael A. Plotkin, Izzat T. Raheem, Kelly-Ann S. Schlegel, Anthony W. Shaw, David M. Tellers
Abstract: A silicon precursor compound according to Formula I as described herein is used to form a silicon-containing thin film having excellent quality. A preparation method therefor, and a silicon-containing thin film preparation method using the silicon precursor compound are also described.
Abstract: The present disclosure provides methods for the acute treatment of migraine with or without aura, comprising the administration of ubrogepant. In particular, the present disclosure provides methods for the acute treatment of migraine in patients having hepatic impairment; in patients with renal impairment; and in patients concurrently taking CYP3A4 modulators or BCRP and/or P-gp only inhibitors.
Type:
Grant
Filed:
July 18, 2024
Date of Patent:
February 11, 2025
Assignee:
Merck Sharp & Dohme LLC
Inventors:
Mary Ann Johnson, Leonardo R. Allain, W. Mark Eickhoff, Craig B. Ikeda, Chad D. Brown, Francis J. Flanagan, Jr., Rebecca Nofsinger, Melanie J. Marota, Lisa Lupton, Paresh B. Patel, Hanmi Xi, Wei Xu
Abstract: A semiconducting light emitting nanoparticle is described having a core and shell structure. The particle has a core and an outer layer or shell. The outer layer covers at least part of the core and contains a metal cation and a divalent anion. Additionally, one or more organic moieties are directly attached to the anion of the outer layer by covalent bond. The divalent anion is Se2?, S2?, Te2?, O2? or a combination thereof. The metal cation can be a monovalent, cation, trivalent, or tetravalent cation. Also, a process for synthesizing the semiconducting light emitting nanoparticle is described.
Type:
Grant
Filed:
April 23, 2020
Date of Patent:
February 11, 2025
Assignee:
MERCK PATENT GMBH
Inventors:
Elizaveta Kossoy, Shany Neyshtadt, Sanaa Khalil, Alex Rabkin, Jessica Benjamini Ettedgui
Abstract: The present invention refers to a crystalline salt comprising 5-methyl-(6S)-tetrahydrofolic acid and an amino acid ethyl ester like L-phenylalanine ethyl ester or L-methionine ethyl ester, wherein the molar ratio of 5-methyl-(6S)-tetrahydrofolic acid to amino acid ethyl ester is from 1:0.3 to 1:3.0 (in mol/mol) and/or hydrates and/or solvates thereof as well as to a process of obtaining the same.
Type:
Grant
Filed:
July 2, 2019
Date of Patent:
February 11, 2025
Assignee:
MERCK PATENT GMBH
Inventors:
Rudolf Moser, Viola Groehn, Ruth Boehni Stamm, Fritz Blatter, Martin Szelagiewicz
Abstract: The present invention provides a number of process improvements related to the conjugation of capsular polysaccharides from Streptococcus pneumoniae to a carrier protein. These processes are serotype specific and include acid hydrolysis, addition of sodium chloride to the reductive amination reaction, and addition of sucrose to dissolve polysaccharides. Polysaccharide-protein conjugates prepared using the processes of the invention can be included in multivalent pneumococcal conjugate vaccines.
Abstract: Method and system to analyze biomasses in a bioreactor (3) via a computer (2) with a system software (5), the bioreactor (3) having at least one sensor (6) to measure the biomasses and which has a data connection to the computer (2) managed by a data interface provided by the system software (5), wherein the system software (5) provides a data conversion model (8) to analyze real time raw data about permittivity measured by and transmitted from the at least one sensor (6) to the computer (2) to calculate specific cell parameters of cells in the biomasses.
Abstract: Disclosed herein are biomarkers that correlate with responses to an anti-ILT4 and anti-PD-1 combination therapy. A biomarker that can differentiate responders from non-responders to this combination therapy can potentially be used to select human subjects who have a higher probability to benefit from such a combination therapy. In one embodiment, a combined positive score (CPS) for PD-L 1 expression in a tumor sample from a human subject is used as a biomarker to differentiate a responder from a non-responder to an anti-ILT4 and anti-PD-1 combination therapy. In another embodiment, a T-cell-inflamed gene expression profile (TcellinfGEP) score is used as a biomarker to differentiate a responder from a non-responder to an anti-ILT4 and anti-PD-1 combination therapy.
Type:
Application
Filed:
December 15, 2022
Publication date:
February 6, 2025
Applicant:
Merck Sharp & Dohme LLC
Inventors:
Rachel Allison Altura, Jared Lunceford, Julia F. Markensohn, Leah Suttner, Douglas C. Wilson
Abstract: The new media exhibit a ferroelectric nematic phase preferably at ambient temperature. They preferably comprise one or more compounds selected from the group of compounds of formulae IA, IB and IC, in which the variable groups have the meanings indicated in the text and in the claims. Use of the media for providing ferroelectric nematic materials and a method of operation of an electro-optical device are presented. The media may be useful for energy-saving displays and electrical appliances.
Type:
Grant
Filed:
November 30, 2021
Date of Patent:
February 4, 2025
Assignee:
MERCK PATENT GMBH
Inventors:
Matthias Bremer, Atsutaka Manabe, Martin Kraska