Remimazolam: Non-Clinical and Clinical Profile of a New Sedative/Anesthetic Agent

被引:164
作者
Kilpatrick, Gavin J. [1 ]
机构
[1] GJK Pharma Ltd, Eltisley, England
关键词
remimazolam; sedation; anesthesia; benzodiazepine; midazolam; propofol; total intravenous anesthesia; short-acting anesthetic; CNS; 7056; GENERAL-ANESTHETICS; HUMAN CARBOXYLESTERASES; PROCEDURAL SEDATION; DRUG DEVELOPMENT; MIDAZOLAM; EFFICACY; SAFETY; BENZODIAZEPINES; PROPOFOL;
D O I
10.3389/fphar.2021.690875
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A program to identify novel intravenous sedatives with a short and predictable duration of action was initiated in the late 1990's by Glaxo Wellcome. The program focussed on the identification of ester-based benzodiazepine derivatives that are rapidly broken down by esterases. Remimazolam was identified as one of the lead compounds. The project at Glaxo was shelved for strategic reasons at the late lead optimization stage. Via the GSK ventures initiative, the program was acquired by the small biotechnology company, TheraSci, and, through successive acquisitions, developed as the besylate salt at CeNeS and PAION. The development of remimazolam besylate has been slow by industry standards, primarily because of the resource limitations of these small companies. It has, however, recently been approved for anesthesia in Japan and South Korea, procedural sedation in the United States, China, and Europe, and for compassionate use in intensive care unit sedation in Belgium. A second development program of remimazolam was later initiated in China, using a slightly different salt form, remimazolam tosylate. This salt form of the compound has also recently been approved for procedural sedation in China. Remimazolam has the pharmacological profile of a classical benzodiazepine, such as midazolam, but is differentiated from other intravenous benzodiazepines by its rapid conversion to an inactive metabolite resulting in a short onset/offset profile. It is differentiated from other intravenous hypnotic agents, such as propofol, by its low liability for cardiovascular depression, respiratory depression, and injection pain. The benzodiazepine antagonist flumazenil can reverse the effects of remimazolam in case of adverse events and further shorten recovery times. The aim of this review is to provide an analysis of, and perspective on, published non-clinical and clinical information on 1) the pharmacology, metabolism, pharmacokinetics, and pharmacodynamic profile of remimazolam, 2) the profile of remimazolam compared with established agents, 3) gaps in the current understanding of remimazolam, 4) the compound's discovery and development process and 5) likely future developments in the clinical use of remimazolam.
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页数:18
相关论文
共 141 条
[1]   The Effectiveness of Midazolam for Preventing Postoperative Nausea and Vomiting: A Systematic Review and Meta-Analysis [J].
Ahn, Eun Jin ;
Kang, Hyun ;
Choi, Geun Joo ;
Baek, Chong Wha ;
Jung, Yong Hun ;
Woo, Young Choel .
ANESTHESIA AND ANALGESIA, 2016, 122 (03) :664-676
[2]   A Placebo- and Midazolam-Controlled Phase I Single Ascending-Dose Study Evaluating the Safety, Pharmacokinetics, and Pharmacodynamics of Remimazolam (CNS 7056): Part I. Safety, Efficacy, and Basic Pharmacokinetics [J].
Antonik, Laurie J. ;
Goldwater, D. Ronald ;
Kilpatrick, Gavin J. ;
Tilbrook, Gary S. ;
Borkett, Keith M. .
ANESTHESIA AND ANALGESIA, 2012, 115 (02) :274-283
[3]   Clinical Practice Guidelines for the Management of Pain, Agitation, and Delirium in Adult Patients in the Intensive Care Unit [J].
Barr, Juliana ;
Fraser, Gilles L. ;
Puntillo, Kathleen ;
Ely, E. Wesley ;
Gelinas, Celine ;
Dasta, Joseph F. ;
Davidson, Judy E. ;
Devlin, John W. ;
Kress, John P. ;
Davidson, Judy E. ;
Devlin, John W. ;
Kress, John P. ;
Joffe, Aaron M. ;
Coursin, Douglas B. ;
Herr, Daniel L. ;
Tung, Avery ;
Robinson, Bryce R. H. ;
Fontaine, Dorrie K. ;
Ramsay, Michael A. ;
Riker, Richard R. ;
Sessler, Curtis N. ;
Pun, Brenda ;
Skrobik, Yoanna ;
Jaeschke, Roman .
CRITICAL CARE MEDICINE, 2013, 41 (01) :263-306
[4]   PROLONGED SEDATION DUE TO ACCUMULATION OF CONJUGATED METABOLITES OF MIDAZOLAM [J].
BAUER, TM ;
RITZ, R ;
HABERTHUR, C ;
HA, HR ;
HUNKELER, W ;
SLEIGHT, AJ ;
SCOLLOLAVIZZARI, G ;
HAEFELI, WE .
LANCET, 1995, 346 (8968) :145-147
[5]   Inhaled Remimazolam Potentiates Inhaled Remifentanil in Rodents [J].
Bevans, Tatjana ;
Deering-Rice, Cassandra ;
Stockmann, Chris ;
Rower, Joseph ;
Sakata, Derek ;
Reilly, Christopher .
ANESTHESIA AND ANALGESIA, 2017, 124 (05) :1484-1490
[6]  
Bevilacqua C, 2015, J CARDIOTHOR VASC AN, V29, pS50, DOI [10.1053/j.jvca.2015.05.267, DOI 10.1053/J.JVCA.2015.05.267]
[7]   Soft drugs in anesthesia: remifentanil as prototype to modern anesthetic drug development [J].
Birgenheier, Nathaniel M. ;
Stuart, Ami R. ;
Egan, Talmage D. .
CURRENT OPINION IN ANESTHESIOLOGY, 2020, 33 (04) :499-505
[8]   A Phase IIa, Randomized, Double-Blind Study of Remimazolam (CNS 7056) Versus Midazolam for Sedation in Upper Gastrointestinal Endoscopy [J].
Borkett, Keith M. ;
Riff, Dennis S. ;
Schwartz, Howard I. ;
Winkle, Peter J. ;
Pambianco, Daniel J. ;
Lees, James P. ;
Wilhelm-Ogunbiyi, Karin .
ANESTHESIA AND ANALGESIA, 2015, 120 (04) :771-780
[9]   Bispectral index monitoring of sedation during endoscopy [J].
Bower, AL ;
Ripepi, A ;
Dilger, J ;
Boparai, N ;
Brody, FJ ;
Ponsky, JL .
GASTROINTESTINAL ENDOSCOPY, 2000, 52 (02) :192-196
[10]  
Bray RJ, 1998, PAEDIATR ANAESTH, V8, P491