Drug intelligence / Profile preview

sufentanil + dexketoprofen tromethamine

Development stage
Preclinical
Lead developer
Talphera
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules
Administration
Intravenous, Epidural, Intrathecal, Oral, Intramuscular, Sublingual
01

Overview

This is a combination drug consisting of sufentanil, a potent synthetic opioid analgesic, and dexketoprofen tromethamine (also known as dexketoprofen trometamol), a non-steroidal anti-inflammatory drug (NSAID). Sufentanil acts primarily as an agonist at the mu-opioid receptor, providing strong analgesia and sedation. It is used for induction and maintenance of anesthesia, management of severe acute pain, and in some settings for labor analgesia[3]. Dexketoprofen tromethamine is the S(+)-enantiomer of ketoprofen formulated as a water-soluble salt; it inhibits both COX-1 and COX-2 enzymes to reduce prostaglandin synthesis, resulting in analgesic, anti-inflammatory, and antipyretic effects[4][6][8]. The combination aims to provide synergistic or supra-additive pain relief by targeting different mechanisms—central opioid pathways (sufentanil) and peripheral/central prostaglandin-mediated pathways (dexketoprofen)[1][2]. This multimodal approach may allow lower doses of each component with improved efficacy and potentially fewer side effects compared to higher doses of either agent alone.

02

Targets

MOR (Mu opioid receptor)PTGS2 (Prostaglandin-Endoperoxide Synthase 2)PGHS-1 (Prostaglandin G/H Synthase 1)

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